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Items: 1 to 20 of 8467

1.

rs1491544172 [Homo sapiens]
    Variant type:
    INS
    Alleles:
    ->A,ATA,ATATA,ATATATA,ATATATATA,ATATATATATA,ATATATATATATA,ATATATATATATATA,ATATATATATATATATATA,ATATATATATC [Show Flanks]
    Chromosome:
    19:54744955 (GRCh38)
    19:55256408 (GRCh37)
    Canonical SPDI:
    NC_000019.10:54744955::A,NC_000019.10:54744955::ATA,NC_000019.10:54744955::ATATA,NC_000019.10:54744955::ATATATA,NC_000019.10:54744955::ATATATATA,NC_000019.10:54744955::ATATATATATA,NC_000019.10:54744955::ATATATATATATA,NC_000019.10:54744955::ATATATATATATATA,NC_000019.10:54744955::ATATATATATATATATATA,NC_000019.10:54744955::ATATATATATC
    Gene:
    KIR2DL3 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    ATA=0./0 (ALFA)
    ATATATATATATATATATA=0.000004/1 (TOPMED)
    HGVS:
    NC_000019.10:g.54744955_54744956insA, NC_000019.10:g.54744955_54744956insATA, NC_000019.10:g.54744955_54744956insATATA, NC_000019.10:g.54744955_54744956insATATATA, NC_000019.10:g.54744955_54744956insATATATATA, NC_000019.10:g.54744955_54744956insATATATATATA, NC_000019.10:g.54744955_54744956insATATATATATATA, NC_000019.10:g.54744955_54744956insATATATATATATATA, NC_000019.10:g.54744955_54744956insATATATATATATATATATA, NC_000019.10:g.54744955_54744956insATATATATATC, NW_004166865.1:g.719322_719323insA, NW_004166865.1:g.719322_719323insATA, NW_004166865.1:g.719322_719323insATATA, NW_004166865.1:g.719322_719323insATATATA, NW_004166865.1:g.719322_719323insATATATATA, NW_004166865.1:g.719322_719323insATATATATATA, NW_004166865.1:g.719322_719323insATATATATATATA, NW_004166865.1:g.719322_719323insATATATATATATATA, NW_004166865.1:g.719322_719323insATATATATATATATATATA, NW_004166865.1:g.719322_719323insATATATATATC, NG_046935.1:g.11447_11448insA, NG_046935.1:g.11447_11448insATA, NG_046935.1:g.11447_11448insATATA, NG_046935.1:g.11447_11448insATATATA, NG_046935.1:g.11447_11448insATATATATA, NG_046935.1:g.11447_11448insATATATATATA, NG_046935.1:g.11447_11448insATATATATATATA, NG_046935.1:g.11447_11448insATATATATATATATA, NG_046935.1:g.11447_11448insATATATATATATATATATA, NG_046935.1:g.11447_11448insATATATATATC, NW_016107308.1:g.46543dup, NW_016107308.1:g.46543_46545dup, NW_016107308.1:g.46543_46546AT[2]AATAT[1], NW_016107308.1:g.46543_46546AT[3]AATAT[1], NW_016107308.1:g.46543_46546AT[4]AATAT[1], NW_016107308.1:g.46543_46546AT[5]AATAT[1], NW_016107308.1:g.46543_46546AT[6]AATAT[1], NW_016107308.1:g.46543_46546AT[7]AATAT[1], NW_016107308.1:g.46543_46546AT[9]AATAT[1], NW_016107308.1:g.46543_46546AT[5]CATAT[1], NT_187673.1:g.124122_124123insT, NT_187673.1:g.124122_124123insTAT, NT_187673.1:g.124122_124123insTATAT, NT_187673.1:g.124122_124123insTATATAT, NT_187673.1:g.124122_124123insTATATATAT, NT_187673.1:g.124122_124123insTATATATATAT, NT_187673.1:g.124122_124123insTATATATATATAT, NT_187673.1:g.124122_124123insTATATATATATATAT, NT_187673.1:g.124122_124123insTATATATATATATATATAT, NT_187673.1:g.124122_124123insGATATATATAT, NW_016107313.1:g.46584_46585insA, NW_016107313.1:g.46584_46585insATA, NW_016107313.1:g.46584_46585insATATA, NW_016107313.1:g.46584_46585insATATATA, NW_016107313.1:g.46584_46585insATATATATA, NW_016107313.1:g.46584_46585insATATATATATA, NW_016107313.1:g.46584_46585insATATATATATATA, NW_016107313.1:g.46584_46585insATATATATATATATA, NW_016107313.1:g.46584_46585insATATATATATATATATATA, NW_016107313.1:g.46584_46585insATATATATATC, NW_016107305.1:g.46551_46552insA, NW_016107305.1:g.46551_46552insATA, NW_016107305.1:g.46551_46552insATATA, NW_016107305.1:g.46551_46552insATATATA, NW_016107305.1:g.46551_46552insATATATATA, NW_016107305.1:g.46551_46552insATATATATATA, NW_016107305.1:g.46551_46552insATATATATATATA, NW_016107305.1:g.46551_46552insATATATATATATATA, NW_016107305.1:g.46551_46552insATATATATATATATATATA, NW_016107305.1:g.46551_46552insATATATATATC, NT_187687.1:g.123945_123946insT, NT_187687.1:g.123945_123946insTAT, NT_187687.1:g.123945_123946insTATAT, NT_187687.1:g.123945_123946insTATATAT, NT_187687.1:g.123945_123946insTATATATAT, NT_187687.1:g.123945_123946insTATATATATAT, NT_187687.1:g.123945_123946insTATATATATATAT, NT_187687.1:g.123945_123946insTATATATATATATAT, NT_187687.1:g.123945_123946insTATATATATATATATATAT, NT_187687.1:g.123945_123946insGATATATATAT, NT_187674.1:g.31794_31795insA, NT_187674.1:g.31794_31795insATA, NT_187674.1:g.31794_31795insATATA, NT_187674.1:g.31794_31795insATATATA, NT_187674.1:g.31794_31795insATATATATA, NT_187674.1:g.31794_31795insATATATATATA, NT_187674.1:g.31794_31795insATATATATATATA, NT_187674.1:g.31794_31795insATATATATATATATA, NT_187674.1:g.31794_31795insATATATATATATATATATA, NT_187674.1:g.31794_31795insATATATATATC, NW_016107302.1:g.46564_46565insA, NW_016107302.1:g.46564_46565insATA, NW_016107302.1:g.46564_46565insATATA, NW_016107302.1:g.46564_46565insATATATA, NW_016107302.1:g.46564_46565insATATATATA, NW_016107302.1:g.46564_46565insATATATATATA, NW_016107302.1:g.46564_46565insATATATATATATA, NW_016107302.1:g.46564_46565insATATATATATATATA, NW_016107302.1:g.46564_46565insATATATATATATATATATA, NW_016107302.1:g.46564_46565insATATATATATC, NW_003571054.1:g.650615_650616insA, NW_003571054.1:g.650615_650616insATA, NW_003571054.1:g.650615_650616insATATA, NW_003571054.1:g.650615_650616insATATATA, NW_003571054.1:g.650615_650616insATATATATA, NW_003571054.1:g.650615_650616insATATATATATA, NW_003571054.1:g.650615_650616insATATATATATATA, NW_003571054.1:g.650615_650616insATATATATATATATA, NW_003571054.1:g.650615_650616insATATATATATATATATATA, NW_003571054.1:g.650615_650616insATATATATATC, NT_187683.1:g.19132_19133insA, NT_187683.1:g.19132_19133insATA, NT_187683.1:g.19132_19133insATATA, NT_187683.1:g.19132_19133insATATATA, NT_187683.1:g.19132_19133insATATATATA, NT_187683.1:g.19132_19133insATATATATATA, NT_187683.1:g.19132_19133insATATATATATATA, NT_187683.1:g.19132_19133insATATATATATATATA, NT_187683.1:g.19132_19133insATATATATATATATATATA, NT_187683.1:g.19132_19133insATATATATATC, NW_016107301.1:g.46588_46589insA, NW_016107301.1:g.46588_46589insATA, NW_016107301.1:g.46588_46589insATATA, NW_016107301.1:g.46588_46589insATATATA, NW_016107301.1:g.46588_46589insATATATATA, NW_016107301.1:g.46588_46589insATATATATATA, NW_016107301.1:g.46588_46589insATATATATATATA, NW_016107301.1:g.46588_46589insATATATATATATATA, NW_016107301.1:g.46588_46589insATATATATATATATATATA, NW_016107301.1:g.46588_46589insATATATATATC, NW_016107309.1:g.46562_46563insA, NW_016107309.1:g.46562_46563insATA, NW_016107309.1:g.46562_46563insATATA, NW_016107309.1:g.46562_46563insATATATA, NW_016107309.1:g.46562_46563insATATATATA, NW_016107309.1:g.46562_46563insATATATATATA, NW_016107309.1:g.46562_46563insATATATATATATA, NW_016107309.1:g.46562_46563insATATATATATATATA, NW_016107309.1:g.46562_46563insATATATATATATATATATA, NW_016107309.1:g.46562_46563insATATATATATC, NW_016107300.1:g.46573_46574insA, NW_016107300.1:g.46573_46574insATA, NW_016107300.1:g.46573_46574insATATA, NW_016107300.1:g.46573_46574insATATATA, NW_016107300.1:g.46573_46574insATATATATA, NW_016107300.1:g.46573_46574insATATATATATA, NW_016107300.1:g.46573_46574insATATATATATATA, NW_016107300.1:g.46573_46574insATATATATATATATA, NW_016107300.1:g.46573_46574insATATATATATATATATATA, NW_016107300.1:g.46573_46574insATATATATATC, NW_016107307.1:g.46523dup, NW_016107307.1:g.46523_46525dup, NW_016107307.1:g.46523_46527dup, NW_016107307.1:g.46523_46528AT[3]AATATAT[1], NW_016107307.1:g.46523_46528AT[4]AATATAT[1], NW_016107307.1:g.46523_46528AT[5]AATATAT[1], NW_016107307.1:g.46523_46528AT[6]AATATAT[1], NW_016107307.1:g.46523_46528AT[7]AATATAT[1], NW_016107307.1:g.46523_46528AT[9]AATATAT[1], NW_016107307.1:g.46523_46528AT[5]CATATAT[1], NT_187672.1:g.46527dup, NT_187672.1:g.46527_46529dup, NT_187672.1:g.46527_46531dup, NT_187672.1:g.46527_46533dup, NT_187672.1:g.46527_46535dup, NT_187672.1:g.46527_46536AT[5]AATATATATAT[1], NT_187672.1:g.46527_46536AT[6]AATATATATAT[1], NT_187672.1:g.46527_46536AT[7]AATATATATAT[1], NT_187672.1:g.46527_46536AT[9]AATATATATAT[1], NT_187672.1:g.46527_46536AT[5]CATATATATAT[1], NT_187671.1:g.23863dup, NT_187671.1:g.23863_23865dup, NT_187671.1:g.23863_23867dup, NT_187671.1:g.23863_23869dup, NT_187671.1:g.23863_23871dup, NT_187671.1:g.23863_23872AT[5]AATATATATAT[1], NT_187671.1:g.23863_23872AT[6]AATATATATAT[1], NT_187671.1:g.23863_23872AT[7]AATATATATAT[1], NT_187671.1:g.23863_23872AT[9]AATATATATAT[1], NT_187671.1:g.23863_23872AT[5]CATATATATAT[1], NW_016107304.1:g.46558dup, NW_016107304.1:g.46558_46560dup, NW_016107304.1:g.46558_46562dup, NW_016107304.1:g.46558_46564dup, NW_016107304.1:g.46558_46566dup, NW_016107304.1:g.46558_46567AT[5]AATATATATAT[1], NW_016107304.1:g.46558_46567AT[6]AATATATATAT[1], NW_016107304.1:g.46558_46567AT[7]AATATATATAT[1], NW_016107304.1:g.46558_46567AT[9]AATATATATAT[1], NW_016107304.1:g.46558_46567AT[5]CATATATATAT[1], NT_187643.1:g.124141_124142insT, NT_187643.1:g.124141_124142insTAT, NT_187643.1:g.124141_124142insTATAT, NT_187643.1:g.124141_124142insTATATAT, NT_187643.1:g.124141_124142insTATATATAT, NT_187643.1:g.124141_124142insTATATATATAT, NT_187643.1:g.124141_124142insTATATATATATAT, NT_187643.1:g.124141_124142insTATATATATATATAT, NT_187643.1:g.124141_124142insTATATATATATATATATAT, NT_187643.1:g.124141_124142insGATATATATAT, NT_187641.1:g.163467_163468insT, NT_187641.1:g.163467_163468insTAT, NT_187641.1:g.163467_163468insTATAT, NT_187641.1:g.163467_163468insTATATAT, NT_187641.1:g.163467_163468insTATATATAT, NT_187641.1:g.163467_163468insTATATATATAT, NT_187641.1:g.163467_163468insTATATATATATAT, NT_187641.1:g.163467_163468insTATATATATATATAT, NT_187641.1:g.163467_163468insTATATATATATATATATAT, NT_187641.1:g.163467_163468insGATATATATAT, NT_187645.1:g.124160_124161insT, NT_187645.1:g.124160_124161insTAT, NT_187645.1:g.124160_124161insTATAT, NT_187645.1:g.124160_124161insTATATAT, NT_187645.1:g.124160_124161insTATATATAT, NT_187645.1:g.124160_124161insTATATATATAT, NT_187645.1:g.124160_124161insTATATATATATAT, NT_187645.1:g.124160_124161insTATATATATATATAT, NT_187645.1:g.124160_124161insTATATATATATATATATAT, NT_187645.1:g.124160_124161insGATATATATAT, NT_187685.1:g.123630_123631insT, NT_187685.1:g.123630_123631insTAT, NT_187685.1:g.123630_123631insTATAT, NT_187685.1:g.123630_123631insTATATAT, NT_187685.1:g.123630_123631insTATATATAT, NT_187685.1:g.123630_123631insTATATATATAT, NT_187685.1:g.123630_123631insTATATATATATAT, NT_187685.1:g.123630_123631insTATATATATATATAT, NT_187685.1:g.123630_123631insTATATATATATATATATAT, NT_187685.1:g.123630_123631insGATATATATAT, NW_003571061.2:g.487182dup, NW_003571061.2:g.487182_487184dup, NW_003571061.2:g.487182_487186dup, NW_003571061.2:g.487182_487188dup, NW_003571061.2:g.487182_487190dup, NW_003571061.2:g.487182_487192dup, NW_003571061.2:g.487182_487193AT[6]AATATATATATAT[1], NW_003571061.2:g.487182_487193AT[7]AATATATATATAT[1], NW_003571061.2:g.487182_487193AT[9]AATATATATATAT[1], NW_003571061.2:g.487182_487191AT[5]CATATATATAT[1], NW_003571061.1:g.487181dup, NW_003571061.1:g.487181_487183dup, NW_003571061.1:g.487181_487185dup, NW_003571061.1:g.487181_487187dup, NW_003571061.1:g.487181_487189dup, NW_003571061.1:g.487181_487191dup, NW_003571061.1:g.487181_487192AT[6]AATATATATATAT[1], NW_003571061.1:g.487181_487192AT[7]AATATATATATAT[1], NW_003571061.1:g.487181_487192AT[9]AATATATATATAT[1], NW_003571061.1:g.487181_487190AT[5]CATATATATAT[1], NW_003571056.2:g.743855dup, NW_003571056.2:g.743855_743857dup, NW_003571056.2:g.743855_743859dup, NW_003571056.2:g.743855_743860AT[3]AATATAT[1], NW_003571056.2:g.743855_743860AT[4]AATATAT[1], NW_003571056.2:g.743855_743860AT[5]AATATAT[1], NW_003571056.2:g.743855_743860AT[6]AATATAT[1], NW_003571056.2:g.743855_743860AT[7]AATATAT[1], NW_003571056.2:g.743855_743860AT[9]AATATAT[1], NW_003571056.2:g.743855_743860AT[5]CATATAT[1], NW_003571056.1:g.743854dup, NW_003571056.1:g.743854_743856dup, NW_003571056.1:g.743854_743858dup, NW_003571056.1:g.743854_743859AT[3]AATATAT[1], NW_003571056.1:g.743854_743859AT[4]AATATAT[1], NW_003571056.1:g.743854_743859AT[5]AATATAT[1], NW_003571056.1:g.743854_743859AT[6]AATATAT[1], NW_003571056.1:g.743854_743859AT[7]AATATAT[1], NW_003571056.1:g.743854_743859AT[9]AATATAT[1], NW_003571056.1:g.743854_743859AT[5]CATATAT[1], NT_187668.1:g.142446dup, NT_187668.1:g.142444_142446dup, NT_187668.1:g.142442_142446dup, NT_187668.1:g.142441_142446AT[3]TA[3]T[1], NT_187668.1:g.142441_142446AT[3]TA[4]T[1], NT_187668.1:g.142441_142446AT[3]TA[5]T[1], NT_187668.1:g.142441_142446AT[3]TA[6]T[1], NT_187668.1:g.142441_142446AT[3]TA[7]T[1], NT_187668.1:g.142441_142446AT[3]TA[9]T[1], NT_187668.1:g.142441_142446AT[3]GATATATATAT[1], NT_187638.1:g.94263dup, NT_187638.1:g.94261_94263dup, NT_187638.1:g.94259_94263dup, NT_187638.1:g.94257_94263dup, NT_187638.1:g.94255_94263dup, NT_187638.1:g.94253_94263dup, NT_187638.1:g.94252_94263AT[6]TA[6]T[1], NT_187638.1:g.94252_94263AT[6]TA[7]T[1], NT_187638.1:g.94252_94263AT[6]TA[9]T[1], NT_187638.1:g.94254_94263AT[5]GATATATATAT[1], NT_187642.1:g.92783dup, NT_187642.1:g.92781_92783dup, NT_187642.1:g.92779_92783dup, NT_187642.1:g.92777_92783dup, NT_187642.1:g.92776_92783AT[4]TA[4]T[1], NT_187642.1:g.92776_92783AT[4]TA[5]T[1], NT_187642.1:g.92776_92783AT[4]TA[6]T[1], NT_187642.1:g.92776_92783AT[4]TA[7]T[1], NT_187642.1:g.92776_92783AT[4]TA[9]T[1], NT_187642.1:g.92776_92783AT[4]GATATATATAT[1], NC_000019.9:g.55256408dup, NC_000019.9:g.55256409_55256410insAAT, NC_000019.9:g.55256408_55256409AT[2]AAT[1], NC_000019.9:g.55256408_55256409AT[3]AAT[1], NC_000019.9:g.55256408_55256409AT[4]AAT[1], NC_000019.9:g.55256408_55256409AT[5]AAT[1], NC_000019.9:g.55256408_55256409AT[6]AAT[1], NC_000019.9:g.55256408_55256409AT[7]AAT[1], NC_000019.9:g.55256408_55256409AT[9]AAT[1], NC_000019.9:g.55256408_55256409AT[5]CAT[1]

    2.

    rs1491375451 [Homo sapiens]
      Variant type:
      DEL
      Alleles:
      TG>- [Show Flanks]
      Chromosome:
      19:54737224 (GRCh38)
      19:55248689 (GRCh37)
      Canonical SPDI:
      NC_000019.10:54737223:TG:
      Gene:
      KIR2DL3 (Varview)
      Functional Consequence:
      2KB_upstream_variant,upstream_transcript_variant
      Validated:
      by frequency,by alfa
      MAF:
      -=0./0 (ALFA)
      HGVS:
      NC_000019.10:g.54737224_54737225del, NW_004166865.1:g.711591_711592del, NG_046935.1:g.3716_3717del, NG_050568.1:g.17778_17779del, NW_003571059.2:g.720062_720063del, NW_003571059.1:g.720061_720062del, NW_003571057.2:g.825969_825970del, NW_003571057.1:g.825968_825969del, NT_113949.2:g.138561dup, NT_113949.2:g.138550del, NW_003571061.2:g.463267_463268del, NW_003571061.1:g.463266_463267del, NW_016107308.1:g.38811_38812del, NT_187673.1:g.131853_131854del, NW_016107313.1:g.38844_38845del, NW_016107305.1:g.38812_38813del, NT_187687.1:g.131684_131685del, NT_187674.1:g.24029_24030del, NW_016107302.1:g.38818_38819del, NW_003571054.1:g.642869_642870del, NT_187683.1:g.11401_11402del, NW_016107301.1:g.38845_38846del, NT_187639.1:g.132175_132176del, NW_016107309.1:g.38846_38847del, NW_016107300.1:g.38852_38853del, NW_016107307.1:g.38810_38811del, NW_016107303.1:g.38812_38813del, NT_187693.1:g.719803_719804del, NC_000019.9:g.55248689_55248690del, NT_187672.1:g.38810_38811del, NT_187671.1:g.16146_16147del, NW_016107304.1:g.38845_38846del, NT_187643.1:g.131868dup, NT_187643.1:g.131853del, NT_187676.1:g.13159_13160del, NT_187641.1:g.171193dup, NT_187641.1:g.171179del, NT_187637.1:g.131609dup, NT_187637.1:g.131595del, NW_003571060.1:g.641574_641575del, NT_187645.1:g.131884dup, NT_187645.1:g.131871del, NT_187685.1:g.131354dup, NT_187685.1:g.131340del, NT_187669.1:g.131862dup, NT_187669.1:g.131848del, NW_016107311.1:g.38830_38831del, NT_187684.1:g.161919dup, NT_187684.1:g.161909del, NT_187686.1:g.176869dup, NT_187686.1:g.176858del, NT_187638.1:g.118189dup, NT_187638.1:g.118178del, NT_187644.1:g.145628dup, NT_187644.1:g.145617del, NT_187668.1:g.166373dup, NT_187668.1:g.166362del, NT_187670.1:g.145716dup, NT_187670.1:g.145705del, NT_187642.1:g.116710dup, NT_187642.1:g.116699del, NW_016107306.1:g.38829_38830del, NT_187677.1:g.28207_28208del, NW_016107314.1:g.38831_38832del, NT_187675.1:g.35764_35765del, NT_187636.1:g.209993dup, NT_187636.1:g.209982del, NT_187640.1:g.165420dup, NT_187640.1:g.165409del, NW_003571056.2:g.736121_736122del, NW_003571056.1:g.736120_736121del, NT_113949.1:g.20619_20620del

      3.

      rs1491290011 has merged into rs1185648350 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        TATATATATATATATATATA>-,TA,TATATA,TATATATA,TATATATATA,TATATATATATA,TATATATATATATA,TATATATATATATATA,TATATATATATATATATA,TATATATATATATATATATATA,TATATATATATATATATATATATA,TATATATATATATATATATATATATA,TATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATATA [Show Flanks]
        Chromosome:
        19:54744879 (GRCh38)
        19:55256327 (GRCh37)
        Canonical SPDI:
        NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000019.10:54744870:TATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA
        Gene:
        KIR2DL3 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        TATATATA=0./0 (ALFA)
        HGVS:
        NC_000019.10:g.54744871TA[4], NC_000019.10:g.54744871TA[5], NC_000019.10:g.54744871TA[7], NC_000019.10:g.54744871TA[8], NC_000019.10:g.54744871TA[9], NC_000019.10:g.54744871TA[10], NC_000019.10:g.54744871TA[11], NC_000019.10:g.54744871TA[12], NC_000019.10:g.54744871TA[13], NC_000019.10:g.54744871TA[15], NC_000019.10:g.54744871TA[16], NC_000019.10:g.54744871TA[17], NC_000019.10:g.54744871TA[18], NC_000019.10:g.54744871TA[19], NC_000019.10:g.54744871TA[20], NC_000019.10:g.54744871TA[21], NC_000019.10:g.54744871TA[22], NC_000019.10:g.54744871TA[23], NC_000019.10:g.54744871TA[24], NC_000019.10:g.54744871TA[25], NC_000019.10:g.54744871TA[26], NC_000019.10:g.54744871TA[27], NC_000019.10:g.54744871TA[28], NC_000019.10:g.54744871TA[29], NC_000019.10:g.54744871TA[30], NW_004166865.1:g.719238TA[4], NW_004166865.1:g.719238TA[5], NW_004166865.1:g.719238TA[7], NW_004166865.1:g.719238TA[8], NW_004166865.1:g.719238TA[9], NW_004166865.1:g.719238TA[10], NW_004166865.1:g.719238TA[11], NW_004166865.1:g.719238TA[12], NW_004166865.1:g.719238TA[13], NW_004166865.1:g.719238TA[15], NW_004166865.1:g.719238TA[16], NW_004166865.1:g.719238TA[17], NW_004166865.1:g.719238TA[18], NW_004166865.1:g.719238TA[19], NW_004166865.1:g.719238TA[20], NW_004166865.1:g.719238TA[21], NW_004166865.1:g.719238TA[22], NW_004166865.1:g.719238TA[23], NW_004166865.1:g.719238TA[24], NW_004166865.1:g.719238TA[25], NW_004166865.1:g.719238TA[26], NW_004166865.1:g.719238TA[27], NW_004166865.1:g.719238TA[28], NW_004166865.1:g.719238TA[29], NW_004166865.1:g.719238TA[30], NG_046935.1:g.11363TA[4], NG_046935.1:g.11363TA[5], NG_046935.1:g.11363TA[7], NG_046935.1:g.11363TA[8], NG_046935.1:g.11363TA[9], NG_046935.1:g.11363TA[10], NG_046935.1:g.11363TA[11], NG_046935.1:g.11363TA[12], NG_046935.1:g.11363TA[13], NG_046935.1:g.11363TA[15], NG_046935.1:g.11363TA[16], NG_046935.1:g.11363TA[17], NG_046935.1:g.11363TA[18], NG_046935.1:g.11363TA[19], NG_046935.1:g.11363TA[20], NG_046935.1:g.11363TA[21], NG_046935.1:g.11363TA[22], NG_046935.1:g.11363TA[23], NG_046935.1:g.11363TA[24], NG_046935.1:g.11363TA[25], NG_046935.1:g.11363TA[26], NG_046935.1:g.11363TA[27], NG_046935.1:g.11363TA[28], NG_046935.1:g.11363TA[29], NG_046935.1:g.11363TA[30], NW_003571059.2:g.727709TA[4], NW_003571059.2:g.727709TA[5], NW_003571059.2:g.727709TA[7], NW_003571059.2:g.727709TA[8], NW_003571059.2:g.727709TA[9], NW_003571059.2:g.727709TA[10], NW_003571059.2:g.727709TA[11], NW_003571059.2:g.727709TA[12], NW_003571059.2:g.727709TA[13], NW_003571059.2:g.727709TA[15], NW_003571059.2:g.727709TA[16], NW_003571059.2:g.727709TA[17], NW_003571059.2:g.727709TA[18], NW_003571059.2:g.727709TA[19], NW_003571059.2:g.727709TA[20], NW_003571059.2:g.727709TA[21], NW_003571059.2:g.727709TA[22], NW_003571059.2:g.727709TA[23], NW_003571059.2:g.727709TA[24], NW_003571059.2:g.727709TA[25], NW_003571059.2:g.727709TA[26], NW_003571059.2:g.727709TA[27], NW_003571059.2:g.727709TA[28], NW_003571059.2:g.727709TA[29], NW_003571059.2:g.727709TA[30], NW_003571059.1:g.727708TA[4], NW_003571059.1:g.727708TA[5], NW_003571059.1:g.727708TA[7], NW_003571059.1:g.727708TA[8], NW_003571059.1:g.727708TA[9], NW_003571059.1:g.727708TA[10], NW_003571059.1:g.727708TA[11], NW_003571059.1:g.727708TA[12], NW_003571059.1:g.727708TA[13], NW_003571059.1:g.727708TA[15], NW_003571059.1:g.727708TA[16], NW_003571059.1:g.727708TA[17], NW_003571059.1:g.727708TA[18], NW_003571059.1:g.727708TA[19], NW_003571059.1:g.727708TA[20], NW_003571059.1:g.727708TA[21], NW_003571059.1:g.727708TA[22], NW_003571059.1:g.727708TA[23], NW_003571059.1:g.727708TA[24], NW_003571059.1:g.727708TA[25], NW_003571059.1:g.727708TA[26], NW_003571059.1:g.727708TA[27], NW_003571059.1:g.727708TA[28], NW_003571059.1:g.727708TA[29], NW_003571059.1:g.727708TA[30], NW_016107308.1:g.46458TA[4], NW_016107308.1:g.46458TA[5], NW_016107308.1:g.46458TA[7], NW_016107308.1:g.46458TA[8], NW_016107308.1:g.46458TA[9], NW_016107308.1:g.46458TA[10], NW_016107308.1:g.46458TA[11], NW_016107308.1:g.46458TA[12], NW_016107308.1:g.46458TA[13], NW_016107308.1:g.46458TA[15], NW_016107308.1:g.46458TA[16], NW_016107308.1:g.46458TA[17], NW_016107308.1:g.46458TA[18], NW_016107308.1:g.46458TA[19], NW_016107308.1:g.46458TA[20], NW_016107308.1:g.46458TA[21], NW_016107308.1:g.46458TA[22], NW_016107308.1:g.46458TA[23], NW_016107308.1:g.46458TA[24], NW_016107308.1:g.46458TA[25], NW_016107308.1:g.46458TA[26], NW_016107308.1:g.46458TA[27], NW_016107308.1:g.46458TA[28], NW_016107308.1:g.46458TA[29], NW_016107308.1:g.46458TA[30], NT_187673.1:g.124180TA[4], NT_187673.1:g.124180TA[5], NT_187673.1:g.124180TA[7], NT_187673.1:g.124180TA[8], NT_187673.1:g.124180TA[9], NT_187673.1:g.124180TA[10], NT_187673.1:g.124180TA[11], NT_187673.1:g.124180TA[12], NT_187673.1:g.124180TA[13], NT_187673.1:g.124180TA[15], NT_187673.1:g.124180TA[16], NT_187673.1:g.124180TA[17], NT_187673.1:g.124180TA[18], NT_187673.1:g.124180TA[19], NT_187673.1:g.124180TA[20], NT_187673.1:g.124180TA[21], NT_187673.1:g.124180TA[22], NT_187673.1:g.124180TA[23], NT_187673.1:g.124180TA[24], NT_187673.1:g.124180TA[25], NT_187673.1:g.124180TA[26], NT_187673.1:g.124180TA[27], NT_187673.1:g.124180TA[28], NT_187673.1:g.124180TA[29], NT_187673.1:g.124180TA[30], NW_016107313.1:g.46489TA[4], NW_016107313.1:g.46489TA[5], NW_016107313.1:g.46489TA[7], NW_016107313.1:g.46489TA[8], NW_016107313.1:g.46489TA[9], NW_016107313.1:g.46489TA[10], NW_016107313.1:g.46489TA[11], NW_016107313.1:g.46489TA[12], NW_016107313.1:g.46489TA[13], NW_016107313.1:g.46489TA[15], NW_016107313.1:g.46489TA[16], NW_016107313.1:g.46489TA[17], NW_016107313.1:g.46489TA[18], NW_016107313.1:g.46489TA[19], NW_016107313.1:g.46489TA[20], NW_016107313.1:g.46489TA[21], NW_016107313.1:g.46489TA[22], NW_016107313.1:g.46489TA[23], NW_016107313.1:g.46489TA[24], NW_016107313.1:g.46489TA[25], NW_016107313.1:g.46489TA[26], NW_016107313.1:g.46489TA[27], NW_016107313.1:g.46489TA[28], NW_016107313.1:g.46489TA[29], NW_016107313.1:g.46489TA[30], NW_016107305.1:g.46457TA[4], NW_016107305.1:g.46457TA[5], NW_016107305.1:g.46457TA[7], NW_016107305.1:g.46457TA[8], NW_016107305.1:g.46457TA[9], NW_016107305.1:g.46457TA[10], NW_016107305.1:g.46457TA[11], NW_016107305.1:g.46457TA[12], NW_016107305.1:g.46457TA[13], NW_016107305.1:g.46457TA[15], NW_016107305.1:g.46457TA[16], NW_016107305.1:g.46457TA[17], NW_016107305.1:g.46457TA[18], NW_016107305.1:g.46457TA[19], NW_016107305.1:g.46457TA[20], NW_016107305.1:g.46457TA[21], NW_016107305.1:g.46457TA[22], NW_016107305.1:g.46457TA[23], NW_016107305.1:g.46457TA[24], NW_016107305.1:g.46457TA[25], NW_016107305.1:g.46457TA[26], NW_016107305.1:g.46457TA[27], NW_016107305.1:g.46457TA[28], NW_016107305.1:g.46457TA[29], NW_016107305.1:g.46457TA[30], NT_187687.1:g.124014G>A, NT_187687.1:g.124014_124033del, NT_187687.1:g.124014_124031del, NT_187687.1:g.124014_124027del, NT_187687.1:g.124014_124025del, NT_187687.1:g.124014_124023del, NT_187687.1:g.124014_124021del, NT_187687.1:g.124014_124019del, NT_187687.1:g.124014_124017del, NT_187687.1:g.124002GT[6], NT_187687.1:g.124014delinsATA, NT_187687.1:g.124014delinsATATA, NT_187687.1:g.124014delinsATATATA, NT_187687.1:g.124014delinsATATATATA, NT_187687.1:g.124014delinsATATATATATA, NT_187687.1:g.124014delinsATATATATATATA, NT_187687.1:g.124014delinsATATATATATATATA, NT_187687.1:g.124014delinsATATATATATATATATA, NT_187687.1:g.124014delinsATATATATATATATATATA, NT_187687.1:g.124014delinsATATATATATATATATATATA, NT_187687.1:g.124014delinsATATATATATATATATATATATA, NT_187687.1:g.124014delinsATATATATATATATATATATATATA, NT_187687.1:g.124014delinsATATATATATATATATATATATATATA, NT_187687.1:g.124014delinsATATATATATATATATATATATATATATA, NT_187687.1:g.124014delinsATATATATATATATATATATATATATATATA, NT_187687.1:g.124014delinsATATATATATATATATATATATATATATATATA, NT_187674.1:g.31676TA[18], NT_187674.1:g.31676TA[19], NT_187674.1:g.31676TA[21], NT_187674.1:g.31676TA[22], NT_187674.1:g.31676TA[23], NT_187674.1:g.31676TA[24], NT_187674.1:g.31676TA[25], NT_187674.1:g.31676TA[26], NT_187674.1:g.31676TA[27], NT_187674.1:g.31676TA[29], NT_187674.1:g.31676TA[30], NT_187674.1:g.31676TA[31], NT_187674.1:g.31676TA[32], NT_187674.1:g.31676TA[33], NT_187674.1:g.31676TA[34], NT_187674.1:g.31676TA[35], NT_187674.1:g.31676TA[36], NT_187674.1:g.31676TA[37], NT_187674.1:g.31676TA[38], NT_187674.1:g.31676TA[39], NT_187674.1:g.31676TA[40], NT_187674.1:g.31676TA[41], NT_187674.1:g.31676TA[42], NT_187674.1:g.31676TA[43], NT_187674.1:g.31676TA[44], NW_016107302.1:g.46463TA[11], NW_016107302.1:g.46463TA[12], NW_016107302.1:g.46463TA[14], NW_016107302.1:g.46463TA[15], NW_016107302.1:g.46463TA[16], NW_016107302.1:g.46463TA[17], NW_016107302.1:g.46463TA[18], NW_016107302.1:g.46463TA[19], NW_016107302.1:g.46463TA[20], NW_016107302.1:g.46463TA[22], NW_016107302.1:g.46463TA[23], NW_016107302.1:g.46463TA[24], NW_016107302.1:g.46463TA[25], NW_016107302.1:g.46463TA[26], NW_016107302.1:g.46463TA[27], NW_016107302.1:g.46463TA[28], 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NT_187643.1:g.124199TA[12], NT_187643.1:g.124199TA[13], NT_187643.1:g.124199TA[15], NT_187643.1:g.124199TA[16], NT_187643.1:g.124199TA[17], NT_187643.1:g.124199TA[18], NT_187643.1:g.124199TA[19], NT_187643.1:g.124199TA[20], NT_187643.1:g.124199TA[21], NT_187643.1:g.124199TA[22], NT_187643.1:g.124199TA[23], NT_187643.1:g.124199TA[24], NT_187643.1:g.124199TA[25], NT_187643.1:g.124199TA[26], NT_187643.1:g.124199TA[27], NT_187643.1:g.124199TA[28], NT_187643.1:g.124199TA[29], NT_187643.1:g.124199TA[30], NT_187676.1:g.20787TA[4], NT_187676.1:g.20787TA[5], NT_187676.1:g.20787TA[7], NT_187676.1:g.20787TA[8], NT_187676.1:g.20787TA[9], NT_187676.1:g.20787TA[10], NT_187676.1:g.20787TA[11], NT_187676.1:g.20787TA[12], NT_187676.1:g.20787TA[13], NT_187676.1:g.20787TA[15], NT_187676.1:g.20787TA[16], NT_187676.1:g.20787TA[17], NT_187676.1:g.20787TA[18], NT_187676.1:g.20787TA[19], NT_187676.1:g.20787TA[20], NT_187676.1:g.20787TA[21], NT_187676.1:g.20787TA[22], NT_187676.1:g.20787TA[23], NT_187676.1:g.20787TA[24], NT_187676.1:g.20787TA[25], NT_187676.1:g.20787TA[26], NT_187676.1:g.20787TA[27], NT_187676.1:g.20787TA[28], NT_187676.1:g.20787TA[29], NT_187676.1:g.20787TA[30], NT_187641.1:g.163525TA[4], NT_187641.1:g.163525TA[5], NT_187641.1:g.163525TA[7], NT_187641.1:g.163525TA[8], NT_187641.1:g.163525TA[9], NT_187641.1:g.163525TA[10], NT_187641.1:g.163525TA[11], NT_187641.1:g.163525TA[12], NT_187641.1:g.163525TA[13], NT_187641.1:g.163525TA[15], NT_187641.1:g.163525TA[16], NT_187641.1:g.163525TA[17], NT_187641.1:g.163525TA[18], NT_187641.1:g.163525TA[19], NT_187641.1:g.163525TA[20], NT_187641.1:g.163525TA[21], NT_187641.1:g.163525TA[22], NT_187641.1:g.163525TA[23], NT_187641.1:g.163525TA[24], NT_187641.1:g.163525TA[25], NT_187641.1:g.163525TA[26], NT_187641.1:g.163525TA[27], NT_187641.1:g.163525TA[28], NT_187641.1:g.163525TA[29], NT_187641.1:g.163525TA[30], NT_187637.1:g.123943TA[14], NT_187637.1:g.123943TA[4], NT_187637.1:g.123943TA[5], NT_187637.1:g.123943TA[7], NT_187637.1:g.123943TA[8], NT_187637.1:g.123943TA[9], NT_187637.1:g.123943TA[10], NT_187637.1:g.123943TA[11], NT_187637.1:g.123943TA[12], NT_187637.1:g.123943TA[15], NT_187637.1:g.123943TA[16], NT_187637.1:g.123943TA[17], NT_187637.1:g.123943TA[18], NT_187637.1:g.123943TA[19], NT_187637.1:g.123943TA[20], NT_187637.1:g.123943TA[21], NT_187637.1:g.123943TA[22], NT_187637.1:g.123943TA[23], NT_187637.1:g.123943TA[24], NT_187637.1:g.123943TA[25], NT_187637.1:g.123943TA[26], NT_187637.1:g.123943TA[27], NT_187637.1:g.123943TA[28], NT_187637.1:g.123943TA[29], NT_187637.1:g.123943TA[30], NW_003571060.1:g.649201TA[14], NW_003571060.1:g.649201TA[4], NW_003571060.1:g.649201TA[5], NW_003571060.1:g.649201TA[7], NW_003571060.1:g.649201TA[8], NW_003571060.1:g.649201TA[9], NW_003571060.1:g.649201TA[10], NW_003571060.1:g.649201TA[11], NW_003571060.1:g.649201TA[12], NW_003571060.1:g.649201TA[15], NW_003571060.1:g.649201TA[16], NW_003571060.1:g.649201TA[17], NW_003571060.1:g.649201TA[18], NW_003571060.1:g.649201TA[19], NW_003571060.1:g.649201TA[20], NW_003571060.1:g.649201TA[21], NW_003571060.1:g.649201TA[22], NW_003571060.1:g.649201TA[23], NW_003571060.1:g.649201TA[24], NW_003571060.1:g.649201TA[25], NW_003571060.1:g.649201TA[26], NW_003571060.1:g.649201TA[27], NW_003571060.1:g.649201TA[28], NW_003571060.1:g.649201TA[29], NW_003571060.1:g.649201TA[30], NT_187645.1:g.124217TA[4], NT_187645.1:g.124217TA[5], NT_187645.1:g.124217TA[7], NT_187645.1:g.124217TA[8], NT_187645.1:g.124217TA[9], NT_187645.1:g.124217TA[10], NT_187645.1:g.124217TA[11], NT_187645.1:g.124217TA[12], NT_187645.1:g.124217TA[13], NT_187645.1:g.124217TA[15], NT_187645.1:g.124217TA[16], NT_187645.1:g.124217TA[17], NT_187645.1:g.124217TA[18], NT_187645.1:g.124217TA[19], NT_187645.1:g.124217TA[20], NT_187645.1:g.124217TA[21], NT_187645.1:g.124217TA[22], NT_187645.1:g.124217TA[23], NT_187645.1:g.124217TA[24], NT_187645.1:g.124217TA[25], NT_187645.1:g.124217TA[26], NT_187645.1:g.124217TA[27], NT_187645.1:g.124217TA[28], NT_187645.1:g.124217TA[29], NT_187645.1:g.124217TA[30], NT_187685.1:g.123688TA[14], NT_187685.1:g.123688TA[4], NT_187685.1:g.123688TA[5], NT_187685.1:g.123688TA[7], NT_187685.1:g.123688TA[8], NT_187685.1:g.123688TA[9], NT_187685.1:g.123688TA[10], NT_187685.1:g.123688TA[11], NT_187685.1:g.123688TA[12], NT_187685.1:g.123688TA[15], NT_187685.1:g.123688TA[16], NT_187685.1:g.123688TA[17], NT_187685.1:g.123688TA[18], NT_187685.1:g.123688TA[19], NT_187685.1:g.123688TA[20], NT_187685.1:g.123688TA[21], NT_187685.1:g.123688TA[22], NT_187685.1:g.123688TA[23], NT_187685.1:g.123688TA[24], NT_187685.1:g.123688TA[25], NT_187685.1:g.123688TA[26], NT_187685.1:g.123688TA[27], NT_187685.1:g.123688TA[28], NT_187685.1:g.123688TA[29], NT_187685.1:g.123688TA[30], NT_187669.1:g.124194TA[4], NT_187669.1:g.124194TA[5], NT_187669.1:g.124194TA[7], NT_187669.1:g.124194TA[8], NT_187669.1:g.124194TA[9], NT_187669.1:g.124194TA[10], NT_187669.1:g.124194TA[11], NT_187669.1:g.124194TA[12], NT_187669.1:g.124194TA[13], NT_187669.1:g.124194TA[15], NT_187669.1:g.124194TA[16], NT_187669.1:g.124194TA[17], NT_187669.1:g.124194TA[18], NT_187669.1:g.124194TA[19], NT_187669.1:g.124194TA[20], NT_187669.1:g.124194TA[21], NT_187669.1:g.124194TA[22], NT_187669.1:g.124194TA[23], NT_187669.1:g.124194TA[24], NT_187669.1:g.124194TA[25], NT_187669.1:g.124194TA[26], NT_187669.1:g.124194TA[27], NT_187669.1:g.124194TA[28], NT_187669.1:g.124194TA[29], NT_187669.1:g.124194TA[30], NW_016107311.1:g.46487_46498delinsATATATATATATA, NW_016107311.1:g.46480_46498del, NW_016107311.1:g.46482_46498del, NW_016107311.1:g.46486_46498del, NW_016107311.1:g.46487_46498delinsA, NW_016107311.1:g.46487_46498delinsATA, NW_016107311.1:g.46487_46498delinsATATA, NW_016107311.1:g.46487_46498delinsATATATA, NW_016107311.1:g.46487_46498delinsATATATATA, NW_016107311.1:g.46487_46498delinsATATATATATA, NW_016107311.1:g.46487_46498delinsATATATATATATATA, NW_016107311.1:g.46487_46498delinsATATATATATATATATA, NW_016107311.1:g.46487_46498delinsATATATATATATATATATA, NW_016107311.1:g.46487_46498delinsATATATATATATATATATATA, NW_016107311.1:g.46487_46498delinsATATATATATATATATATATATA, NW_016107311.1:g.46487_46498delinsATATATATATATATATATATATATA, NW_016107311.1:g.46487_46498delinsATATATATATATATATATATATATATA, NW_016107311.1:g.46487_46498delinsATATATATATATATATATATATATATATA, NW_016107311.1:g.46487_46498delinsATATATATATATATATATATATATATATATA, NW_016107311.1:g.46487_46498delinsATATATATATATATATATATATATATATATATA, NW_016107311.1:g.46487_46498delinsATATATATATATATATATATATATATATATATATA, NW_016107311.1:g.46487_46498delinsATATATATATATATATATATATATATATATATATATA, NW_016107311.1:g.46487_46498delinsATATATATATATATATATATATATATATATATATATATA, NW_016107311.1:g.46487_46498delinsATATATATATATATATATATATATATATATATATATATATA, NW_016107311.1:g.46487_46498delinsATATATATATATATATATATATATATATATATATATATATATA, NW_016107311.1:g.46487_46498delinsATATATATATATATATATATATATATATATATATATATATATATA, NW_016107306.1:g.46341AT[14], NW_016107306.1:g.46341AT[4], NW_016107306.1:g.46341AT[5], NW_016107306.1:g.46341AT[8], NW_016107306.1:g.46341AT[9], NW_016107306.1:g.46341AT[10], NW_016107306.1:g.46341AT[11], NW_016107306.1:g.46341AT[12], NW_016107306.1:g.46341AT[13], NW_016107306.1:g.46341AT[15], NW_016107306.1:g.46341AT[16], NW_016107306.1:g.46341AT[17], NW_016107306.1:g.46341AT[18], NW_016107306.1:g.46341AT[19], NW_016107306.1:g.46341AT[20], NW_016107306.1:g.46341AT[21], NW_016107306.1:g.46341AT[22], NW_016107306.1:g.46341AT[23], NW_016107306.1:g.46341AT[24], NW_016107306.1:g.46341AT[25], NW_016107306.1:g.46341AT[26], NW_016107306.1:g.46341AT[27], NW_016107306.1:g.46341AT[28], NW_016107306.1:g.46341AT[29], NW_016107306.1:g.46341AT[30], NT_187677.1:g.52020TA[8], NT_187677.1:g.52020TA[9], NT_187677.1:g.52020TA[11], NT_187677.1:g.52020TA[12], NT_187677.1:g.52020TA[13], NT_187677.1:g.52020TA[14], NT_187677.1:g.52020TA[15], NT_187677.1:g.52020TA[16], NT_187677.1:g.52020TA[17], NT_187677.1:g.52020TA[19], NT_187677.1:g.52020TA[20], NT_187677.1:g.52020TA[21], NT_187677.1:g.52020TA[22], NT_187677.1:g.52020TA[23], NT_187677.1:g.52020TA[24], NT_187677.1:g.52020TA[25], NT_187677.1:g.52020TA[26], NT_187677.1:g.52020TA[27], NT_187677.1:g.52020TA[28], NT_187677.1:g.52020TA[29], NT_187677.1:g.52020TA[30], NT_187677.1:g.52020TA[31], NT_187677.1:g.52020TA[32], NT_187677.1:g.52020TA[33], NT_187677.1:g.52020TA[34]

        4.

        rs1491261405 [Homo sapiens]
          Variant type:
          SNV:
          Alleles:
          ->TTTTA
          Chromosome:
          no mapping
          Canonical SPDI:

          5.

          rs1491235497 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            ->AATA [Show Flanks]
            Chromosome:
            19:54744871 (GRCh38)
            19:55256320 (GRCh37)
            Canonical SPDI:
            NC_000019.10:54744871:ATA:ATAAATA
            Gene:
            KIR2DL3 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa
            MAF:
            ATAAATA=0.00211/25 (ALFA)
            HGVS:
            NC_000019.10:g.54744874_54744875insAATA, NW_004166865.1:g.719241_719242insAATA, NG_046935.1:g.11366_11367insAATA, NW_003571059.2:g.727712_727713insAATA, NW_003571059.1:g.727711_727712insAATA, NW_016107308.1:g.46461_46462insAATA, NT_187673.1:g.124206_124207insTTAT, NW_016107313.1:g.46492_46493insAATA, NW_016107305.1:g.46460_46461insAATA, NT_187687.1:g.124039_124040insTTAT, NT_187674.1:g.31707_31708insAATA, NW_016107302.1:g.46480_46481insAATA, NW_003571054.1:g.650529_650530insAATA, NT_187683.1:g.19046_19047insAATA, NW_016107301.1:g.46509_46510insAATA, NT_187639.1:g.124528_124529insTTAT, NW_016107309.1:g.46481_46482insAATA, NW_016107300.1:g.46490_46491insAATA, NW_016107307.1:g.46441_46442insAATA, NW_016107303.1:g.46449_46450insAATA, NT_187693.1:g.727436_727437insAATA, NC_000019.9:g.55256322_55256323insAATA, NT_187672.1:g.46445_46446insAATA, NT_187671.1:g.23781_23782insAATA, NW_016107304.1:g.46476_46477insAATA, NT_187643.1:g.124225_124226insTTAT, NT_187676.1:g.20790_20791insAATA, NT_187641.1:g.163551_163552insTTAT, NT_187637.1:g.123967_123968insTTAT, NW_003571060.1:g.649200_649201insA, NW_003571060.1:g.649200_649201insATAAA, NT_187645.1:g.124243_124244insTTAT, NT_187685.1:g.123712_123713insTTAT, NT_187669.1:g.124220_124221insTTAT, NW_016107311.1:g.46475_46476insAATA, NT_187684.1:g.154271_154272insTTAT, NW_003571061.2:g.487077_487080dup, NW_003571061.1:g.487076_487079dup, NW_003571056.2:g.743750_743753dup, NW_003571056.1:g.743749_743752dup, NT_113949.2:g.131037_131038insTTAT, NT_187675.1:g.59573_59576dup, NW_016107306.1:g.46343_46344insAATA, NT_187636.1:g.186174_186177dup, NT_187677.1:g.52025_52026insAATA, NT_187686.1:g.153050_153053dup, NT_187668.1:g.142553_142556dup, NT_187640.1:g.141601_141604dup, NT_187638.1:g.94370_94373dup, NT_187670.1:g.138193_138194insTTAT, NT_187644.1:g.138105_138106insTTAT, NT_187642.1:g.92890_92893dup

            6.

            rs1491220357 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              ->CATA [Show Flanks]
              Chromosome:
              19:54776238 (GRCh38)
              19:55287691 (GRCh37)
              Canonical SPDI:
              NC_000019.10:54776238:ATA:ATACATA
              Gene:
              KIR2DL1 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              ATACATA=0.000084/1 (ALFA)
              ATAC=0.000069/8 (GnomAD)
              ATAC=0.000142/4 (TOMMO)
              HGVS:
              NC_000019.10:g.54776241_54776242insCATA, NW_004166865.1:g.750609_750610insCATA, NG_051369.1:g.12034_12035insCATA, NW_016107309.1:g.77848_77849insCATA, NW_016107307.1:g.77808_77809insCATA, NW_016107304.1:g.77851_77852insCATA, NW_016107303.1:g.77819_77820insCATA, NW_016107300.1:g.77874_77875insCATA, NW_003571060.1:g.680575_680576insCATA, NT_187693.1:g.758807_758808insCATA, NC_000019.9:g.55287693_55287694insCATA, NT_187685.1:g.92352_92353insGTAT, NT_187676.1:g.52155_52156insCATA, NT_187673.1:g.92839_92840insGTAT, NT_187672.1:g.77819_77820insCATA, NT_187669.1:g.92860_92861insGTAT, NT_187645.1:g.92876_92877insGTAT, NT_187643.1:g.92860_92861insGTAT, NT_187641.1:g.132186_132187insGTAT, NT_187639.1:g.93169_93170insGTAT, NT_187637.1:g.92600_92601insGTAT, NT_187671.1:g.55154_55155insCATA, NW_016107305.1:g.77835_77836insCATA, NW_016107301.1:g.77879_77880insCATA, NW_003571054.1:g.681899_681900insCATA, NT_187687.1:g.92664_92665insGTAT, NT_187683.1:g.50417_50418insCATA, NT_187674.1:g.63078_63079insCATA, NW_016107306.1:g.77654_77657dup, NW_016107302.1:g.77848_77849insCATA, NT_187686.1:g.93206_93209dup, NT_187684.1:g.94352_94355dup, NT_187675.1:g.119240_119243dup, NT_187668.1:g.82761_82762insGTAT, NT_187640.1:g.81970_81973dup, NT_187636.1:g.126510_126513dup, NT_113949.2:g.114643_114644insGTAT, NT_113949.1:g.28349_28350insCATA, NW_016107313.1:g.77866_77867insCATA, NT_187670.1:g.121813_121814insGTAT, NT_187644.1:g.121721_121722insGTAT, NW_016107310.1:g.108223_108226dup, NW_016107311.1:g.77840_77841insCATA

              7.

              rs1491215885 has merged into rs71195797 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                TTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                Chromosome:
                19:54744961 (GRCh38)
                19:55256414 (GRCh37)
                Canonical SPDI:
                NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54744954:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                Gene:
                KIR2DL3 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                TTTTTT=0./0 (ALFA)
                -=0.038/6 (NorthernSweden)
                HGVS:
                NC_000019.10:g.54744961_54744977del, NC_000019.10:g.54744962_54744977del, NC_000019.10:g.54744963_54744977del, NC_000019.10:g.54744964_54744977del, NC_000019.10:g.54744965_54744977del, NC_000019.10:g.54744966_54744977del, NC_000019.10:g.54744967_54744977del, NC_000019.10:g.54744968_54744977del, NC_000019.10:g.54744969_54744977del, NC_000019.10:g.54744970_54744977del, NC_000019.10:g.54744971_54744977del, NC_000019.10:g.54744972_54744977del, NC_000019.10:g.54744973_54744977del, NC_000019.10:g.54744974_54744977del, NC_000019.10:g.54744975_54744977del, NC_000019.10:g.54744976_54744977del, NC_000019.10:g.54744977del, NC_000019.10:g.54744977dup, NC_000019.10:g.54744976_54744977dup, NC_000019.10:g.54744975_54744977dup, NC_000019.10:g.54744974_54744977dup, NC_000019.10:g.54744973_54744977dup, NC_000019.10:g.54744972_54744977dup, NC_000019.10:g.54744971_54744977dup, NC_000019.10:g.54744970_54744977dup, NC_000019.10:g.54744969_54744977dup, NC_000019.10:g.54744968_54744977dup, NC_000019.10:g.54744967_54744977dup, NW_004166865.1:g.719328_719344del, NW_004166865.1:g.719329_719344del, NW_004166865.1:g.719330_719344del, NW_004166865.1:g.719331_719344del, NW_004166865.1:g.719332_719344del, NW_004166865.1:g.719333_719344del, NW_004166865.1:g.719334_719344del, NW_004166865.1:g.719335_719344del, NW_004166865.1:g.719336_719344del, NW_004166865.1:g.719337_719344del, NW_004166865.1:g.719338_719344del, NW_004166865.1:g.719339_719344del, NW_004166865.1:g.719340_719344del, NW_004166865.1:g.719341_719344del, NW_004166865.1:g.719342_719344del, NW_004166865.1:g.719343_719344del, NW_004166865.1:g.719344del, NW_004166865.1:g.719344dup, NW_004166865.1:g.719343_719344dup, NW_004166865.1:g.719342_719344dup, NW_004166865.1:g.719341_719344dup, NW_004166865.1:g.719340_719344dup, NW_004166865.1:g.719339_719344dup, NW_004166865.1:g.719338_719344dup, NW_004166865.1:g.719337_719344dup, NW_004166865.1:g.719336_719344dup, NW_004166865.1:g.719335_719344dup, NW_004166865.1:g.719334_719344dup, NG_046935.1:g.11453_11469del, NG_046935.1:g.11454_11469del, NG_046935.1:g.11455_11469del, NG_046935.1:g.11456_11469del, NG_046935.1:g.11457_11469del, NG_046935.1:g.11458_11469del, NG_046935.1:g.11459_11469del, NG_046935.1:g.11460_11469del, NG_046935.1:g.11461_11469del, NG_046935.1:g.11462_11469del, NG_046935.1:g.11463_11469del, NG_046935.1:g.11464_11469del, NG_046935.1:g.11465_11469del, NG_046935.1:g.11466_11469del, NG_046935.1:g.11467_11469del, NG_046935.1:g.11468_11469del, NG_046935.1:g.11469del, NG_046935.1:g.11469dup, NG_046935.1:g.11468_11469dup, NG_046935.1:g.11467_11469dup, NG_046935.1:g.11466_11469dup, NG_046935.1:g.11465_11469dup, NG_046935.1:g.11464_11469dup, NG_046935.1:g.11463_11469dup, NG_046935.1:g.11462_11469dup, NG_046935.1:g.11461_11469dup, NG_046935.1:g.11460_11469dup, NG_046935.1:g.11459_11469dup, NW_003571059.2:g.727812_727813dup, NW_003571059.2:g.727799_727813del, NW_003571059.2:g.727800_727813del, NW_003571059.2:g.727801_727813del, NW_003571059.2:g.727802_727813del, NW_003571059.2:g.727803_727813del, NW_003571059.2:g.727804_727813del, NW_003571059.2:g.727805_727813del, NW_003571059.2:g.727806_727813del, NW_003571059.2:g.727807_727813del, NW_003571059.2:g.727808_727813del, NW_003571059.2:g.727809_727813del, NW_003571059.2:g.727810_727813del, NW_003571059.2:g.727811_727813del, NW_003571059.2:g.727812_727813del, NW_003571059.2:g.727813del, NW_003571059.2:g.727813dup, NW_003571059.2:g.727811_727813dup, NW_003571059.2:g.727810_727813dup, NW_003571059.2:g.727809_727813dup, NW_003571059.2:g.727808_727813dup, NW_003571059.2:g.727807_727813dup, NW_003571059.2:g.727806_727813dup, NW_003571059.2:g.727805_727813dup, NW_003571059.2:g.727804_727813dup, NW_003571059.2:g.727803_727813dup, NW_003571059.2:g.727802_727813dup, NW_003571059.2:g.727801_727813dup, NT_187673.1:g.124107_124123del, NT_187673.1:g.124108_124123del, NT_187673.1:g.124109_124123del, NT_187673.1:g.124110_124123del, NT_187673.1:g.124111_124123del, NT_187673.1:g.124112_124123del, NT_187673.1:g.124113_124123del, NT_187673.1:g.124114_124123del, NT_187673.1:g.124115_124123del, NT_187673.1:g.124116_124123del, NT_187673.1:g.124117_124123del, NT_187673.1:g.124118_124123del, NT_187673.1:g.124119_124123del, NT_187673.1:g.124120_124123del, NT_187673.1:g.124121_124123del, NT_187673.1:g.124122_124123del, NT_187673.1:g.124123del, NT_187673.1:g.124123dup, NT_187673.1:g.124122_124123dup, NT_187673.1:g.124121_124123dup, NT_187673.1:g.124120_124123dup, NT_187673.1:g.124119_124123dup, NT_187673.1:g.124118_124123dup, NT_187673.1:g.124117_124123dup, NT_187673.1:g.124116_124123dup, NT_187673.1:g.124115_124123dup, NT_187673.1:g.124114_124123dup, NT_187673.1:g.124113_124123dup, NW_016107313.1:g.46590_46606del, NW_016107313.1:g.46591_46606del, NW_016107313.1:g.46592_46606del, NW_016107313.1:g.46593_46606del, NW_016107313.1:g.46594_46606del, NW_016107313.1:g.46595_46606del, NW_016107313.1:g.46596_46606del, NW_016107313.1:g.46597_46606del, NW_016107313.1:g.46598_46606del, NW_016107313.1:g.46599_46606del, NW_016107313.1:g.46600_46606del, NW_016107313.1:g.46601_46606del, NW_016107313.1:g.46602_46606del, NW_016107313.1:g.46603_46606del, NW_016107313.1:g.46604_46606del, NW_016107313.1:g.46605_46606del, NW_016107313.1:g.46606del, NW_016107313.1:g.46606dup, NW_016107313.1:g.46605_46606dup, NW_016107313.1:g.46604_46606dup, NW_016107313.1:g.46603_46606dup, NW_016107313.1:g.46602_46606dup, NW_016107313.1:g.46601_46606dup, NW_016107313.1:g.46600_46606dup, NW_016107313.1:g.46599_46606dup, NW_016107313.1:g.46598_46606dup, NW_016107313.1:g.46597_46606dup, NW_016107313.1:g.46596_46606dup, NW_016107305.1:g.46557_46573del, NW_016107305.1:g.46558_46573del, NW_016107305.1:g.46559_46573del, NW_016107305.1:g.46560_46573del, NW_016107305.1:g.46561_46573del, NW_016107305.1:g.46562_46573del, NW_016107305.1:g.46563_46573del, NW_016107305.1:g.46564_46573del, NW_016107305.1:g.46565_46573del, NW_016107305.1:g.46566_46573del, NW_016107305.1:g.46567_46573del, NW_016107305.1:g.46568_46573del, NW_016107305.1:g.46569_46573del, NW_016107305.1:g.46570_46573del, NW_016107305.1:g.46571_46573del, NW_016107305.1:g.46572_46573del, NW_016107305.1:g.46573del, NW_016107305.1:g.46573dup, NW_016107305.1:g.46572_46573dup, NW_016107305.1:g.46571_46573dup, NW_016107305.1:g.46570_46573dup, NW_016107305.1:g.46569_46573dup, NW_016107305.1:g.46568_46573dup, NW_016107305.1:g.46567_46573dup, NW_016107305.1:g.46566_46573dup, NW_016107305.1:g.46565_46573dup, NW_016107305.1:g.46564_46573dup, NW_016107305.1:g.46563_46573dup, NT_187687.1:g.123930_123946del, NT_187687.1:g.123931_123946del, NT_187687.1:g.123932_123946del, NT_187687.1:g.123933_123946del, NT_187687.1:g.123934_123946del, NT_187687.1:g.123935_123946del, NT_187687.1:g.123936_123946del, NT_187687.1:g.123937_123946del, NT_187687.1:g.123938_123946del, NT_187687.1:g.123939_123946del, NT_187687.1:g.123940_123946del, NT_187687.1:g.123941_123946del, NT_187687.1:g.123942_123946del, NT_187687.1:g.123943_123946del, NT_187687.1:g.123944_123946del, NT_187687.1:g.123945_123946del, NT_187687.1:g.123946del, NT_187687.1:g.123946dup, NT_187687.1:g.123945_123946dup, NT_187687.1:g.123944_123946dup, NT_187687.1:g.123943_123946dup, NT_187687.1:g.123942_123946dup, NT_187687.1:g.123941_123946dup, NT_187687.1:g.123940_123946dup, NT_187687.1:g.123939_123946dup, NT_187687.1:g.123938_123946dup, NT_187687.1:g.123937_123946dup, NT_187687.1:g.123936_123946dup, NT_187674.1:g.31800_31816del, NT_187674.1:g.31801_31816del, NT_187674.1:g.31802_31816del, NT_187674.1:g.31803_31816del, NT_187674.1:g.31804_31816del, NT_187674.1:g.31805_31816del, NT_187674.1:g.31806_31816del, NT_187674.1:g.31807_31816del, NT_187674.1:g.31808_31816del, NT_187674.1:g.31809_31816del, NT_187674.1:g.31810_31816del, NT_187674.1:g.31811_31816del, NT_187674.1:g.31812_31816del, NT_187674.1:g.31813_31816del, NT_187674.1:g.31814_31816del, NT_187674.1:g.31815_31816del, NT_187674.1:g.31816del, NT_187674.1:g.31816dup, NT_187674.1:g.31815_31816dup, NT_187674.1:g.31814_31816dup, NT_187674.1:g.31813_31816dup, NT_187674.1:g.31812_31816dup, NT_187674.1:g.31811_31816dup, NT_187674.1:g.31810_31816dup, NT_187674.1:g.31809_31816dup, NT_187674.1:g.31808_31816dup, NT_187674.1:g.31807_31816dup, NT_187674.1:g.31806_31816dup, NW_016107302.1:g.46570_46586del, NW_016107302.1:g.46571_46586del, NW_016107302.1:g.46572_46586del, NW_016107302.1:g.46573_46586del, NW_016107302.1:g.46574_46586del, NW_016107302.1:g.46575_46586del, NW_016107302.1:g.46576_46586del, NW_016107302.1:g.46577_46586del, NW_016107302.1:g.46578_46586del, NW_016107302.1:g.46579_46586del, NW_016107302.1:g.46580_46586del, NW_016107302.1:g.46581_46586del, NW_016107302.1:g.46582_46586del, NW_016107302.1:g.46583_46586del, NW_016107302.1:g.46584_46586del, NW_016107302.1:g.46585_46586del, NW_016107302.1:g.46586del, NW_016107302.1:g.46586dup, NW_016107302.1:g.46585_46586dup, NW_016107302.1:g.46584_46586dup, NW_016107302.1:g.46583_46586dup, NW_016107302.1:g.46582_46586dup, NW_016107302.1:g.46581_46586dup, NW_016107302.1:g.46580_46586dup, NW_016107302.1:g.46579_46586dup, NW_016107302.1:g.46578_46586dup, NW_016107302.1:g.46577_46586dup, NW_016107302.1:g.46576_46586dup, NW_003571054.1:g.650621_650637del, NW_003571054.1:g.650622_650637del, NW_003571054.1:g.650623_650637del, NW_003571054.1:g.650624_650637del, NW_003571054.1:g.650625_650637del, NW_003571054.1:g.650626_650637del, NW_003571054.1:g.650627_650637del, NW_003571054.1:g.650628_650637del, NW_003571054.1:g.650629_650637del, NW_003571054.1:g.650630_650637del, NW_003571054.1:g.650631_650637del, NW_003571054.1:g.650632_650637del, NW_003571054.1:g.650633_650637del, NW_003571054.1:g.650634_650637del, NW_003571054.1:g.650635_650637del, NW_003571054.1:g.650636_650637del, NW_003571054.1:g.650637del, NW_003571054.1:g.650637dup, NW_003571054.1:g.650636_650637dup, NW_003571054.1:g.650635_650637dup, NW_003571054.1:g.650634_650637dup, NW_003571054.1:g.650633_650637dup, NW_003571054.1:g.650632_650637dup, NW_003571054.1:g.650631_650637dup, NW_003571054.1:g.650630_650637dup, NW_003571054.1:g.650629_650637dup, NW_003571054.1:g.650628_650637dup, NW_003571054.1:g.650627_650637dup, NT_187683.1:g.19138_19154del, NT_187683.1:g.19139_19154del, NT_187683.1:g.19140_19154del, NT_187683.1:g.19141_19154del, NT_187683.1:g.19142_19154del, NT_187683.1:g.19143_19154del, NT_187683.1:g.19144_19154del, NT_187683.1:g.19145_19154del, NT_187683.1:g.19146_19154del, NT_187683.1:g.19147_19154del, NT_187683.1:g.19148_19154del, NT_187683.1:g.19149_19154del, NT_187683.1:g.19150_19154del, NT_187683.1:g.19151_19154del, NT_187683.1:g.19152_19154del, NT_187683.1:g.19153_19154del, NT_187683.1:g.19154del, NT_187683.1:g.19154dup, NT_187683.1:g.19153_19154dup, NT_187683.1:g.19152_19154dup, NT_187683.1:g.19151_19154dup, NT_187683.1:g.19150_19154dup, NT_187683.1:g.19149_19154dup, NT_187683.1:g.19148_19154dup, NT_187683.1:g.19147_19154dup, NT_187683.1:g.19146_19154dup, NT_187683.1:g.19145_19154dup, NT_187683.1:g.19144_19154dup, NW_016107301.1:g.46600_46616del, NW_016107301.1:g.46601_46616del, NW_016107301.1:g.46602_46616del, NW_016107301.1:g.46603_46616del, NW_016107301.1:g.46604_46616del, NW_016107301.1:g.46605_46616del, NW_016107301.1:g.46606_46616del, NW_016107301.1:g.46607_46616del, NW_016107301.1:g.46608_46616del, NW_016107301.1:g.46609_46616del, NW_016107301.1:g.46610_46616del, NW_016107301.1:g.46611_46616del, NW_016107301.1:g.46612_46616del, NW_016107301.1:g.46613_46616del, NW_016107301.1:g.46614_46616del, NW_016107301.1:g.46615_46616del, NW_016107301.1:g.46616del, NW_016107301.1:g.46616dup, NW_016107301.1:g.46615_46616dup, NW_016107301.1:g.46614_46616dup, NW_016107301.1:g.46613_46616dup, NW_016107301.1:g.46612_46616dup, NW_016107301.1:g.46611_46616dup, NW_016107301.1:g.46610_46616dup, NW_016107301.1:g.46609_46616dup, NW_016107301.1:g.46608_46616dup, NW_016107301.1:g.46607_46616dup, NW_016107301.1:g.46606_46616dup, NT_187639.1:g.124449_124451dup, NT_187639.1:g.124438_124451del, NT_187639.1:g.124439_124451del, NT_187639.1:g.124440_124451del, NT_187639.1:g.124441_124451del, NT_187639.1:g.124442_124451del, NT_187639.1:g.124443_124451del, NT_187639.1:g.124444_124451del, NT_187639.1:g.124445_124451del, NT_187639.1:g.124446_124451del, NT_187639.1:g.124447_124451del, NT_187639.1:g.124448_124451del, NT_187639.1:g.124449_124451del, NT_187639.1:g.124450_124451del, NT_187639.1:g.124451del, NT_187639.1:g.124451dup, NT_187639.1:g.124450_124451dup, NT_187639.1:g.124448_124451dup, NT_187639.1:g.124447_124451dup, NT_187639.1:g.124446_124451dup, NT_187639.1:g.124445_124451dup, NT_187639.1:g.124444_124451dup, NT_187639.1:g.124443_124451dup, NT_187639.1:g.124442_124451dup, NT_187639.1:g.124441_124451dup, NT_187639.1:g.124440_124451dup, NT_187639.1:g.124439_124451dup, NT_187639.1:g.124438_124451dup, NW_016107309.1:g.46568_46584del, NW_016107309.1:g.46569_46584del, NW_016107309.1:g.46570_46584del, NW_016107309.1:g.46571_46584del, NW_016107309.1:g.46572_46584del, NW_016107309.1:g.46573_46584del, NW_016107309.1:g.46574_46584del, NW_016107309.1:g.46575_46584del, NW_016107309.1:g.46576_46584del, NW_016107309.1:g.46577_46584del, NW_016107309.1:g.46578_46584del, NW_016107309.1:g.46579_46584del, NW_016107309.1:g.46580_46584del, NW_016107309.1:g.46581_46584del, NW_016107309.1:g.46582_46584del, NW_016107309.1:g.46583_46584del, NW_016107309.1:g.46584del, NW_016107309.1:g.46584dup, NW_016107309.1:g.46583_46584dup, NW_016107309.1:g.46582_46584dup, NW_016107309.1:g.46581_46584dup, NW_016107309.1:g.46580_46584dup, NW_016107309.1:g.46579_46584dup, NW_016107309.1:g.46578_46584dup, NW_016107309.1:g.46577_46584dup, NW_016107309.1:g.46576_46584dup, NW_016107309.1:g.46575_46584dup, NW_016107309.1:g.46574_46584dup, NW_016107300.1:g.46579_46595del, NW_016107300.1:g.46580_46595del, NW_016107300.1:g.46581_46595del, NW_016107300.1:g.46582_46595del, NW_016107300.1:g.46583_46595del, NW_016107300.1:g.46584_46595del, NW_016107300.1:g.46585_46595del, NW_016107300.1:g.46586_46595del, NW_016107300.1:g.46587_46595del, NW_016107300.1:g.46588_46595del, NW_016107300.1:g.46589_46595del, NW_016107300.1:g.46590_46595del, NW_016107300.1:g.46591_46595del, NW_016107300.1:g.46592_46595del, NW_016107300.1:g.46593_46595del, NW_016107300.1:g.46594_46595del, NW_016107300.1:g.46595del, NW_016107300.1:g.46595dup, NW_016107300.1:g.46594_46595dup, NW_016107300.1:g.46593_46595dup, NW_016107300.1:g.46592_46595dup, NW_016107300.1:g.46591_46595dup, NW_016107300.1:g.46590_46595dup, NW_016107300.1:g.46589_46595dup, NW_016107300.1:g.46588_46595dup, NW_016107300.1:g.46587_46595dup, NW_016107300.1:g.46586_46595dup, NW_016107300.1:g.46585_46595dup, NW_016107307.1:g.46523_46527delinsTTTTT, NW_016107307.1:g.46523_46539del, NW_016107307.1:g.46523_46538del, NW_016107307.1:g.46523_46537del, NW_016107307.1:g.46523_46536del, NW_016107307.1:g.46523_46535del, NW_016107307.1:g.46523_46534del, NW_016107307.1:g.46523_46533del, NW_016107307.1:g.46523_46532del, NW_016107307.1:g.46523_46531del, NW_016107307.1:g.46523_46530del, NW_016107307.1:g.46523_46529del, NW_016107307.1:g.46489AT[17], NW_016107307.1:g.46523_46527del, NW_016107307.1:g.46523_46527delinsT, NW_016107307.1:g.46523_46527delinsTT, NW_016107307.1:g.46523_46527delinsTTT, NW_016107307.1:g.46523_46527delinsTTTT, NW_016107307.1:g.46523_46527delinsTTTTTT, NW_016107307.1:g.46523_46527delinsTTTTTTT, NW_016107307.1:g.46523_46527delinsTTTTTTTT, NW_016107307.1:g.46523_46527delinsTTTTTTTTT, NW_016107307.1:g.46523_46527delinsTTTTTTTTTT, NW_016107307.1:g.46523_46527delinsTTTTTTTTTTT, NW_016107307.1:g.46523_46527delinsTTTTTTTTTTTT, NW_016107307.1:g.46523_46527delinsTTTTTTTTTTTTT, NW_016107307.1:g.46523_46527delinsTTTTTTTTTTTTTT, NW_016107307.1:g.46523_46527delinsTTTTTTTTTTTTTTT, NW_016107307.1:g.46523_46527delinsTTTTTTTTTTTTTTTT, NT_187643.1:g.124141_124142dup, NT_187643.1:g.124128_124142del, NT_187643.1:g.124129_124142del, NT_187643.1:g.124130_124142del, NT_187643.1:g.124131_124142del, NT_187643.1:g.124132_124142del, NT_187643.1:g.124133_124142del, NT_187643.1:g.124134_124142del, NT_187643.1:g.124135_124142del, NT_187643.1:g.124136_124142del, NT_187643.1:g.124137_124142del, NT_187643.1:g.124138_124142del, NT_187643.1:g.124139_124142del, NT_187643.1:g.124140_124142del, NT_187643.1:g.124141_124142del, NT_187643.1:g.124142del, NT_187643.1:g.124142dup, NT_187643.1:g.124140_124142dup, NT_187643.1:g.124139_124142dup, NT_187643.1:g.124138_124142dup, NT_187643.1:g.124137_124142dup, NT_187643.1:g.124136_124142dup, NT_187643.1:g.124135_124142dup, NT_187643.1:g.124134_124142dup, NT_187643.1:g.124133_124142dup, NT_187643.1:g.124132_124142dup, NT_187643.1:g.124131_124142dup, NT_187643.1:g.124130_124142dup, NT_187676.1:g.20890_20891dup, NT_187676.1:g.20877_20891del, NT_187676.1:g.20878_20891del, NT_187676.1:g.20879_20891del, NT_187676.1:g.20880_20891del, NT_187676.1:g.20881_20891del, NT_187676.1:g.20882_20891del, NT_187676.1:g.20883_20891del, NT_187676.1:g.20884_20891del, NT_187676.1:g.20885_20891del, NT_187676.1:g.20886_20891del, NT_187676.1:g.20887_20891del, NT_187676.1:g.20888_20891del, NT_187676.1:g.20889_20891del, NT_187676.1:g.20890_20891del, NT_187676.1:g.20891del, NT_187676.1:g.20891dup, NT_187676.1:g.20889_20891dup, NT_187676.1:g.20888_20891dup, NT_187676.1:g.20887_20891dup, NT_187676.1:g.20886_20891dup, NT_187676.1:g.20885_20891dup, NT_187676.1:g.20884_20891dup, NT_187676.1:g.20883_20891dup, NT_187676.1:g.20882_20891dup, NT_187676.1:g.20881_20891dup, NT_187676.1:g.20880_20891dup, NT_187676.1:g.20879_20891dup, NT_187641.1:g.163467_163468dup, NT_187641.1:g.163454_163468del, NT_187641.1:g.163455_163468del, NT_187641.1:g.163456_163468del, NT_187641.1:g.163457_163468del, NT_187641.1:g.163458_163468del, NT_187641.1:g.163459_163468del, NT_187641.1:g.163460_163468del, NT_187641.1:g.163461_163468del, NT_187641.1:g.163462_163468del, NT_187641.1:g.163463_163468del, NT_187641.1:g.163464_163468del, NT_187641.1:g.163465_163468del, NT_187641.1:g.163466_163468del, NT_187641.1:g.163467_163468del, NT_187641.1:g.163468del, NT_187641.1:g.163468dup, NT_187641.1:g.163466_163468dup, NT_187641.1:g.163465_163468dup, NT_187641.1:g.163464_163468dup, NT_187641.1:g.163463_163468dup, NT_187641.1:g.163462_163468dup, NT_187641.1:g.163461_163468dup, NT_187641.1:g.163460_163468dup, NT_187641.1:g.163459_163468dup, NT_187641.1:g.163458_163468dup, NT_187641.1:g.163457_163468dup, NT_187641.1:g.163456_163468dup, NT_187645.1:g.124162dup, NT_187645.1:g.124147_124162del, NT_187645.1:g.124148_124162del, NT_187645.1:g.124149_124162del, NT_187645.1:g.124150_124162del, NT_187645.1:g.124151_124162del, NT_187645.1:g.124152_124162del, NT_187645.1:g.124153_124162del, NT_187645.1:g.124154_124162del, NT_187645.1:g.124155_124162del, NT_187645.1:g.124156_124162del, NT_187645.1:g.124157_124162del, NT_187645.1:g.124158_124162del, NT_187645.1:g.124159_124162del, NT_187645.1:g.124160_124162del, NT_187645.1:g.124161_124162del, NT_187645.1:g.124162del, NT_187645.1:g.124161_124162dup, NT_187645.1:g.124160_124162dup, NT_187645.1:g.124159_124162dup, NT_187645.1:g.124158_124162dup, NT_187645.1:g.124157_124162dup, NT_187645.1:g.124156_124162dup, NT_187645.1:g.124155_124162dup, NT_187645.1:g.124154_124162dup, NT_187645.1:g.124153_124162dup, NT_187645.1:g.124152_124162dup, NT_187645.1:g.124151_124162dup, NT_187685.1:g.123627_123631dup, NT_187685.1:g.123620_123631del, NT_187685.1:g.123621_123631del, NT_187685.1:g.123622_123631del, NT_187685.1:g.123623_123631del, NT_187685.1:g.123624_123631del, NT_187685.1:g.123625_123631del, NT_187685.1:g.123626_123631del, NT_187685.1:g.123627_123631del, NT_187685.1:g.123628_123631del, NT_187685.1:g.123629_123631del, NT_187685.1:g.123630_123631del, NT_187685.1:g.123631del, NT_187685.1:g.123631dup, NT_187685.1:g.123630_123631dup, NT_187685.1:g.123629_123631dup, NT_187685.1:g.123628_123631dup, NT_187685.1:g.123626_123631dup, NT_187685.1:g.123625_123631dup, NT_187685.1:g.123624_123631dup, NT_187685.1:g.123623_123631dup, NT_187685.1:g.123622_123631dup, NT_187685.1:g.123621_123631dup, NT_187685.1:g.123620_123631dup, NT_187685.1:g.123619_123631dup, NT_187685.1:g.123618_123631dup, NT_187685.1:g.123617_123631dup, NT_187685.1:g.123616_123631dup, NT_187669.1:g.124134_124139dup, NT_187669.1:g.124129_124139del, NT_187669.1:g.124130_124139del, NT_187669.1:g.124131_124139del, NT_187669.1:g.124132_124139del, NT_187669.1:g.124133_124139del, NT_187669.1:g.124134_124139del, NT_187669.1:g.124135_124139del, NT_187669.1:g.124136_124139del, NT_187669.1:g.124137_124139del, NT_187669.1:g.124138_124139del, NT_187669.1:g.124139del, NT_187669.1:g.124139dup, NT_187669.1:g.124138_124139dup, NT_187669.1:g.124137_124139dup, NT_187669.1:g.124136_124139dup, NT_187669.1:g.124135_124139dup, NT_187669.1:g.124133_124139dup, NT_187669.1:g.124132_124139dup, NT_187669.1:g.124131_124139dup, NT_187669.1:g.124130_124139dup, NT_187669.1:g.124129_124139dup, NT_187669.1:g.124128_124139dup, NT_187669.1:g.124127_124139dup, NT_187669.1:g.124126_124139dup, NT_187669.1:g.124125_124139dup, NT_187669.1:g.124124_124139dup, NT_187669.1:g.124123_124139dup, NW_016107311.1:g.46553delinsTTTTTTTT, NW_016107311.1:g.46553_46562del, NW_016107311.1:g.46553_46561del, NW_016107311.1:g.46553_46560del, NW_016107311.1:g.46553_46559del, NW_016107311.1:g.46553_46558del, NW_016107311.1:g.46553_46557del, NW_016107311.1:g.46553_46556del, NW_016107311.1:g.46553_46555del, NW_016107311.1:g.46519AT[17], NW_016107311.1:g.46553del, NW_016107311.1:g.46553A>T, NW_016107311.1:g.46553delinsTT, NW_016107311.1:g.46553delinsTTT, NW_016107311.1:g.46553delinsTTTT, NW_016107311.1:g.46553delinsTTTTT, NW_016107311.1:g.46553delinsTTTTTT, NW_016107311.1:g.46553delinsTTTTTTT, NW_016107311.1:g.46553delinsTTTTTTTTT, NW_016107311.1:g.46553delinsTTTTTTTTTT, NW_016107311.1:g.46553delinsTTTTTTTTTTT, NW_016107311.1:g.46553delinsTTTTTTTTTTTT, NW_016107311.1:g.46553delinsTTTTTTTTTTTTT, NW_016107311.1:g.46553delinsTTTTTTTTTTTTTT, NW_016107311.1:g.46553delinsTTTTTTTTTTTTTTT, NW_016107311.1:g.46553delinsTTTTTTTTTTTTTTTT, NW_016107311.1:g.46553delinsTTTTTTTTTTTTTTTTT, NW_016107311.1:g.46553delinsTTTTTTTTTTTTTTTTTT, NW_016107311.1:g.46553delinsTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.487182_487192delinsTTTTTTTTTTT, NW_003571061.2:g.487182_487198del, NW_003571061.2:g.487182_487197del, NW_003571061.2:g.487182_487196del, NW_003571061.2:g.487182_487195del, NW_003571061.2:g.487182_487194del, NW_003571061.2:g.487146AT[18], NW_003571061.2:g.487182_487192del, NW_003571061.2:g.487182_487192delinsT, NW_003571061.2:g.487182_487192delinsTT, NW_003571061.2:g.487182_487192delinsTTT, NW_003571061.2:g.487182_487192delinsTTTT, NW_003571061.2:g.487182_487192delinsTTTTT, NW_003571061.2:g.487182_487192delinsTTTTTT, NW_003571061.2:g.487182_487192delinsTTTTTTT, NW_003571061.2:g.487182_487192delinsTTTTTTTT, NW_003571061.2:g.487182_487192delinsTTTTTTTTT, NW_003571061.2:g.487182_487192delinsTTTTTTTTTT, NW_003571061.2:g.487182_487192delinsTTTTTTTTTTTT, NW_003571061.2:g.487182_487192delinsTTTTTTTTTTTTT, NW_003571061.2:g.487182_487192delinsTTTTTTTTTTTTTT, NW_003571061.2:g.487182_487192delinsTTTTTTTTTTTTTTT, NW_003571061.2:g.487182_487192delinsTTTTTTTTTTTTTTTT, NW_003571061.2:g.487182_487192delinsTTTTTTTTTTTTTTTTT, NW_003571061.2:g.487182_487192delinsTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.487182_487192delinsTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.487182_487192delinsTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.487182_487192delinsTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.487182_487192delinsTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.487181_487191delinsTTTTTTTTTTT, NW_003571061.1:g.487181_487197del, NW_003571061.1:g.487181_487196del, NW_003571061.1:g.487181_487195del, NW_003571061.1:g.487181_487194del, NW_003571061.1:g.487181_487193del, NW_003571061.1:g.487145AT[18], NW_003571061.1:g.487181_487191del, NW_003571061.1:g.487181_487191delinsT, NW_003571061.1:g.487181_487191delinsTT, NW_003571061.1:g.487181_487191delinsTTT, NW_003571061.1:g.487181_487191delinsTTTT, NW_003571061.1:g.487181_487191delinsTTTTT, NW_003571061.1:g.487181_487191delinsTTTTTT, NW_003571061.1:g.487181_487191delinsTTTTTTT, NW_003571061.1:g.487181_487191delinsTTTTTTTT, NW_003571061.1:g.487181_487191delinsTTTTTTTTT, NW_003571061.1:g.487181_487191delinsTTTTTTTTTT, NW_003571061.1:g.487181_487191delinsTTTTTTTTTTTT, NW_003571061.1:g.487181_487191delinsTTTTTTTTTTTTT, NW_003571061.1:g.487181_487191delinsTTTTTTTTTTTTTT, NW_003571061.1:g.487181_487191delinsTTTTTTTTTTTTTTT, NW_003571061.1:g.487181_487191delinsTTTTTTTTTTTTTTTT, NW_003571061.1:g.487181_487191delinsTTTTTTTTTTTTTTTTT, NW_003571061.1:g.487181_487191delinsTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.487181_487191delinsTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.487181_487191delinsTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.487181_487191delinsTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.487181_487191delinsTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.743855_743859delinsTTTTT, NW_003571056.2:g.743855_743871del, NW_003571056.2:g.743855_743870del, NW_003571056.2:g.743855_743869del, NW_003571056.2:g.743855_743868del, NW_003571056.2:g.743855_743867del, NW_003571056.2:g.743855_743866del, NW_003571056.2:g.743855_743865del, NW_003571056.2:g.743855_743864del, NW_003571056.2:g.743855_743863del, NW_003571056.2:g.743855_743862del, NW_003571056.2:g.743855_743861del, NW_003571056.2:g.743819AT[18], NW_003571056.2:g.743855_743859del, NW_003571056.2:g.743855_743859delinsT, NW_003571056.2:g.743855_743859delinsTT, NW_003571056.2:g.743855_743859delinsTTT, NW_003571056.2:g.743855_743859delinsTTTT, NW_003571056.2:g.743855_743859delinsTTTTTT, NW_003571056.2:g.743855_743859delinsTTTTTTT, NW_003571056.2:g.743855_743859delinsTTTTTTTT, NW_003571056.2:g.743855_743859delinsTTTTTTTTT, NW_003571056.2:g.743855_743859delinsTTTTTTTTTT, NW_003571056.2:g.743855_743859delinsTTTTTTTTTTT, NW_003571056.2:g.743855_743859delinsTTTTTTTTTTTT, NW_003571056.2:g.743855_743859delinsTTTTTTTTTTTTT, NW_003571056.2:g.743855_743859delinsTTTTTTTTTTTTTT, NW_003571056.2:g.743855_743859delinsTTTTTTTTTTTTTTT, NW_003571056.2:g.743855_743859delinsTTTTTTTTTTTTTTTT, NW_003571056.1:g.743854_743858delinsTTTTT, NW_003571056.1:g.743854_743870del, NW_003571056.1:g.743854_743869del, NW_003571056.1:g.743854_743868del, NW_003571056.1:g.743854_743867del, NW_003571056.1:g.743854_743866del, NW_003571056.1:g.743854_743865del, NW_003571056.1:g.743854_743864del, NW_003571056.1:g.743854_743863del, NW_003571056.1:g.743854_743862del, NW_003571056.1:g.743854_743861del, NW_003571056.1:g.743854_743860del, NW_003571056.1:g.743818AT[18], NW_003571056.1:g.743854_743858del, NW_003571056.1:g.743854_743858delinsT, NW_003571056.1:g.743854_743858delinsTT, NW_003571056.1:g.743854_743858delinsTTT, NW_003571056.1:g.743854_743858delinsTTTT, NW_003571056.1:g.743854_743858delinsTTTTTT, NW_003571056.1:g.743854_743858delinsTTTTTTT, NW_003571056.1:g.743854_743858delinsTTTTTTTT, NW_003571056.1:g.743854_743858delinsTTTTTTTTT, NW_003571056.1:g.743854_743858delinsTTTTTTTTTT, NW_003571056.1:g.743854_743858delinsTTTTTTTTTTT, NW_003571056.1:g.743854_743858delinsTTTTTTTTTTTT, NW_003571056.1:g.743854_743858delinsTTTTTTTTTTTTT, NW_003571056.1:g.743854_743858delinsTTTTTTTTTTTTTT, NW_003571056.1:g.743854_743858delinsTTTTTTTTTTTTTTT, NW_003571056.1:g.743854_743858delinsTTTTTTTTTTTTTTTT, NT_187675.1:g.87969_87970insTTTTTTTTTTTTTTT, NT_187675.1:g.87968_87969del, NT_187675.1:g.87969del, NT_187675.1:g.87969dup, NT_187675.1:g.87968_87969dup, NT_187675.1:g.87967_87969dup, NT_187675.1:g.87966_87969dup, NT_187675.1:g.87965_87969dup, NT_187675.1:g.87964_87969dup, NT_187675.1:g.87963_87969dup, NT_187675.1:g.87962_87969dup, NT_187675.1:g.87969_87970insTTTTTTTTT, NT_187675.1:g.87969_87970insTTTTTTTTTT, NT_187675.1:g.87969_87970insTTTTTTTTTTT, NT_187675.1:g.87969_87970insTTTTTTTTTTTT, NT_187675.1:g.87969_87970insTTTTTTTTTTTTT, NT_187675.1:g.87969_87970insTTTTTTTTTTTTTT, NT_187675.1:g.87969_87970insTTTTTTTTTTTTTTTT, NT_187675.1:g.87969_87970insTTTTTTTTTTTTTTTTT, NT_187675.1:g.87969_87970insTTTTTTTTTTTTTTTTTT, NT_187675.1:g.87969_87970insTTTTTTTTTTTTTTTTTTT, NT_187675.1:g.87969_87970insTTTTTTTTTTTTTTTTTTTT, NT_187675.1:g.87969_87970insTTTTTTTTTTTTTTTTTTTTT, NT_187675.1:g.87969_87970insTTTTTTTTTTTTTTTTTTTTTT, NT_187675.1:g.87969_87970insTTTTTTTTTTTTTTTTTTTTTTT, NT_187675.1:g.87969_87970insTTTTTTTTTTTTTTTTTTTTTTTT, NT_187675.1:g.87969_87970insTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187675.1:g.87969_87970insTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_016107306.1:g.46363_46369dup, NW_016107306.1:g.46360_46369del, NW_016107306.1:g.46361_46369del, NW_016107306.1:g.46362_46369del, NW_016107306.1:g.46363_46369del, NW_016107306.1:g.46364_46369del, NW_016107306.1:g.46365_46369del, NW_016107306.1:g.46366_46369del, NW_016107306.1:g.46367_46369del, NW_016107306.1:g.46368_46369del, NW_016107306.1:g.46369del, NW_016107306.1:g.46369dup, NW_016107306.1:g.46368_46369dup, NW_016107306.1:g.46367_46369dup, NW_016107306.1:g.46366_46369dup, NW_016107306.1:g.46365_46369dup, NW_016107306.1:g.46364_46369dup, NW_016107306.1:g.46362_46369dup, NW_016107306.1:g.46361_46369dup, NW_016107306.1:g.46360_46369dup, NW_016107306.1:g.46359_46369dup, NW_016107306.1:g.46358_46369dup, NW_016107306.1:g.46357_46369dup, NW_016107306.1:g.46356_46369dup, NW_016107306.1:g.46355_46369dup, NW_016107306.1:g.46354_46369dup, NW_016107306.1:g.46369_46370insTTTTTTTTTTTTTTTTT, NW_016107306.1:g.46369_46370insTTTTTTTTTTTTTTTTTT, NT_187636.1:g.157788_157789insAAAAAAAAAAAAAAA, NT_187636.1:g.157787_157788del, NT_187636.1:g.157788del, NT_187636.1:g.157788dup, NT_187636.1:g.157787_157788dup, NT_187636.1:g.157786_157788dup, NT_187636.1:g.157785_157788dup, NT_187636.1:g.157784_157788dup, NT_187636.1:g.157783_157788dup, NT_187636.1:g.157782_157788dup, NT_187636.1:g.157781_157788dup, NT_187636.1:g.157788_157789insAAAAAAAAA, NT_187636.1:g.157788_157789insAAAAAAAAAA, NT_187636.1:g.157788_157789insAAAAAAAAAAA, NT_187636.1:g.157788_157789insAAAAAAAAAAAA, NT_187636.1:g.157788_157789insAAAAAAAAAAAAA, NT_187636.1:g.157788_157789insAAAAAAAAAAAAAA, NT_187636.1:g.157788_157789insAAAAAAAAAAAAAAAA, NT_187636.1:g.157788_157789insAAAAAAAAAAAAAAAAA, NT_187636.1:g.157788_157789insAAAAAAAAAAAAAAAAAA, NT_187636.1:g.157788_157789insAAAAAAAAAAAAAAAAAAA, NT_187636.1:g.157788_157789insAAAAAAAAAAAAAAAAAAAA, NT_187636.1:g.157788_157789insAAAAAAAAAAAAAAAAAAAAA, NT_187636.1:g.157788_157789insAAAAAAAAAAAAAAAAAAAAAA, NT_187636.1:g.157788_157789insAAAAAAAAAAAAAAAAAAAAAAA, NT_187636.1:g.157788_157789insAAAAAAAAAAAAAAAAAAAAAAAA, NT_187636.1:g.157788_157789insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187636.1:g.157788_157789insAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187686.1:g.124486_124487insAAAAAAAAAAAAAAA, NT_187686.1:g.124485_124486del, NT_187686.1:g.124486del, NT_187686.1:g.124486dup, NT_187686.1:g.124485_124486dup, NT_187686.1:g.124484_124486dup, NT_187686.1:g.124483_124486dup, NT_187686.1:g.124482_124486dup, NT_187686.1:g.124481_124486dup, NT_187686.1:g.124480_124486dup, NT_187686.1:g.124479_124486dup, NT_187686.1:g.124486_124487insAAAAAAAAA, NT_187686.1:g.124486_124487insAAAAAAAAAA, NT_187686.1:g.124486_124487insAAAAAAAAAAA, NT_187686.1:g.124486_124487insAAAAAAAAAAAA, NT_187686.1:g.124486_124487insAAAAAAAAAAAAA, NT_187686.1:g.124486_124487insAAAAAAAAAAAAAA, NT_187686.1:g.124486_124487insAAAAAAAAAAAAAAAA, NT_187686.1:g.124486_124487insAAAAAAAAAAAAAAAAA, NT_187686.1:g.124486_124487insAAAAAAAAAAAAAAAAAA, NT_187686.1:g.124486_124487insAAAAAAAAAAAAAAAAAAA, NT_187686.1:g.124486_124487insAAAAAAAAAAAAAAAAAAAA, NT_187686.1:g.124486_124487insAAAAAAAAAAAAAAAAAAAAA, NT_187686.1:g.124486_124487insAAAAAAAAAAAAAAAAAAAAAA, NT_187686.1:g.124486_124487insAAAAAAAAAAAAAAAAAAAAAAA, NT_187686.1:g.124486_124487insAAAAAAAAAAAAAAAAAAAAAAAA, NT_187686.1:g.124486_124487insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187686.1:g.124486_124487insAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187640.1:g.113249_113250insAAAAAAAAAAAAAAA, NT_187640.1:g.113248_113249del, NT_187640.1:g.113249del, NT_187640.1:g.113249dup, NT_187640.1:g.113248_113249dup, NT_187640.1:g.113247_113249dup, NT_187640.1:g.113246_113249dup, NT_187640.1:g.113245_113249dup, NT_187640.1:g.113244_113249dup, NT_187640.1:g.113243_113249dup, NT_187640.1:g.113242_113249dup, NT_187640.1:g.113249_113250insAAAAAAAAA, NT_187640.1:g.113249_113250insAAAAAAAAAA, NT_187640.1:g.113249_113250insAAAAAAAAAAA, NT_187640.1:g.113249_113250insAAAAAAAAAAAA, NT_187640.1:g.113249_113250insAAAAAAAAAAAAA, NT_187640.1:g.113249_113250insAAAAAAAAAAAAAA, NT_187640.1:g.113249_113250insAAAAAAAAAAAAAAAA, NT_187640.1:g.113249_113250insAAAAAAAAAAAAAAAAA, NT_187640.1:g.113249_113250insAAAAAAAAAAAAAAAAAA, NT_187640.1:g.113249_113250insAAAAAAAAAAAAAAAAAAA, NT_187640.1:g.113249_113250insAAAAAAAAAAAAAAAAAAAA, NT_187640.1:g.113249_113250insAAAAAAAAAAAAAAAAAAAAA, NT_187640.1:g.113249_113250insAAAAAAAAAAAAAAAAAAAAAA, NT_187640.1:g.113249_113250insAAAAAAAAAAAAAAAAAAAAAAA, NT_187640.1:g.113249_113250insAAAAAAAAAAAAAAAAAAAAAAAA, NT_187640.1:g.113249_113250insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187640.1:g.113249_113250insAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187638.1:g.94253_94263delinsAAAAAAAAAAA, NT_187638.1:g.94248_94264del, NT_187638.1:g.94249_94264del, NT_187638.1:g.94250_94264del, NT_187638.1:g.94251_94264del, NT_187638.1:g.94252_94264del, NT_187638.1:g.94253TA[20], NT_187638.1:g.94253_94263del, NT_187638.1:g.94253_94263delinsA, NT_187638.1:g.94253_94263delinsAA, NT_187638.1:g.94253_94263delinsAAA, NT_187638.1:g.94253_94263delinsAAAA, NT_187638.1:g.94253_94263delinsAAAAA, NT_187638.1:g.94253_94263delinsAAAAAA, NT_187638.1:g.94253_94263delinsAAAAAAA, NT_187638.1:g.94253_94263delinsAAAAAAAA, NT_187638.1:g.94253_94263delinsAAAAAAAAA, NT_187638.1:g.94253_94263delinsAAAAAAAAAA, NT_187638.1:g.94253_94263delinsAAAAAAAAAAAA, NT_187638.1:g.94253_94263delinsAAAAAAAAAAAAA, NT_187638.1:g.94253_94263delinsAAAAAAAAAAAAAA, NT_187638.1:g.94253_94263delinsAAAAAAAAAAAAAAA, NT_187638.1:g.94253_94263delinsAAAAAAAAAAAAAAAA, NT_187638.1:g.94253_94263delinsAAAAAAAAAAAAAAAAA, NT_187638.1:g.94253_94263delinsAAAAAAAAAAAAAAAAAA, NT_187638.1:g.94253_94263delinsAAAAAAAAAAAAAAAAAAA, NT_187638.1:g.94253_94263delinsAAAAAAAAAAAAAAAAAAAA, NT_187638.1:g.94253_94263delinsAAAAAAAAAAAAAAAAAAAAA, NT_187638.1:g.94253_94263delinsAAAAAAAAAAAAAAAAAAAAAA, NT_187642.1:g.92777_92783delinsAAAAAAA, NT_187642.1:g.92768_92784del, NT_187642.1:g.92769_92784del, NT_187642.1:g.92770_92784del, NT_187642.1:g.92771_92784del, NT_187642.1:g.92772_92784del, NT_187642.1:g.92773_92784del, NT_187642.1:g.92774_92784del, NT_187642.1:g.92775_92784del, NT_187642.1:g.92776_92784del, NT_187642.1:g.92777TA[19], NT_187642.1:g.92777_92783del, NT_187642.1:g.92777_92783delinsA, NT_187642.1:g.92777_92783delinsAA, NT_187642.1:g.92777_92783delinsAAA, NT_187642.1:g.92777_92783delinsAAAA, NT_187642.1:g.92777_92783delinsAAAAA, NT_187642.1:g.92777_92783delinsAAAAAA, NT_187642.1:g.92777_92783delinsAAAAAAAA, NT_187642.1:g.92777_92783delinsAAAAAAAAA, NT_187642.1:g.92777_92783delinsAAAAAAAAAA, NT_187642.1:g.92777_92783delinsAAAAAAAAAAA, NT_187642.1:g.92777_92783delinsAAAAAAAAAAAA, NT_187642.1:g.92777_92783delinsAAAAAAAAAAAAA, NT_187642.1:g.92777_92783delinsAAAAAAAAAAAAAA, NT_187642.1:g.92777_92783delinsAAAAAAAAAAAAAAA, NT_187642.1:g.92777_92783delinsAAAAAAAAAAAAAAAA, NT_187642.1:g.92777_92783delinsAAAAAAAAAAAAAAAAA, NT_187642.1:g.92777_92783delinsAAAAAAAAAAAAAAAAAA, NC_000019.9:g.55256408A>T, NC_000019.9:g.55256408_55256424del, NC_000019.9:g.55256408_55256423del, NC_000019.9:g.55256408_55256422del, NC_000019.9:g.55256408_55256421del, NC_000019.9:g.55256408_55256420del, NC_000019.9:g.55256408_55256419del, NC_000019.9:g.55256408_55256418del, NC_000019.9:g.55256408_55256417del, NC_000019.9:g.55256408_55256416del, NC_000019.9:g.55256408_55256415del, NC_000019.9:g.55256408_55256414del, NC_000019.9:g.55256408_55256413del, NC_000019.9:g.55256408_55256412del, NC_000019.9:g.55256408_55256411del, NC_000019.9:g.55256408_55256410del, NC_000019.9:g.55256370AT[19], NC_000019.9:g.55256408del, NC_000019.9:g.55256408delinsTT, NC_000019.9:g.55256408delinsTTT, NC_000019.9:g.55256408delinsTTTT, NC_000019.9:g.55256408delinsTTTTT, NC_000019.9:g.55256408delinsTTTTTT, NC_000019.9:g.55256408delinsTTTTTTT, NC_000019.9:g.55256408delinsTTTTTTTT, NC_000019.9:g.55256408delinsTTTTTTTTT, NC_000019.9:g.55256408delinsTTTTTTTTTT, NC_000019.9:g.55256408delinsTTTTTTTTTTT, NC_000019.9:g.55256408delinsTTTTTTTTTTTT, NW_003571059.1:g.727811_727812dup, NW_003571059.1:g.727798_727812del, NW_003571059.1:g.727799_727812del, NW_003571059.1:g.727800_727812del, NW_003571059.1:g.727801_727812del, NW_003571059.1:g.727802_727812del, NW_003571059.1:g.727803_727812del, NW_003571059.1:g.727804_727812del, NW_003571059.1:g.727805_727812del, NW_003571059.1:g.727806_727812del, NW_003571059.1:g.727807_727812del, NW_003571059.1:g.727808_727812del, NW_003571059.1:g.727809_727812del, NW_003571059.1:g.727810_727812del, NW_003571059.1:g.727811_727812del, NW_003571059.1:g.727812del, NW_003571059.1:g.727812dup, NW_003571059.1:g.727810_727812dup, NW_003571059.1:g.727809_727812dup, NW_003571059.1:g.727808_727812dup, NW_003571059.1:g.727807_727812dup, NW_003571059.1:g.727806_727812dup, NW_003571059.1:g.727805_727812dup, NW_003571059.1:g.727804_727812dup, NW_003571059.1:g.727803_727812dup, NW_003571059.1:g.727802_727812dup, NW_003571059.1:g.727801_727812dup, NW_003571059.1:g.727800_727812dup

                8.

                rs1491121199 has merged into rs58651549 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  TATATA>-,TA,TATA,TATATATA,TATATATACATTTTTATATATATATATATATATA,TATATATATA,TATATATATATA [Show Flanks]
                  Chromosome:
                  19:54776250 (GRCh38)
                  19:55287702 (GRCh37)
                  Canonical SPDI:
                  NC_000019.10:54776237:TATATATATATATATATA:TATATATATATA,NC_000019.10:54776237:TATATATATATATATATA:TATATATATATATA,NC_000019.10:54776237:TATATATATATATATATA:TATATATATATATATA,NC_000019.10:54776237:TATATATATATATATATA:TATATATATATATATATATA,NC_000019.10:54776237:TATATATATATATATATA:TATATATATATATATATATACATTTTTATATATATATATATATATA,NC_000019.10:54776237:TATATATATATATATATA:TATATATATATATATATATATA,NC_000019.10:54776237:TATATATATATATATATA:TATATATATATATATATATATATA
                  Gene:
                  KIR2DL1 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  TATATATATATATATA=0./0 (ALFA)
                  TA=0.02113/352 (TOMMO)
                  TA=0.05263/2 (GENOME_DK)
                  TA=0.25/2 (KOREAN)
                  HGVS:
                  NC_000019.10:g.54776238TA[6], NC_000019.10:g.54776238TA[7], NC_000019.10:g.54776238TA[8], NC_000019.10:g.54776238TA[10], NC_000019.10:g.54776238_54776255TA[10]CATTTTTATATATATATATATATATA[1], NC_000019.10:g.54776238TA[11], NC_000019.10:g.54776238TA[12], NW_004166865.1:g.750606TA[6], NW_004166865.1:g.750606TA[7], NW_004166865.1:g.750606TA[8], NW_004166865.1:g.750606TA[10], NW_004166865.1:g.750606_750623TA[10]CATTTTTATATATATATATATATATA[1], NW_004166865.1:g.750606TA[11], NW_004166865.1:g.750606TA[12], NG_051369.1:g.12031TA[6], NG_051369.1:g.12031TA[7], NG_051369.1:g.12031TA[8], NG_051369.1:g.12031TA[10], NG_051369.1:g.12031_12048TA[10]CATTTTTATATATATATATATATATA[1], NG_051369.1:g.12031TA[11], NG_051369.1:g.12031TA[12], NW_016107309.1:g.77845TA[6], NW_016107309.1:g.77845TA[7], NW_016107309.1:g.77845TA[8], NW_016107309.1:g.77845TA[10], NW_016107309.1:g.77845_77862TA[10]CATTTTTATATATATATATATATATA[1], NW_016107309.1:g.77845TA[11], NW_016107309.1:g.77845TA[12], NW_016107307.1:g.77805TA[6], NW_016107307.1:g.77805TA[7], NW_016107307.1:g.77805TA[8], NW_016107307.1:g.77805TA[10], NW_016107307.1:g.77805_77822TA[10]CATTTTTATATATATATATATATATA[1], NW_016107307.1:g.77805TA[11], NW_016107307.1:g.77805TA[12], NW_016107304.1:g.77848TA[6], NW_016107304.1:g.77848TA[7], NW_016107304.1:g.77848TA[8], NW_016107304.1:g.77848TA[10], NW_016107304.1:g.77848_77865TA[10]CATTTTTATATATATATATATATATA[1], NW_016107304.1:g.77848TA[11], NW_016107304.1:g.77848TA[12], NW_016107303.1:g.77816TA[6], NW_016107303.1:g.77816TA[7], NW_016107303.1:g.77816TA[8], NW_016107303.1:g.77816TA[10], NW_016107303.1:g.77816_77833TA[10]CATTTTTATATATATATATATATATA[1], NW_016107303.1:g.77816TA[11], NW_016107303.1:g.77816TA[12], NW_016107300.1:g.77871TA[6], NW_016107300.1:g.77871TA[7], NW_016107300.1:g.77871TA[8], NW_016107300.1:g.77871TA[10], NW_016107300.1:g.77871_77888TA[10]CATTTTTATATATATATATATATATA[1], NW_016107300.1:g.77871TA[11], NW_016107300.1:g.77871TA[12], NW_003571060.1:g.680572TA[6], NW_003571060.1:g.680572TA[7], NW_003571060.1:g.680572TA[8], NW_003571060.1:g.680572TA[10], NW_003571060.1:g.680572_680589TA[10]CATTTTTATATATATATATATATATA[1], NW_003571060.1:g.680572TA[11], NW_003571060.1:g.680572TA[12], NT_187693.1:g.758804TA[6], NT_187693.1:g.758804TA[7], NT_187693.1:g.758804TA[8], NT_187693.1:g.758804TA[10], NT_187693.1:g.758804_758821TA[10]CATTTTTATATATATATATATATATA[1], NT_187693.1:g.758804TA[11], NT_187693.1:g.758804TA[12], NC_000019.9:g.55287690TA[6], NC_000019.9:g.55287690TA[7], NC_000019.9:g.55287690TA[8], NC_000019.9:g.55287690TA[10], NC_000019.9:g.55287690_55287707TA[10]CATTTTTATATATATATATATATATA[1], NC_000019.9:g.55287690TA[11], NC_000019.9:g.55287690TA[12], NT_187685.1:g.92336TA[6], NT_187685.1:g.92336TA[7], NT_187685.1:g.92336TA[8], NT_187685.1:g.92336TA[10], NT_187685.1:g.92336_92353TA[10]A[4]TGTATATATATATATATATATA[1], NT_187685.1:g.92336TA[11], NT_187685.1:g.92336TA[12], NT_187676.1:g.52152TA[6], NT_187676.1:g.52152TA[7], NT_187676.1:g.52152TA[8], NT_187676.1:g.52152TA[10], NT_187676.1:g.52152_52169TA[10]CATTTTTATATATATATATATATATA[1], NT_187676.1:g.52152TA[11], NT_187676.1:g.52152TA[12], NT_187673.1:g.92823TA[6], NT_187673.1:g.92823TA[7], NT_187673.1:g.92823TA[8], NT_187673.1:g.92823TA[10], NT_187673.1:g.92823_92840TA[10]A[4]TGTATATATATATATATATATA[1], NT_187673.1:g.92823TA[11], NT_187673.1:g.92823TA[12], NT_187672.1:g.77816TA[6], NT_187672.1:g.77816TA[7], NT_187672.1:g.77816TA[8], NT_187672.1:g.77816TA[10], NT_187672.1:g.77816_77833TA[10]CATTTTTATATATATATATATATATA[1], NT_187672.1:g.77816TA[11], NT_187672.1:g.77816TA[12], NT_187669.1:g.92844TA[6], NT_187669.1:g.92844TA[7], NT_187669.1:g.92844TA[8], NT_187669.1:g.92844TA[10], NT_187669.1:g.92844_92861TA[10]A[4]TGTATATATATATATATATATA[1], NT_187669.1:g.92844TA[11], NT_187669.1:g.92844TA[12], NT_187645.1:g.92860TA[6], NT_187645.1:g.92860TA[7], NT_187645.1:g.92860TA[8], NT_187645.1:g.92860TA[10], NT_187645.1:g.92860_92877TA[10]A[4]TGTATATATATATATATATATA[1], NT_187645.1:g.92860TA[11], NT_187645.1:g.92860TA[12], NT_187643.1:g.92844TA[6], NT_187643.1:g.92844TA[7], NT_187643.1:g.92844TA[8], NT_187643.1:g.92844TA[10], NT_187643.1:g.92844_92861TA[10]A[4]TGTATATATATATATATATATA[1], NT_187643.1:g.92844TA[11], NT_187643.1:g.92844TA[12], NT_187641.1:g.132170TA[6], NT_187641.1:g.132170TA[7], NT_187641.1:g.132170TA[8], NT_187641.1:g.132170TA[10], NT_187641.1:g.132170_132187TA[10]A[4]TGTATATATATATATATATATA[1], NT_187641.1:g.132170TA[11], NT_187641.1:g.132170TA[12], NT_187639.1:g.93153TA[6], NT_187639.1:g.93153TA[7], NT_187639.1:g.93153TA[8], NT_187639.1:g.93153TA[10], NT_187639.1:g.93153_93170TA[10]A[4]TGTATATATATATATATATATA[1], NT_187639.1:g.93153TA[11], NT_187639.1:g.93153TA[12], NT_187637.1:g.92584TA[6], NT_187637.1:g.92584TA[7], NT_187637.1:g.92584TA[8], NT_187637.1:g.92584TA[10], NT_187637.1:g.92584_92601TA[10]A[4]TGTATATATATATATATATATA[1], NT_187637.1:g.92584TA[11], NT_187637.1:g.92584TA[12], NT_187671.1:g.55151TA[6], NT_187671.1:g.55151TA[7], NT_187671.1:g.55151TA[8], NT_187671.1:g.55151TA[10], NT_187671.1:g.55151_55168TA[10]CATTTTTATATATATATATATATATA[1], NT_187671.1:g.55151TA[11], NT_187671.1:g.55151TA[12], NW_016107305.1:g.77832TA[6], NW_016107305.1:g.77832TA[7], NW_016107305.1:g.77832TA[8], NW_016107305.1:g.77832TA[10], NW_016107305.1:g.77832_77849TA[10]CATTTTTATATATATATATATATATA[1], NW_016107305.1:g.77832TA[11], NW_016107305.1:g.77832TA[12], NW_016107301.1:g.77876TA[6], NW_016107301.1:g.77876TA[7], NW_016107301.1:g.77876TA[8], NW_016107301.1:g.77876TA[10], NW_016107301.1:g.77876_77893TA[10]CATTTTTATATATATATATATATATA[1], NW_016107301.1:g.77876TA[11], NW_016107301.1:g.77876TA[12], NW_003571054.1:g.681896TA[6], NW_003571054.1:g.681896TA[7], NW_003571054.1:g.681896TA[8], NW_003571054.1:g.681896TA[10], NW_003571054.1:g.681896_681913TA[10]CATTTTTATATATATATATATATATA[1], NW_003571054.1:g.681896TA[11], NW_003571054.1:g.681896TA[12], NT_187687.1:g.92648TA[6], NT_187687.1:g.92648TA[7], NT_187687.1:g.92648TA[8], NT_187687.1:g.92648TA[10], NT_187687.1:g.92648_92665TA[10]A[4]TGTATATATATATATATATATA[1], NT_187687.1:g.92648TA[11], NT_187687.1:g.92648TA[12], NT_187683.1:g.50414TA[6], NT_187683.1:g.50414TA[7], NT_187683.1:g.50414TA[8], NT_187683.1:g.50414TA[10], NT_187683.1:g.50414_50431TA[10]CATTTTTATATATATATATATATATA[1], NT_187683.1:g.50414TA[11], NT_187683.1:g.50414TA[12], NT_187674.1:g.63075TA[6], NT_187674.1:g.63075TA[7], NT_187674.1:g.63075TA[8], NT_187674.1:g.63075TA[10], NT_187674.1:g.63075_63092TA[10]CATTTTTATATATATATATATATATA[1], NT_187674.1:g.63075TA[11], NT_187674.1:g.63075TA[12], NW_016107306.1:g.77654C>T, NW_016107306.1:g.77654_77659del, NW_016107306.1:g.77654_77657del, NW_016107306.1:g.77654_77655del, NW_016107306.1:g.77654delinsTAT, NW_016107306.1:g.77654delinsTATATATATATATATACATTTTTATATAT, NW_016107306.1:g.77654delinsTATAT, NW_016107306.1:g.77654delinsTATATAT, NW_016107302.1:g.77845TA[6], NW_016107302.1:g.77845TA[7], NW_016107302.1:g.77845TA[8], NW_016107302.1:g.77845TA[10], NW_016107302.1:g.77845_77862TA[10]CATTTTTATATATATATATATATATA[1], NW_016107302.1:g.77845TA[11], NW_016107302.1:g.77845TA[12], NT_187686.1:g.93206G>A, NT_187686.1:g.93206_93211del, NT_187686.1:g.93206_93209del, NT_187686.1:g.93206_93207del, NT_187686.1:g.93206delinsATA, NT_187686.1:g.93206delinsATATATAAAAATGTATATATATATATATA, NT_187686.1:g.93206delinsATATA, NT_187686.1:g.93206delinsATATATA, NT_187675.1:g.119240C>T, NT_187675.1:g.119240_119245del, NT_187675.1:g.119240_119243del, NT_187675.1:g.119240_119241del, NT_187675.1:g.119240delinsTAT, NT_187675.1:g.119240delinsTATATATATATATATACATTTTTATATAT, NT_187675.1:g.119240delinsTATAT, NT_187675.1:g.119240delinsTATATAT, NT_187668.1:g.82745TA[6], NT_187668.1:g.82745TA[7], NT_187668.1:g.82745TA[8], NT_187668.1:g.82745TA[10], NT_187668.1:g.82745_82762TA[10]A[4]TGTATATATATATATATATATA[1], NT_187668.1:g.82745TA[11], NT_187668.1:g.82745TA[12], NT_187640.1:g.81970G>A, NT_187640.1:g.81970_81975del, NT_187640.1:g.81970_81973del, NT_187640.1:g.81970_81971del, NT_187640.1:g.81970delinsATA, NT_187640.1:g.81970delinsATATATAAAAATGTATATATATATATATA, NT_187640.1:g.81970delinsATATA, NT_187640.1:g.81970delinsATATATA, NT_187636.1:g.126510G>A, NT_187636.1:g.126510_126515del, NT_187636.1:g.126510_126513del, NT_187636.1:g.126510_126511del, NT_187636.1:g.126510delinsATA, NT_187636.1:g.126510delinsATATATAAAAATGTATATATATATATATA, NT_187636.1:g.126510delinsATATA, NT_187636.1:g.126510delinsATATATA, NT_113949.2:g.114627_114629delinsTAT, NT_113949.2:g.114627_114632del, NT_113949.2:g.114627_114630del, NT_113949.2:g.114627_114629delinsT, NT_113949.2:g.114627_114629delinsTATAT, NT_113949.2:g.114627_114629delinsTATATATATATATATATATAAAAATGTATAT, NT_113949.2:g.114627_114629delinsTATATAT, NT_113949.2:g.114627_114629delinsTATATATAT, NT_113949.1:g.28361_28363delinsATA, NT_113949.1:g.28359_28364del, NT_113949.1:g.28370_28373del, NT_113949.1:g.28361_28363delinsA, NT_113949.1:g.28361_28363delinsATATA, NT_113949.1:g.28361_28363delinsATATACATTTTTATATATATATATATATATA, NT_113949.1:g.28361_28363delinsATATATA, NT_113949.1:g.28361_28363delinsATATATATA, NW_016107313.1:g.77863TA[6], NW_016107313.1:g.77863TA[7], NW_016107313.1:g.77863TA[8], NW_016107313.1:g.77863TA[10], NW_016107313.1:g.77863_77880TA[10]CATTTTTATATATATATATATATATA[1], NW_016107313.1:g.77863TA[11], NW_016107313.1:g.77863TA[12], NT_187670.1:g.121795TA[14], NT_187670.1:g.121795TA[15], NT_187670.1:g.121795TA[16], NT_187670.1:g.121795TA[18], NT_187670.1:g.121795_121816TA[11]A[4]TGTATATATATATATATATATATA[1], NT_187670.1:g.121795TA[19], NT_187670.1:g.121795TA[20], NT_187644.1:g.121703TA[16], NT_187644.1:g.121703TA[17], NT_187644.1:g.121703TA[18], NT_187644.1:g.121703TA[20], NT_187644.1:g.121703_121724TA[11]A[4]TGTATATATATATATATATATATA[1], NT_187644.1:g.121703TA[21], NT_187644.1:g.121703TA[22], NW_016107310.1:g.108223C>T, NW_016107310.1:g.108223_108228del, NW_016107310.1:g.108223_108226del, NW_016107310.1:g.108223_108224del, NW_016107310.1:g.108223delinsTAT, NW_016107310.1:g.108223delinsTATATATATATATATACATTTTTATATAT, NW_016107310.1:g.108223delinsTATAT, NW_016107310.1:g.108223delinsTATATAT, NW_016107311.1:g.77837TA[6], NW_016107311.1:g.77837TA[7], NW_016107311.1:g.77837TA[8], NW_016107311.1:g.77837TA[10], NW_016107311.1:g.77837_77854TA[10]CATTTTTATATATATATATATATATA[1], NW_016107311.1:g.77837TA[11], NW_016107311.1:g.77837TA[12]

                  9.

                  rs1491087170 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    AG>- [Show Flanks]
                    Chromosome:
                    19:54739546 (GRCh38)
                    19:55250992 (GRCh37)
                    Canonical SPDI:
                    NC_000019.10:54739544:GAG:G
                    Gene:
                    KIR2DL3 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    G=0./0 (ALFA)
                    -=0.000007/1 (GnomAD)
                    HGVS:
                    NC_000019.10:g.54739546_54739547del, NW_004166865.1:g.713913_713914del, NG_046935.1:g.6038_6039del, NW_003571059.2:g.722384_722385del, NW_003571059.1:g.722383_722384del, NW_016107308.1:g.41133_41134del, NT_187673.1:g.129532_129533del, NW_016107313.1:g.41166_41167del, NW_016107305.1:g.41134_41135del, NT_187687.1:g.129363_129364del, NT_187674.1:g.26351_26352del, NW_016107302.1:g.41140_41141del, NW_003571054.1:g.645191_645192del, NT_187683.1:g.13721_13722del, NW_016107301.1:g.41167_41168del, NT_187639.1:g.129854_129855del, NW_016107309.1:g.41149_41150del, NW_016107300.1:g.41157_41158del, NW_016107307.1:g.41113_41114del, NW_016107303.1:g.41115_41116del, NT_187693.1:g.722106_722107del, NC_000019.9:g.55250992_55250993del, NT_187672.1:g.41113_41114del, NT_187671.1:g.18449_18450del, NW_016107304.1:g.41148_41149del, NT_187643.1:g.129551_129552del, NT_187676.1:g.15462_15463del, NT_187641.1:g.168877_168878del, NT_187637.1:g.129293_129294del, NW_003571060.1:g.643876_643877del, NT_187645.1:g.129569_129570del, NT_187685.1:g.129038_129039del, NT_187669.1:g.129546_129547del, NW_016107311.1:g.41151_41152del, NT_187684.1:g.159589_159590del, NW_003571061.2:g.481750_481751del, NW_003571061.1:g.481749_481750del, NW_003571056.2:g.738423_738424del, NW_003571056.1:g.738422_738423del, NT_113949.2:g.136365_136366del, NT_187675.1:g.54246_54247del, NW_016107306.1:g.41013_41014del, NT_187636.1:g.191501_191502del, NT_187677.1:g.46691_46692del, NT_187686.1:g.158377_158378del, NT_187668.1:g.147880_147881del, NT_187640.1:g.146928_146929del, NT_187638.1:g.99697_99698del, NT_187670.1:g.143521_143522del, NT_187644.1:g.143433_143434del, NT_187642.1:g.98217_98218del

                    10.

                    rs1490913914 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      A>G [Show Flanks]
                      Chromosome:
                      19:54777643 (GRCh38)
                      19:55289095 (GRCh37)
                      Canonical SPDI:
                      NC_000019.10:54777642:A:G
                      Gene:
                      KIR2DL1 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      G=0./0 (ALFA)
                      G=0.000044/6 (GnomAD)
                      HGVS:
                      NC_000019.10:g.54777643A>G, NW_004166865.1:g.752011A>G, NG_051369.1:g.13436A>G, NW_003571059.2:g.760473A>G, NW_003571059.1:g.760472A>G, NW_003571057.2:g.849750A>G, NW_003571057.1:g.849749A>G, NW_016107309.1:g.79250A>G, NW_016107307.1:g.79211A>G, NW_016107304.1:g.79253A>G, NW_016107303.1:g.79221A>G, NW_016107300.1:g.79276A>G, NW_003571060.1:g.681977A>G, NT_187693.1:g.760209A>G, NC_000019.9:g.55289095A>G, NT_187685.1:g.90948T>C, NT_187676.1:g.53557A>G, NT_187673.1:g.91435T>C, NT_187672.1:g.79221A>G, NT_187669.1:g.91456T>C, NT_187645.1:g.91472T>C, NT_187643.1:g.91456T>C, NT_187641.1:g.130782T>C, NT_187639.1:g.91765T>C, NT_187637.1:g.91196T>C, NT_187671.1:g.56555A>G, NW_016107305.1:g.79238A>G, NW_016107301.1:g.79283A>G, NW_003571054.1:g.683302A>G, NT_187687.1:g.91260T>C, NT_187683.1:g.51819A>G, NT_187674.1:g.64481A>G, NW_016107306.1:g.79054A>G, NW_016107302.1:g.79251A>G, NT_187686.1:g.91806T>C, NT_187684.1:g.92950T>C, NT_187675.1:g.120640A>G, NT_187668.1:g.81358T>C, NT_187640.1:g.80570T>C, NT_187636.1:g.125110T>C, NT_113949.2:g.113229T>C, NT_113949.1:g.29761A>G, NW_016107313.1:g.79280A>G, NT_187670.1:g.120392T>C, NT_187644.1:g.120300T>C, NW_016107310.1:g.109623A>G, NW_016107311.1:g.79241A>G, NW_016107308.1:g.79225A>G

                      11.

                      rs1490761665 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>T [Show Flanks]
                        Chromosome:
                        19:54752945 (GRCh38)
                        19:55264397 (GRCh37)
                        Canonical SPDI:
                        NC_000019.10:54752944:C:T
                        Gene:
                        KIR2DL3 (Varview)
                        Functional Consequence:
                        3_prime_UTR_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        T=0./0 (ALFA)
                        T=0.000015/2 (GnomAD)
                        HGVS:
                        NC_000019.10:g.54752945C>T, NW_004166865.1:g.727312C>T, NG_046935.1:g.19437C>T, NM_015868.3:c.*426C>T, NM_015868.2:c.*426C>T, NW_003571059.2:g.735781C>T, NW_003571059.1:g.735780C>T, NW_016107308.1:g.54533C>T, NT_187673.1:g.116133G>A, NW_016107313.1:g.54574C>T, NW_016107305.1:g.54541C>T, NT_187687.1:g.115956G>A, NT_187674.1:g.39784C>T, NW_016107302.1:g.54554C>T, NW_003571054.1:g.658605C>T, NT_187683.1:g.27122C>T, NW_016107301.1:g.54586C>T, NT_187639.1:g.116463G>A, NW_016107309.1:g.54552C>T, NW_016107300.1:g.54563C>T, NW_016107307.1:g.54512C>T, NW_016107303.1:g.54523C>T, NT_187693.1:g.735511C>T, NC_000019.9:g.55264397C>T, NT_187672.1:g.54522C>T, NT_187671.1:g.31858C>T, NW_016107304.1:g.54553C>T, NT_187643.1:g.116154G>A, NT_187676.1:g.28859C>T, NT_187641.1:g.155480G>A, NT_187637.1:g.115894G>A, NW_003571060.1:g.657279C>T, NT_187645.1:g.116171G>A, NT_187685.1:g.115646G>A, NT_187669.1:g.116154G>A, NW_016107311.1:g.54535C>T, NT_187684.1:g.146187G>A, NW_003571061.2:g.495170C>T, NW_003571061.1:g.495169C>T, NW_003571056.2:g.751843C>T, NW_003571056.1:g.751842C>T, NT_187675.1:g.95923C>T, NW_016107306.1:g.54336C>T, NT_187636.1:g.149827G>A, NT_187677.1:g.60108C>T, NT_187686.1:g.116524G>A, NT_187668.1:g.106071G>A, NT_187640.1:g.105288G>A, NT_187638.1:g.86275G>A, NT_187642.1:g.84795G>A, NM_014511.3:c.*426C>T, NM_014219.2:c.*402C>T, NM_014219.1:c.*402C>T, NM_014513.2:c.*537C>T, NM_014511.1:c.*426C>T

                        12.

                        rs1490617426 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          T>C [Show Flanks]
                          Chromosome:
                          19:54748690 (GRCh38)
                          19:55260142 (GRCh37)
                          Canonical SPDI:
                          NC_000019.10:54748689:T:C
                          Gene:
                          KIR2DL3 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa
                          MAF:
                          C=0./0 (ALFA)
                          C=0.000008/2 (TOPMED)
                          HGVS:
                          NC_000019.10:g.54748690T>C, NW_004166865.1:g.723057T>C, NG_046935.1:g.15182T>C, NW_003571059.2:g.731526T>C, NW_003571059.1:g.731525T>C, NW_016107308.1:g.50278T>C, NT_187673.1:g.120388A>G, NW_016107313.1:g.50319T>C, NW_016107305.1:g.50286T>C, NT_187687.1:g.120211A>G, NT_187674.1:g.35529T>C, NW_016107302.1:g.50299T>C, NW_003571054.1:g.654350T>C, NT_187683.1:g.22867T>C, NW_016107301.1:g.50331T>C, NT_187639.1:g.120718A>G, NW_016107309.1:g.50297T>C, NW_016107300.1:g.50308T>C, NW_016107307.1:g.50257T>C, NW_016107303.1:g.50268T>C, NT_187693.1:g.731256T>C, NC_000019.9:g.55260142T>C, NT_187672.1:g.50267T>C, NT_187671.1:g.27603T>C, NW_016107304.1:g.50298T>C, NT_187643.1:g.120409A>G, NT_187676.1:g.24604T>C, NT_187641.1:g.159735A>G, NT_187637.1:g.120149A>G, NW_003571060.1:g.653024T>C, NT_187645.1:g.120427A>G, NT_187685.1:g.119901A>G, NT_187669.1:g.120409A>G, NW_016107311.1:g.50280T>C, NT_187684.1:g.150443A>G, NW_003571061.2:g.490916T>C, NW_003571061.1:g.490915T>C, NW_003571056.2:g.747589T>C, NW_003571056.1:g.747588T>C, NT_187675.1:g.91669T>C, NW_016107306.1:g.50082T>C, NT_187636.1:g.154081A>G, NT_187677.1:g.55854T>C, NT_187686.1:g.120779A>G, NT_187668.1:g.110323A>G, NT_187640.1:g.109542A>G, NT_187638.1:g.90529A>G, NT_187642.1:g.89049A>G

                          13.

                          rs1490600277 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>C [Show Flanks]
                            Chromosome:
                            19:54742353 (GRCh38)
                            19:55253799 (GRCh37)
                            Canonical SPDI:
                            NC_000019.10:54742352:G:C
                            Gene:
                            KIR2DL3 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            C=0./0 (ALFA)
                            C=0.000011/3 (TOPMED)
                            C=0.000021/3 (GnomAD)
                            HGVS:
                            NC_000019.10:g.54742353G>C, NW_004166865.1:g.716720G>C, NG_046935.1:g.8845G>C, NW_003571059.2:g.725191G>C, NW_003571059.1:g.725190G>C, NW_016107308.1:g.43940G>C, NT_187673.1:g.126725C>G, NW_016107313.1:g.43973G>C, NW_016107305.1:g.43941G>C, NT_187687.1:g.126556C>G, NT_187674.1:g.29158G>C, NW_016107302.1:g.43947G>C, NW_003571054.1:g.647998G>C, NT_187683.1:g.16528G>C, NW_016107301.1:g.43974G>C, NT_187639.1:g.127047C>G, NW_016107309.1:g.43956G>C, NW_016107300.1:g.43969G>C, NW_016107307.1:g.43920G>C, NW_016107303.1:g.43922G>C, NT_187693.1:g.724913G>C, NC_000019.9:g.55253799G>C, NT_187672.1:g.43920G>C, NT_187671.1:g.21256G>C, NW_016107304.1:g.43955G>C, NT_187643.1:g.126744C>G, NT_187676.1:g.18269G>C, NT_187641.1:g.166070C>G, NT_187637.1:g.126486C>G, NW_003571060.1:g.646683G>C, NT_187645.1:g.126762C>G, NT_187685.1:g.126231C>G, NT_187669.1:g.126739C>G, NW_016107311.1:g.43957G>C, NT_187684.1:g.156783C>G, NW_003571061.2:g.484556G>C, NW_003571061.1:g.484555G>C, NW_003571056.2:g.741229G>C, NW_003571056.1:g.741228G>C, NT_113949.2:g.133559C>G, NT_187675.1:g.57052G>C, NW_016107306.1:g.43819G>C, NT_187636.1:g.188695C>G, NT_187677.1:g.49497G>C, NT_187686.1:g.155571C>G, NT_187668.1:g.145074C>G, NT_187640.1:g.144122C>G, NT_187638.1:g.96891C>G, NT_187670.1:g.140715C>G, NT_187644.1:g.140627C>G, NT_187642.1:g.95411C>G

                            14.

                            rs1490502796 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>C,T [Show Flanks]
                              Chromosome:
                              19:54738865 (GRCh38)
                              19:-1 (GRCh37)
                              Canonical SPDI:
                              NC_000019.10:54738864:G:C,NC_000019.10:54738864:G:T
                              Gene:
                              KIR2DL3 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              T=0./0 (ALFA)
                              T=0.0002/12 (GnomAD)
                              HGVS:
                              NC_000019.10:g.54738865G>C, NC_000019.10:g.54738865G>T, NW_004166865.1:g.713232G>C, NW_004166865.1:g.713232G>T, NG_046935.1:g.5357G>C, NG_046935.1:g.5357G>T, NW_003571059.2:g.721703G>C, NW_003571059.2:g.721703G>T, NW_003571059.1:g.721702G>C, NW_003571059.1:g.721702G>T, NW_016107308.1:g.40452G>C, NW_016107308.1:g.40452G>T, NT_187673.1:g.130213C>G, NT_187673.1:g.130213C>A, NW_016107313.1:g.40485G>C, NW_016107313.1:g.40485G>T, NW_016107305.1:g.40453G>C, NW_016107305.1:g.40453G>T, NT_187687.1:g.130044C>G, NT_187687.1:g.130044C>A, NT_187674.1:g.25670G>C, NT_187674.1:g.25670G>T, NW_016107302.1:g.40459G>C, NW_016107302.1:g.40459G>T, NW_003571054.1:g.644510G>C, NW_003571054.1:g.644510G>T, NT_187683.1:g.13040G>C, NT_187683.1:g.13040G>T, NW_016107301.1:g.40486G>C, NW_016107301.1:g.40486G>T, NT_187639.1:g.130535C>G, NT_187639.1:g.130535C>A, NT_187643.1:g.130213C>G, NT_187643.1:g.130213C>A, NT_187641.1:g.169539C>G, NT_187641.1:g.169539C>A, NT_187637.1:g.129955C>G, NT_187637.1:g.129955C>A, NT_187645.1:g.130231C>G, NT_187645.1:g.130231C>A, NT_187685.1:g.129700C>G, NT_187685.1:g.129700C>A, NT_187669.1:g.130208C>G, NT_187669.1:g.130208C>A, NW_016107311.1:g.40470G>C, NW_016107311.1:g.40470G>T, NT_187684.1:g.160270C>G, NT_187684.1:g.160270C>A, NW_003571061.2:g.464887G>C, NW_003571061.2:g.464887G>T, NW_003571061.1:g.464886G>C, NW_003571061.1:g.464886G>T, NW_003571056.2:g.737742G>C, NW_003571056.2:g.737742G>T, NW_003571056.1:g.737741G>C, NW_003571056.1:g.737741G>T, NT_113949.2:g.136930C>G, NT_113949.2:g.136930C>A, NT_187675.1:g.37384G>C, NT_187675.1:g.37384G>T, NW_016107306.1:g.40448G>C, NW_016107306.1:g.40448G>T, NT_187636.1:g.208363C>G, NT_187636.1:g.208363C>A, NT_187677.1:g.29827G>C, NT_187677.1:g.29827G>T, NT_187686.1:g.175239C>G, NT_187686.1:g.175239C>A, NT_187668.1:g.164742C>G, NT_187668.1:g.164742C>A, NT_187640.1:g.163790C>G, NT_187640.1:g.163790C>A, NT_187638.1:g.116559C>G, NT_187638.1:g.116559C>A, NT_187670.1:g.144086C>G, NT_187670.1:g.144086C>A, NT_187644.1:g.143998C>G, NT_187644.1:g.143998C>A, NT_187642.1:g.115080C>G, NT_187642.1:g.115080C>A

                              15.

                              rs1490423675 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                ATATTT>- [Show Flanks]
                                Chromosome:
                                19:54744952 (GRCh38)
                                19:55256409 (GRCh37)
                                Canonical SPDI:
                                NC_000019.10:54744950:TATATTT:T
                                Gene:
                                KIR2DL3 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                T=0.00051/6 (ALFA)
                                ATATATATAT=0.98696/15596 (TOMMO)
                                HGVS:
                                NC_000019.10:g.54744952_54744957del, NW_004166865.1:g.719319_719324del, NG_046935.1:g.11444_11449del, NW_003571059.2:g.727812_727813dup, NW_003571059.2:g.727760AT[15], NW_016107308.1:g.46543A>T, NW_016107308.1:g.46509AT[16], NT_187673.1:g.124122_124127del, NT_187687.1:g.123945_123950del, NW_016107301.1:g.46585_46590del, NW_016107309.1:g.46559_46564del, NW_016107300.1:g.46570_46575del, NW_016107307.1:g.46523A>T, NW_016107307.1:g.46489AT[17], NT_187672.1:g.46527A>T, NT_187672.1:g.46493AT[19], NT_187671.1:g.23863A>T, NT_187671.1:g.23829AT[19], NW_016107304.1:g.46558A>T, NW_016107304.1:g.46524AT[19], NT_187643.1:g.124141_124146del, NT_187676.1:g.20890_20891dup, NT_187676.1:g.20838AT[15], NT_187641.1:g.163467_163472del, NT_187645.1:g.124162AT[17], NT_187645.1:g.124161_124164del, NT_187685.1:g.123630_123635del, NT_187669.1:g.124139_124140insAATA, NT_187669.1:g.124139AT[15], NW_016107311.1:g.46552_46553insTTT, NW_016107311.1:g.46549_46551del, NW_003571061.2:g.487182A>T, NW_003571061.2:g.487146AT[21], NW_003571061.1:g.487181A>T, NW_003571061.1:g.487145AT[21], NW_003571056.2:g.743855A>T, NW_003571056.2:g.743819AT[18], NW_003571056.1:g.743854A>T, NW_003571056.1:g.743818AT[18], NT_187675.1:g.87960_87961delinsTATTT, NT_187675.1:g.87959_87961del, NT_187636.1:g.157789_157790delinsAAATA, NT_187636.1:g.157789_157791del, NT_187686.1:g.124487_124488delinsAAATA, NT_187686.1:g.124487_124489del, NT_187668.1:g.142446T>A, NT_187668.1:g.142442TA[19], NT_187640.1:g.113250_113251delinsAAATA, NT_187640.1:g.113250_113252del, NT_187638.1:g.94263T>A, NT_187638.1:g.94253TA[23], NT_187642.1:g.92783T>A, NT_187642.1:g.92777TA[20], NC_000019.9:g.55256408A>T, NC_000019.9:g.55256370AT[17], NW_003571059.1:g.727811_727812dup, NW_003571059.1:g.727759AT[15]

                                16.

                                rs1490421842 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>A [Show Flanks]
                                  Chromosome:
                                  19:54777859 (GRCh38)
                                  19:55289311 (GRCh37)
                                  Canonical SPDI:
                                  NC_000019.10:54777858:G:A
                                  Gene:
                                  KIR2DL1 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  A=0./0 (ALFA)
                                  HGVS:
                                  NC_000019.10:g.54777859G>A, NW_004166865.1:g.752227G>A, NG_051369.1:g.13652G>A, NW_003571059.2:g.760689G>A, NW_003571059.1:g.760688G>A, NW_003571057.2:g.849966G>A, NW_003571057.1:g.849965G>A, NW_016107309.1:g.79466G>A, NW_016107307.1:g.79427G>A, NW_016107304.1:g.79469G>A, NW_016107303.1:g.79437G>A, NW_016107300.1:g.79492G>A, NW_003571060.1:g.682193G>A, NT_187693.1:g.760425G>A, NC_000019.9:g.55289311G>A, NT_187685.1:g.90732C>T, NT_187676.1:g.53773G>A, NT_187673.1:g.91219C>T, NT_187672.1:g.79437G>A, NT_187669.1:g.91240C>T, NT_187645.1:g.91256C>T, NT_187643.1:g.91240C>T, NT_187641.1:g.130566C>T, NT_187639.1:g.91549C>T, NT_187637.1:g.90980C>T, NT_187671.1:g.56771G>A, NW_016107305.1:g.79454G>A, NW_016107301.1:g.79499G>A, NW_003571054.1:g.683518G>A, NT_187687.1:g.91044C>T, NT_187683.1:g.52035G>A, NT_187674.1:g.64697G>A, NW_016107306.1:g.79270G>A, NW_016107302.1:g.79467G>A, NT_187686.1:g.91590C>T, NT_187684.1:g.92734C>T, NT_187675.1:g.120856G>A, NT_187668.1:g.81142C>T, NT_187640.1:g.80354C>T, NT_187636.1:g.124894C>T, NT_113949.2:g.113013C>T, NT_113949.1:g.29977G>A, NW_016107313.1:g.79496G>A, NT_187670.1:g.120176C>T, NT_187644.1:g.120084C>T, NW_016107310.1:g.109839G>A, NW_016107311.1:g.79457G>A, NW_016107308.1:g.79441G>A

                                  17.

                                  rs1490397683 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    T>A [Show Flanks]
                                    Chromosome:
                                    19:54745270 (GRCh38)
                                    19:55256722 (GRCh37)
                                    Canonical SPDI:
                                    NC_000019.10:54745269:T:A
                                    Gene:
                                    KIR2DL3 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    A=0./0 (ALFA)
                                    A=0.000014/2 (GnomAD)
                                    A=0.000019/5 (TOPMED)
                                    A=0.000625/4 (1000Genomes)
                                    HGVS:
                                    NC_000019.10:g.54745270T>A, NW_004166865.1:g.719637T>A, NG_046935.1:g.11762T>A, NW_003571059.2:g.728106T>A, NW_003571059.1:g.728105T>A, NW_016107308.1:g.46858T>A, NT_187673.1:g.123808A>T, NW_016107313.1:g.46899T>A, NW_016107305.1:g.46866T>A, NT_187687.1:g.123631A>T, NT_187674.1:g.32109T>A, NW_016107302.1:g.46879T>A, NW_003571054.1:g.650930T>A, NT_187683.1:g.19447T>A, NW_016107301.1:g.46911T>A, NT_187639.1:g.124138A>T, NW_016107309.1:g.46877T>A, NW_016107300.1:g.46888T>A, NW_016107307.1:g.46837T>A, NW_016107303.1:g.46848T>A, NT_187693.1:g.727836T>A, NC_000019.9:g.55256722T>A, NT_187672.1:g.46847T>A, NT_187671.1:g.24183T>A, NW_016107304.1:g.46878T>A, NT_187643.1:g.123829A>T, NT_187676.1:g.21184T>A, NT_187641.1:g.163155A>T, NT_187637.1:g.123569A>T, NW_003571060.1:g.649604T>A, NT_187645.1:g.123847A>T, NT_187685.1:g.123321A>T, NT_187669.1:g.123829A>T, NW_016107311.1:g.46860T>A, NT_187684.1:g.153864A>T, NW_003571061.2:g.487496T>A, NW_003571061.1:g.487495T>A, NW_003571056.2:g.744169T>A, NW_003571056.1:g.744168T>A, NT_187675.1:g.88263T>A, NW_016107306.1:g.46662T>A, NT_187636.1:g.157487A>T, NT_187677.1:g.52434T>A, NT_187686.1:g.124185A>T, NT_187668.1:g.113729A>T, NT_187640.1:g.112948A>T, NT_187638.1:g.93949A>T, NT_187642.1:g.92469A>T

                                    18.

                                    rs1490369427 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      A>G,T [Show Flanks]
                                      Chromosome:
                                      19:54739144 (GRCh38)
                                      19:55250590 (GRCh37)
                                      Canonical SPDI:
                                      NC_000019.10:54739143:A:G,NC_000019.10:54739143:A:T
                                      Gene:
                                      KIR2DL3 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      T=0./0 (ALFA)
                                      T=0.00002/2 (GnomAD)
                                      T=0.01745/51 (KOREAN)
                                      HGVS:
                                      NC_000019.10:g.54739144A>G, NC_000019.10:g.54739144A>T, NW_004166865.1:g.713511A>G, NW_004166865.1:g.713511A>T, NG_046935.1:g.5636A>G, NG_046935.1:g.5636A>T, NW_003571059.2:g.721982A>G, NW_003571059.2:g.721982A>T, NW_003571059.1:g.721981A>G, NW_003571059.1:g.721981A>T, NW_016107308.1:g.40731A>G, NW_016107308.1:g.40731A>T, NT_187673.1:g.129934T>C, NT_187673.1:g.129934T>A, NW_016107313.1:g.40764A>G, NW_016107313.1:g.40764A>T, NW_016107305.1:g.40732A>G, NW_016107305.1:g.40732A>T, NT_187687.1:g.129765T>C, NT_187687.1:g.129765T>A, NT_187674.1:g.25949A>G, NT_187674.1:g.25949A>T, NW_016107302.1:g.40738A>G, NW_016107302.1:g.40738A>T, NW_003571054.1:g.644789A>G, NW_003571054.1:g.644789A>T, NT_187683.1:g.13319A>G, NT_187683.1:g.13319A>T, NW_016107301.1:g.40765A>G, NW_016107301.1:g.40765A>T, NT_187639.1:g.130256T>C, NT_187639.1:g.130256T>A, NW_016107309.1:g.40747A>G, NW_016107309.1:g.40747A>T, NW_016107300.1:g.40755A>G, NW_016107300.1:g.40755A>T, NW_016107307.1:g.40711A>G, NW_016107307.1:g.40711A>T, NW_016107303.1:g.40713A>G, NW_016107303.1:g.40713A>T, NT_187693.1:g.721704A>G, NT_187693.1:g.721704A>T, NC_000019.9:g.55250590A>G, NC_000019.9:g.55250590A>T, NT_187672.1:g.40711A>G, NT_187672.1:g.40711A>T, NT_187671.1:g.18047A>G, NT_187671.1:g.18047A>T, NW_016107304.1:g.40746A>G, NW_016107304.1:g.40746A>T, NT_187643.1:g.129953T>C, NT_187643.1:g.129953T>A, NT_187676.1:g.15060A>G, NT_187676.1:g.15060A>T, NT_187641.1:g.169279T>C, NT_187641.1:g.169279T>A, NT_187637.1:g.129695T>C, NT_187637.1:g.129695T>A, NW_003571060.1:g.643474A>G, NW_003571060.1:g.643474A>T, NT_187645.1:g.129971T>C, NT_187645.1:g.129971T>A, NT_187685.1:g.129440T>C, NT_187685.1:g.129440T>A, NT_187669.1:g.129948T>C, NT_187669.1:g.129948T>A, NW_016107311.1:g.40749A>G, NW_016107311.1:g.40749A>T, NT_187684.1:g.159991T>C, NT_187684.1:g.159991T>A, NW_003571061.2:g.465164T>A, NW_003571061.2:g.465164T>G, NW_003571061.1:g.465163T>A, NW_003571061.1:g.465163T>G, NW_003571056.2:g.738021A>G, NW_003571056.2:g.738021A>T, NW_003571056.1:g.738020A>G, NW_003571056.1:g.738020A>T, NT_113949.2:g.136653A>T, NT_113949.2:g.136653A>C, NT_187675.1:g.37661T>A, NT_187675.1:g.37661T>G, NW_016107306.1:g.40649A>G, NW_016107306.1:g.40649A>T, NT_187636.1:g.208086A>T, NT_187636.1:g.208086A>C, NT_187677.1:g.30104T>A, NT_187677.1:g.30104T>G, NT_187686.1:g.174962A>T, NT_187686.1:g.174962A>C, NT_187668.1:g.164465A>T, NT_187668.1:g.164465A>C, NT_187640.1:g.163513A>T, NT_187640.1:g.163513A>C, NT_187638.1:g.116282A>T, NT_187638.1:g.116282A>C, NT_187670.1:g.143809A>T, NT_187670.1:g.143809A>C, NT_187644.1:g.143721A>T, NT_187644.1:g.143721A>C, NT_187642.1:g.114803A>T, NT_187642.1:g.114803A>C

                                      19.

                                      rs1490350292 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>A,G,T [Show Flanks]
                                        Chromosome:
                                        19:54778278 (GRCh38)
                                        19:55289730 (GRCh37)
                                        Canonical SPDI:
                                        NC_000019.10:54778277:C:A,NC_000019.10:54778277:C:G,NC_000019.10:54778277:C:T
                                        Gene:
                                        KIR2DL1 (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        G=0./0 (ALFA)
                                        HGVS:
                                        NC_000019.10:g.54778278C>A, NC_000019.10:g.54778278C>G, NC_000019.10:g.54778278C>T, NW_004166865.1:g.752646C>A, NW_004166865.1:g.752646C>G, NW_004166865.1:g.752646C>T, NG_051369.1:g.14071C>A, NG_051369.1:g.14071C>G, NG_051369.1:g.14071C>T, NW_003571059.2:g.761108C>A, NW_003571059.2:g.761108C>G, NW_003571059.2:g.761108C>T, NW_003571059.1:g.761107C>A, NW_003571059.1:g.761107C>G, NW_003571059.1:g.761107C>T, NW_003571057.2:g.850385C>A, NW_003571057.2:g.850385C>G, NW_003571057.2:g.850385C>T, NW_003571057.1:g.850384C>A, NW_003571057.1:g.850384C>G, NW_003571057.1:g.850384C>T, NW_016107309.1:g.79885C>A, NW_016107309.1:g.79885C>G, NW_016107309.1:g.79885C>T, NW_016107307.1:g.79846C>A, NW_016107307.1:g.79846C>G, NW_016107307.1:g.79846C>T, NW_016107304.1:g.79888C>A, NW_016107304.1:g.79888C>G, NW_016107304.1:g.79888C>T, NW_016107303.1:g.79856C>A, NW_016107303.1:g.79856C>G, NW_016107303.1:g.79856C>T, NW_016107300.1:g.79911C>A, NW_016107300.1:g.79911C>G, NW_016107300.1:g.79911C>T, NW_003571060.1:g.682612C>A, NW_003571060.1:g.682612C>G, NW_003571060.1:g.682612C>T, NT_187693.1:g.760844C>A, NT_187693.1:g.760844C>G, NT_187693.1:g.760844C>T, NC_000019.9:g.55289730C>A, NC_000019.9:g.55289730C>G, NC_000019.9:g.55289730C>T, NT_187685.1:g.90313G>T, NT_187685.1:g.90313G>C, NT_187685.1:g.90313G>A, NT_187676.1:g.54192C>A, NT_187676.1:g.54192C>G, NT_187676.1:g.54192C>T, NT_187673.1:g.90800G>T, NT_187673.1:g.90800G>C, NT_187673.1:g.90800G>A, NT_187672.1:g.79856C>A, NT_187672.1:g.79856C>G, NT_187672.1:g.79856C>T, NT_187669.1:g.90821G>T, NT_187669.1:g.90821G>C, NT_187669.1:g.90821G>A, NT_187645.1:g.90837G>T, NT_187645.1:g.90837G>C, NT_187645.1:g.90837G>A, NT_187643.1:g.90821G>T, NT_187643.1:g.90821G>C, NT_187643.1:g.90821G>A, NT_187641.1:g.130147G>T, NT_187641.1:g.130147G>C, NT_187641.1:g.130147G>A, NT_187639.1:g.91130G>T, NT_187639.1:g.91130G>C, NT_187639.1:g.91130G>A, NT_187637.1:g.90561G>T, NT_187637.1:g.90561G>C, NT_187637.1:g.90561G>A, NT_187671.1:g.57190C>A, NT_187671.1:g.57190C>G, NT_187671.1:g.57190C>T, NW_016107305.1:g.79873C>A, NW_016107305.1:g.79873C>G, NW_016107305.1:g.79873C>T, NW_016107301.1:g.79918C>A, NW_016107301.1:g.79918C>G, NW_016107301.1:g.79918C>T, NW_003571054.1:g.683937C>A, NW_003571054.1:g.683937C>G, NW_003571054.1:g.683937C>T, NT_187687.1:g.90625G>T, NT_187687.1:g.90625G>C, NT_187687.1:g.90625G>A, NT_187683.1:g.52454C>A, NT_187683.1:g.52454C>G, NT_187683.1:g.52454C>T, NT_187674.1:g.65116C>A, NT_187674.1:g.65116C>G, NT_187674.1:g.65116C>T, NW_016107306.1:g.79689C>A, NW_016107306.1:g.79689C>G, NW_016107306.1:g.79689C>T, NW_016107302.1:g.79886C>A, NW_016107302.1:g.79886C>G, NW_016107302.1:g.79886C>T, NT_187686.1:g.91171G>T, NT_187686.1:g.91171G>C, NT_187686.1:g.91171G>A, NT_187684.1:g.92315G>T, NT_187684.1:g.92315G>C, NT_187684.1:g.92315G>A, NT_187675.1:g.121275C>A, NT_187675.1:g.121275C>G, NT_187675.1:g.121275C>T, NT_187668.1:g.80723G>T, NT_187668.1:g.80723G>C, NT_187668.1:g.80723G>A, NT_187640.1:g.79935G>T, NT_187640.1:g.79935G>C, NT_187640.1:g.79935G>A, NT_187636.1:g.124475G>T, NT_187636.1:g.124475G>C, NT_187636.1:g.124475G>A, NT_113949.2:g.112593G>T, NT_113949.2:g.112593G>C, NT_113949.2:g.112593G>A, NT_113949.1:g.30397C>A, NT_113949.1:g.30397C>G, NT_113949.1:g.30397C>T, NW_016107313.1:g.79915C>A, NW_016107313.1:g.79915C>G, NW_016107313.1:g.79915C>T, NT_187670.1:g.119756G>T, NT_187670.1:g.119756G>C, NT_187670.1:g.119756G>A, NT_187644.1:g.119664G>T, NT_187644.1:g.119664G>C, NT_187644.1:g.119664G>A, NW_016107310.1:g.110258C>A, NW_016107310.1:g.110258C>G, NW_016107310.1:g.110258C>T, NW_016107311.1:g.79876C>A, NW_016107311.1:g.79876C>G, NW_016107311.1:g.79876C>T, NW_016107308.1:g.79860C>A, NW_016107308.1:g.79860C>G, NW_016107308.1:g.79860C>T

                                        20.

                                        rs1490131590 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          19:54751560 (GRCh38)
                                          19:55263012 (GRCh37)
                                          Canonical SPDI:
                                          NC_000019.10:54751559:G:A
                                          Gene:
                                          KIR2DL3 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          A=0.000071/1 (ALFA)
                                          A=0.000004/1 (TOPMED)
                                          A=0.000008/1 (GnomAD)
                                          HGVS:
                                          NC_000019.10:g.54751560G>A, NW_004166865.1:g.725927G>A, NG_046935.1:g.18052G>A, NW_003571059.2:g.734396G>A, NW_003571059.1:g.734395G>A, NW_016107308.1:g.53148G>A, NT_187673.1:g.117518C>T, NW_016107313.1:g.53189G>A, NW_016107305.1:g.53156G>A, NT_187687.1:g.117341C>T, NT_187674.1:g.38399G>A, NW_016107302.1:g.53169G>A, NW_003571054.1:g.657220G>A, NT_187683.1:g.25737G>A, NW_016107301.1:g.53201G>A, NT_187639.1:g.117848C>T, NW_016107309.1:g.53167G>A, NW_016107300.1:g.53178G>A, NW_016107307.1:g.53127G>A, NW_016107303.1:g.53138G>A, NT_187693.1:g.734126G>A, NC_000019.9:g.55263012G>A, NT_187672.1:g.53137G>A, NT_187671.1:g.30473G>A, NW_016107304.1:g.53168G>A, NT_187643.1:g.117539C>T, NT_187676.1:g.27474G>A, NT_187641.1:g.156865C>T, NT_187637.1:g.117279C>T, NW_003571060.1:g.655894G>A, NT_187645.1:g.117556C>T, NT_187685.1:g.117031C>T, NT_187669.1:g.117539C>T, NW_016107311.1:g.53150G>A, NT_187684.1:g.147572C>T, NW_003571061.2:g.493788G>A, NW_003571061.1:g.493787G>A, NW_003571056.2:g.750461G>A, NW_003571056.1:g.750460G>A, NT_187675.1:g.94538G>A, NW_016107306.1:g.52951G>A, NT_187636.1:g.151212C>T, NT_187677.1:g.58726G>A, NT_187686.1:g.117909C>T, NT_187668.1:g.107456C>T, NT_187640.1:g.106673C>T, NT_187638.1:g.87657C>T, NT_187642.1:g.86177C>T

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