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1.

rs1491575152 has merged into rs200199853 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    TT>-,T,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT [Show Flanks]
    Chromosome:
    19:54761532 (GRCh38)
    19:55272984 (GRCh37)
    Canonical SPDI:
    NC_000019.10:54761524:TTTTTTTTT:TTTTTTT,NC_000019.10:54761524:TTTTTTTTT:TTTTTTTT,NC_000019.10:54761524:TTTTTTTTT:TTTTTTTTTT,NC_000019.10:54761524:TTTTTTTTT:TTTTTTTTTTT,NC_000019.10:54761524:TTTTTTTTT:TTTTTTTTTTTT,NC_000019.10:54761524:TTTTTTTTT:TTTTTTTTTTTTTT,NC_000019.10:54761524:TTTTTTTTT:TTTTTTTTTTTTTTT
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    TTTTTTTT=0./0 (ALFA)
    -=0.01757/88 (1000Genomes)
    -=0.12714/490 (ALSPAC)
    -=0.13781/511 (TWINSUK)
    HGVS:
    NC_000019.10:g.54761532_54761533del, NC_000019.10:g.54761533del, NC_000019.10:g.54761533dup, NC_000019.10:g.54761532_54761533dup, NC_000019.10:g.54761531_54761533dup, NC_000019.10:g.54761529_54761533dup, NC_000019.10:g.54761528_54761533dup, NW_004166865.1:g.735899_735900del, NW_004166865.1:g.735900del, NW_004166865.1:g.735900dup, NW_004166865.1:g.735899_735900dup, NW_004166865.1:g.735898_735900dup, NW_004166865.1:g.735896_735900dup, NW_004166865.1:g.735895_735900dup, NG_033793.2:g.6877_6878del, NG_033793.2:g.6878del, NG_033793.2:g.6878dup, NG_033793.2:g.6877_6878dup, NG_033793.2:g.6876_6878dup, NG_033793.2:g.6874_6878dup, NG_033793.2:g.6873_6878dup, NW_003571059.2:g.744368_744369del, NW_003571059.2:g.744369del, NW_003571059.2:g.744369dup, NW_003571059.2:g.744368_744369dup, NW_003571059.2:g.744367_744369dup, NW_003571059.2:g.744365_744369dup, NW_003571059.2:g.744364_744369dup, NW_003571059.1:g.744367_744368del, NW_003571059.1:g.744368del, NW_003571059.1:g.744368dup, NW_003571059.1:g.744367_744368dup, NW_003571059.1:g.744366_744368dup, NW_003571059.1:g.744364_744368dup, NW_003571059.1:g.744363_744368dup, NW_016107309.1:g.63139_63140del, NW_016107309.1:g.63140del, NW_016107309.1:g.63140dup, NW_016107309.1:g.63139_63140dup, NW_016107309.1:g.63138_63140dup, NW_016107309.1:g.63136_63140dup, NW_016107309.1:g.63135_63140dup, NW_016107308.1:g.63120_63121del, NW_016107308.1:g.63121del, NW_016107308.1:g.63121dup, NW_016107308.1:g.63120_63121dup, NW_016107308.1:g.63119_63121dup, NW_016107308.1:g.63117_63121dup, NW_016107308.1:g.63116_63121dup, NW_016107307.1:g.63099_63100del, NW_016107307.1:g.63100del, NW_016107307.1:g.63100dup, NW_016107307.1:g.63099_63100dup, NW_016107307.1:g.63098_63100dup, NW_016107307.1:g.63096_63100dup, NW_016107307.1:g.63095_63100dup, NW_016107304.1:g.63142_63143del, NW_016107304.1:g.63143del, NW_016107304.1:g.63143dup, NW_016107304.1:g.63142_63143dup, NW_016107304.1:g.63141_63143dup, NW_016107304.1:g.63139_63143dup, NW_016107304.1:g.63138_63143dup, NW_016107303.1:g.63110_63111del, NW_016107303.1:g.63111del, NW_016107303.1:g.63111dup, NW_016107303.1:g.63110_63111dup, NW_016107303.1:g.63109_63111dup, NW_016107303.1:g.63107_63111dup, NW_016107303.1:g.63106_63111dup, NW_016107300.1:g.63165_63166del, NW_016107300.1:g.63166del, NW_016107300.1:g.63166dup, NW_016107300.1:g.63165_63166dup, NW_016107300.1:g.63164_63166dup, NW_016107300.1:g.63162_63166dup, NW_016107300.1:g.63161_63166dup, NW_003571060.1:g.665866_665867del, NW_003571060.1:g.665867del, NW_003571060.1:g.665867dup, NW_003571060.1:g.665866_665867dup, NW_003571060.1:g.665865_665867dup, NW_003571060.1:g.665863_665867dup, NW_003571060.1:g.665862_665867dup, NT_187693.1:g.744098_744099del, NT_187693.1:g.744099del, NT_187693.1:g.744099dup, NT_187693.1:g.744098_744099dup, NT_187693.1:g.744097_744099dup, NT_187693.1:g.744095_744099dup, NT_187693.1:g.744094_744099dup, NC_000019.9:g.55272984_55272985del, NC_000019.9:g.55272985del, NC_000019.9:g.55272985dup, NC_000019.9:g.55272984_55272985dup, NC_000019.9:g.55272983_55272985dup, NC_000019.9:g.55272981_55272985dup, NC_000019.9:g.55272980_55272985dup, NT_187685.1:g.107065_107066del, NT_187685.1:g.107066del, NT_187685.1:g.107066dup, NT_187685.1:g.107065_107066dup, NT_187685.1:g.107064_107066dup, NT_187685.1:g.107062_107066dup, NT_187685.1:g.107061_107066dup, NT_187676.1:g.37446_37447del, NT_187676.1:g.37447del, NT_187676.1:g.37447dup, NT_187676.1:g.37446_37447dup, NT_187676.1:g.37445_37447dup, NT_187676.1:g.37443_37447dup, NT_187676.1:g.37442_37447dup, NT_187673.1:g.107552_107553del, NT_187673.1:g.107553del, NT_187673.1:g.107553dup, NT_187673.1:g.107552_107553dup, NT_187673.1:g.107551_107553dup, NT_187673.1:g.107549_107553dup, NT_187673.1:g.107548_107553dup, NT_187672.1:g.63110_63111del, NT_187672.1:g.63111del, NT_187672.1:g.63111dup, NT_187672.1:g.63110_63111dup, NT_187672.1:g.63109_63111dup, NT_187672.1:g.63107_63111dup, NT_187672.1:g.63106_63111dup, NT_187671.1:g.40445_40446del, NT_187671.1:g.40446del, NT_187671.1:g.40446dup, NT_187671.1:g.40445_40446dup, NT_187671.1:g.40444_40446dup, NT_187671.1:g.40442_40446dup, NT_187671.1:g.40441_40446dup, NT_187669.1:g.107573_107574del, NT_187669.1:g.107574del, NT_187669.1:g.107574dup, NT_187669.1:g.107573_107574dup, NT_187669.1:g.107572_107574dup, NT_187669.1:g.107570_107574dup, NT_187669.1:g.107569_107574dup, NT_187645.1:g.107589_107590del, NT_187645.1:g.107590del, NT_187645.1:g.107590dup, NT_187645.1:g.107589_107590dup, NT_187645.1:g.107588_107590dup, NT_187645.1:g.107586_107590dup, NT_187645.1:g.107585_107590dup, NT_187643.1:g.107573_107574del, NT_187643.1:g.107574del, NT_187643.1:g.107574dup, NT_187643.1:g.107573_107574dup, NT_187643.1:g.107572_107574dup, NT_187643.1:g.107570_107574dup, NT_187643.1:g.107569_107574dup, NT_187641.1:g.146899_146900del, NT_187641.1:g.146900del, NT_187641.1:g.146900dup, NT_187641.1:g.146899_146900dup, NT_187641.1:g.146898_146900dup, NT_187641.1:g.146896_146900dup, NT_187641.1:g.146895_146900dup, NT_187639.1:g.107882_107883del, NT_187639.1:g.107883del, NT_187639.1:g.107883dup, NT_187639.1:g.107882_107883dup, NT_187639.1:g.107881_107883dup, NT_187639.1:g.107879_107883dup, NT_187639.1:g.107878_107883dup, NT_187637.1:g.107313_107314del, NT_187637.1:g.107314del, NT_187637.1:g.107314dup, NT_187637.1:g.107313_107314dup, NT_187637.1:g.107312_107314dup, NT_187637.1:g.107310_107314dup, NT_187637.1:g.107309_107314dup, NW_016107313.1:g.63159_63160del, NW_016107313.1:g.63160del, NW_016107313.1:g.63160dup, NW_016107313.1:g.63159_63160dup, NW_016107313.1:g.63158_63160dup, NW_016107313.1:g.63156_63160dup, NW_016107313.1:g.63155_63160dup, NW_016107311.1:g.63120_63121del, NW_016107311.1:g.63121del, NW_016107311.1:g.63121dup, NW_016107311.1:g.63120_63121dup, NW_016107311.1:g.63119_63121dup, NW_016107311.1:g.63117_63121dup, NW_016107311.1:g.63116_63121dup, NW_016107305.1:g.63126_63127del, NW_016107305.1:g.63127del, NW_016107305.1:g.63127dup, NW_016107305.1:g.63126_63127dup, NW_016107305.1:g.63125_63127dup, NW_016107305.1:g.63123_63127dup, NW_016107305.1:g.63122_63127dup, NW_016107302.1:g.63139_63140del, NW_016107302.1:g.63140del, NW_016107302.1:g.63140dup, NW_016107302.1:g.63139_63140dup, NW_016107302.1:g.63138_63140dup, NW_016107302.1:g.63136_63140dup, NW_016107302.1:g.63135_63140dup, NW_003571054.1:g.667190_667191del, NW_003571054.1:g.667191del, NW_003571054.1:g.667191dup, NW_003571054.1:g.667190_667191dup, NW_003571054.1:g.667189_667191dup, NW_003571054.1:g.667187_667191dup, NW_003571054.1:g.667186_667191dup, NT_187687.1:g.107377_107378del, NT_187687.1:g.107378del, NT_187687.1:g.107378dup, NT_187687.1:g.107377_107378dup, NT_187687.1:g.107376_107378dup, NT_187687.1:g.107374_107378dup, NT_187687.1:g.107373_107378dup, NT_187674.1:g.48369_48370del, NT_187674.1:g.48370del, NT_187674.1:g.48370dup, NT_187674.1:g.48369_48370dup, NT_187674.1:g.48368_48370dup, NT_187674.1:g.48366_48370dup, NT_187674.1:g.48365_48370dup, NT_187668.1:g.97475_97476del, NT_187668.1:g.97476del, NT_187668.1:g.97476dup, NT_187668.1:g.97475_97476dup, NT_187668.1:g.97474_97476dup, NT_187668.1:g.97472_97476dup, NT_187668.1:g.97471_97476dup, NW_016107310.1:g.93512_93513del, NW_016107310.1:g.93513del, NW_016107310.1:g.93513dup, NW_016107310.1:g.93512_93513dup, NW_016107310.1:g.93511_93513dup, NW_016107310.1:g.93509_93513dup, NW_016107310.1:g.93508_93513dup, NW_016107306.1:g.62942_62943del, NW_016107306.1:g.62943del, NW_016107306.1:g.62943dup, NW_016107306.1:g.62942_62943dup, NW_016107306.1:g.62941_62943dup, NW_016107306.1:g.62939_62943dup, NW_016107306.1:g.62938_62943dup, NW_016107301.1:g.63170_63171del, NW_016107301.1:g.63171del, NW_016107301.1:g.63171dup, NW_016107301.1:g.63170_63171dup, NW_016107301.1:g.63169_63171dup, NW_016107301.1:g.63167_63171dup, NW_016107301.1:g.63166_63171dup, NT_187684.1:g.109068_109069del, NT_187684.1:g.109069del, NT_187684.1:g.109069dup, NT_187684.1:g.109068_109069dup, NT_187684.1:g.109067_109069dup, NT_187684.1:g.109065_109069dup, NT_187684.1:g.109064_109069dup, NT_187683.1:g.35707dup, NT_187683.1:g.35707del, NT_187683.1:g.35706_35707dup, NT_187683.1:g.35705_35707dup, NT_187683.1:g.35704_35707dup, NT_187683.1:g.35702_35707dup, NT_187683.1:g.35701_35707dup, NT_187675.1:g.104529_104530del, NT_187675.1:g.104530del, NT_187675.1:g.104530dup, NT_187675.1:g.104529_104530dup, NT_187675.1:g.104528_104530dup, NT_187675.1:g.104526_104530dup, NT_187675.1:g.104525_104530dup, NW_003571057.2:g.833645_833646del, NW_003571057.2:g.833646del, NW_003571057.2:g.833646dup, NW_003571057.2:g.833645_833646dup, NW_003571057.2:g.833644_833646dup, NW_003571057.2:g.833642_833646dup, NW_003571057.2:g.833641_833646dup, NW_003571057.1:g.833644_833645del, NW_003571057.1:g.833645del, NW_003571057.1:g.833645dup, NW_003571057.1:g.833644_833645dup, NW_003571057.1:g.833643_833645dup, NW_003571057.1:g.833641_833645dup, NW_003571057.1:g.833640_833645dup

    2.

    rs1491565387 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      ->GCATGT,GT [Show Flanks]
      Chromosome:
      19:54903390 (GRCh38)
      19:55414751 (GRCh37)
      Canonical SPDI:
      NC_000019.10:54903390:T:TGCATGT,NC_000019.10:54903390:T:TGT
      Gene:
      NCR1 (Varview)
      Functional Consequence:
      intron_variant,genic_upstream_transcript_variant
      Validated:
      by frequency,by alfa
      MAF:
      TGT=0./0 (ALFA)
      TGCATG=0.000008/1 (GnomAD)
      HGVS:
      NC_000019.10:g.54903391_54903392insGCATGT, NC_000019.10:g.54903391_54903392insGT, NW_004166865.1:g.877759_877760insGCATGT, NW_004166865.1:g.877759_877760insGT, NW_003571061.2:g.615544_615545insGCATGT, NW_003571061.2:g.615544_615545insGT, NW_003571061.1:g.615543_615544insGCATGT, NW_003571061.1:g.615543_615544insGT, NW_003571055.2:g.548573_548574insGCATGT, NW_003571055.2:g.548573_548574insGT, NW_003571055.1:g.548572_548573insGCATGT, NW_003571055.1:g.548572_548573insGT, NW_003571059.2:g.821748_821749insGCATGT, NW_003571059.2:g.821748_821749insGT, NW_003571056.2:g.883369_883370insGCATGT, NW_003571056.2:g.883369_883370insGT, NW_003571057.2:g.910906_910907insGCATGT, NW_003571057.2:g.910906_910907insGT, NW_003571058.2:g.885455_885456insGCATGT, NW_003571058.2:g.885455_885456insGT, NT_187693.1:g.885865_885866insGCATGT, NT_187693.1:g.885865_885866insGT, NC_000019.9:g.55414751_55414752insGCATGT, NC_000019.9:g.55414751_55414752insGT, NW_003571060.1:g.807751_807752insGCATGT, NW_003571060.1:g.807751_807752insGT, NW_003571054.1:g.806781_806782insGCATGT, NW_003571054.1:g.806781_806782insGT, NT_187675.1:g.273630_273631insGCATGT, NT_187675.1:g.273630_273631insGT, NT_187674.1:g.189411_189412insGCATGT, NT_187674.1:g.189411_189412insGT, NT_187671.1:g.182338_182339insGCATGT, NT_187671.1:g.182338_182339insGT, NT_187676.1:g.179341_179342insGCATGT, NT_187676.1:g.179341_179342insGT, NT_187683.1:g.177609_177610insGCATGT, NT_187683.1:g.177609_177610insGT, NW_016107304.1:g.232464_232465insGCATGT, NW_016107304.1:g.232464_232465insGT, NT_187677.1:g.180758_180759insGCATGT, NT_187677.1:g.180758_180759insGT, NW_016107312.1:g.8595_8596insCATGCA, NW_016107312.1:g.8595_8596insCA

      3.

      rs1491561202 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        ->CGCA,CTCA [Show Flanks]
        Chromosome:
        19:54903358 (GRCh38)
        19:55414719 (GRCh37)
        Canonical SPDI:
        NC_000019.10:54903358:CA:CACGCA,NC_000019.10:54903358:CA:CACTCA
        Gene:
        NCR1 (Varview)
        Functional Consequence:
        intron_variant,genic_upstream_transcript_variant
        Validated:
        by frequency,by cluster
        MAF:
        CACT=0.000071/2 (TOMMO)
        CACG=0.000829/90 (GnomAD)
        HGVS:
        NC_000019.10:g.54903360_54903361insCGCA, NC_000019.10:g.54903360_54903361insCTCA, NW_004166865.1:g.877728_877729insCGCA, NW_004166865.1:g.877728_877729insCTCA, NW_003571061.2:g.615513_615514insCGCA, NW_003571061.2:g.615513_615514insCTCA, NW_003571061.1:g.615512_615513insCGCA, NW_003571061.1:g.615512_615513insCTCA, NW_003571055.2:g.548542_548543insCGCA, NW_003571055.2:g.548542_548543insCTCA, NW_003571055.1:g.548541_548542insCGCA, NW_003571055.1:g.548541_548542insCTCA, NW_003571059.2:g.821717_821718insCGCA, NW_003571059.2:g.821717_821718insCTCA, NW_003571056.2:g.883338_883339insCGCA, NW_003571056.2:g.883338_883339insCTCA, NW_003571057.2:g.910875_910876insCGCA, NW_003571057.2:g.910875_910876insCTCA, NW_003571058.2:g.885424_885425insCGCA, NW_003571058.2:g.885424_885425insCTCA, NT_187693.1:g.885834_885835insCGCA, NT_187693.1:g.885834_885835insCTCA, NC_000019.9:g.55414720_55414721insCGCA, NC_000019.9:g.55414720_55414721insCTCA, NW_003571060.1:g.807720_807721insCGCA, NW_003571060.1:g.807720_807721insCTCA, NW_003571054.1:g.806750_806751insCGCA, NW_003571054.1:g.806750_806751insCTCA, NT_187675.1:g.273599_273600insCGCA, NT_187675.1:g.273599_273600insCTCA, NT_187674.1:g.189380_189381insCGCA, NT_187674.1:g.189380_189381insCTCA, NT_187671.1:g.182307_182308insCGCA, NT_187671.1:g.182307_182308insCTCA, NT_187676.1:g.179310_179311insCGCA, NT_187676.1:g.179310_179311insCTCA, NT_187683.1:g.177578_177579insCGCA, NT_187683.1:g.177578_177579insCTCA, NW_016107304.1:g.232433_232434insCGCA, NW_016107304.1:g.232433_232434insCTCA, NT_187677.1:g.180727_180728insCGCA, NT_187677.1:g.180727_180728insCTCA, NW_016107312.1:g.8627_8628insCGTG, NW_016107312.1:g.8627_8628insAGTG

        4.

        rs1491558466 [Homo sapiens]
          Variant type:
          DEL
          Alleles:
          GC>- [Show Flanks]
          Chromosome:
          19:54772771 (GRCh38)
          19:55284223 (GRCh37)
          Canonical SPDI:
          NC_000019.10:54772770:GC:
          Gene:
          KIR2DL1 (Varview), LOC101928804 (Varview)
          Functional Consequence:
          2KB_upstream_variant,upstream_transcript_variant,intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          -=0./0 (ALFA)
          -=0.001522/193 (GnomAD)
          -=0.006133/173 (TOMMO)
          HGVS:
          NC_000019.10:g.54772771_54772772del, NW_004166865.1:g.747138_747139del, NG_051369.1:g.8564_8565del, NW_003571059.2:g.755607_755608del, NW_003571059.1:g.755606_755607del, NW_003571057.2:g.844884_844885del, NW_003571057.1:g.844883_844884del, NW_016107309.1:g.74378_74379del, NW_016107307.1:g.74338_74339del, NW_016107304.1:g.74381_74382del, NW_016107303.1:g.74349_74350del, NW_016107300.1:g.74404_74405del, NW_003571060.1:g.677105_677106del, NT_187693.1:g.755337_755338del, NC_000019.9:g.55284223_55284224del, NT_187685.1:g.95819_95820del, NT_187676.1:g.48685_48686del, NT_187673.1:g.96306_96307del, NT_187672.1:g.74349_74350del, NT_187669.1:g.96327_96328del, NT_187645.1:g.96343_96344del, NT_187643.1:g.96327_96328del, NT_187641.1:g.135653_135654del, NT_187639.1:g.96636_96637del, NT_187637.1:g.96067_96068del, NT_187671.1:g.51684_51685del, NW_016107305.1:g.74368_74369del, NW_016107301.1:g.74412_74413del, NW_003571054.1:g.678432_678433del, NT_187687.1:g.96128_96129del, NT_187683.1:g.46948_46949del, NT_187674.1:g.59611_59612del, NW_016107306.1:g.74186_74187del, NW_016107302.1:g.74381_74382del, NT_187686.1:g.96675_96676del, NT_187684.1:g.97819_97820del, NT_187675.1:g.115772_115773del, NT_187668.1:g.86225_86226del, NT_187640.1:g.85437_85438del, NT_187636.1:g.129977_129978del, NW_016107313.1:g.74402_74403del, NW_016107310.1:g.104755_104756del, NW_016107311.1:g.74372_74373del, NW_016107308.1:g.74359_74360del

          5.

          rs1491525446 has merged into rs1466580613 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            TA>-,TATA [Show Flanks]
            Chromosome:
            19:54903341 (GRCh38)
            19:55414701 (GRCh37)
            Canonical SPDI:
            NC_000019.10:54903336:TATATA:TATA,NC_000019.10:54903336:TATATA:TATATATA
            Gene:
            NCR1 (Varview)
            Functional Consequence:
            intron_variant,genic_upstream_transcript_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            TATATATA=0./0 (ALFA)
            -=0.000076/8 (GnomAD)
            -=0.000108/3 (TOMMO)
            HGVS:
            NC_000019.10:g.54903337TA[2], NC_000019.10:g.54903337TA[4], NW_004166865.1:g.877705TA[2], NW_004166865.1:g.877705TA[4], NW_003571061.2:g.615490TA[2], NW_003571061.2:g.615490TA[4], NW_003571061.1:g.615489TA[2], NW_003571061.1:g.615489TA[4], NW_003571055.2:g.548519TA[2], NW_003571055.2:g.548519TA[4], NW_003571055.1:g.548518TA[2], NW_003571055.1:g.548518TA[4], NW_003571059.2:g.821694TA[2], NW_003571059.2:g.821694TA[4], NW_003571056.2:g.883315TA[2], NW_003571056.2:g.883315TA[4], NW_003571057.2:g.910852TA[2], NW_003571057.2:g.910852TA[4], NW_003571058.2:g.885401TA[2], NW_003571058.2:g.885401TA[4], NT_187693.1:g.885811TA[2], NT_187693.1:g.885811TA[4], NC_000019.9:g.55414697TA[2], NC_000019.9:g.55414697TA[4], NW_003571060.1:g.807697TA[2], NW_003571060.1:g.807697TA[4], NW_003571054.1:g.806727TA[2], NW_003571054.1:g.806727TA[4], NT_187675.1:g.273576TA[2], NT_187675.1:g.273576TA[4], NT_187674.1:g.189357TA[2], NT_187674.1:g.189357TA[4], NT_187671.1:g.182284TA[2], NT_187671.1:g.182284TA[4], NT_187676.1:g.179287TA[2], NT_187676.1:g.179287TA[4], NT_187683.1:g.177555TA[2], NT_187683.1:g.177555TA[4], NW_016107304.1:g.232410TA[2], NW_016107304.1:g.232410TA[4], NT_187677.1:g.180704TA[2], NT_187677.1:g.180704TA[4], NW_016107312.1:g.8644TA[2], NW_016107312.1:g.8644TA[4]

            6.

            rs1491494928 has merged into rs199952856 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              AA>-,A,AAA [Show Flanks]
              Chromosome:
              19:54903705 (GRCh38)
              19:55415065 (GRCh37)
              Canonical SPDI:
              NC_000019.10:54903702:AAAA:AA,NC_000019.10:54903702:AAAA:AAA,NC_000019.10:54903702:AAAA:AAAAA
              Gene:
              NCR1 (Varview)
              Functional Consequence:
              genic_upstream_transcript_variant,intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              AAAAA=0./0 (ALFA)
              -=0.03691/22 (NorthernSweden)
              HGVS:
              NC_000019.10:g.54903705_54903706del, NC_000019.10:g.54903706del, NC_000019.10:g.54903706dup, NW_004166865.1:g.878073_878074del, NW_004166865.1:g.878074del, NW_004166865.1:g.878074dup, NW_003571061.2:g.615858_615859del, NW_003571061.2:g.615859del, NW_003571061.2:g.615859dup, NW_003571061.1:g.615857_615858del, NW_003571061.1:g.615858del, NW_003571061.1:g.615858dup, NW_003571055.2:g.548889_548890del, NW_003571055.2:g.548890del, NW_003571055.2:g.548890dup, NW_003571055.1:g.548888_548889del, NW_003571055.1:g.548889del, NW_003571055.1:g.548889dup, NW_003571059.2:g.822062_822063del, NW_003571059.2:g.822063del, NW_003571059.2:g.822063dup, NW_003571056.2:g.883683_883684del, NW_003571056.2:g.883684del, NW_003571056.2:g.883684dup, NW_003571057.2:g.911220_911221del, NW_003571057.2:g.911221del, NW_003571057.2:g.911221dup, NW_003571058.2:g.885769_885770del, NW_003571058.2:g.885770del, NW_003571058.2:g.885770dup, NT_187693.1:g.886179_886180del, NT_187693.1:g.886180del, NT_187693.1:g.886180dup, NC_000019.9:g.55415065_55415066del, NC_000019.9:g.55415066del, NC_000019.9:g.55415066dup, NW_003571060.1:g.808065_808066del, NW_003571060.1:g.808066del, NW_003571060.1:g.808066dup, NW_003571054.1:g.807095_807096del, NW_003571054.1:g.807096del, NW_003571054.1:g.807096dup, NT_187675.1:g.273944_273945del, NT_187675.1:g.273945del, NT_187675.1:g.273945dup, NT_187674.1:g.189725_189726del, NT_187674.1:g.189726del, NT_187674.1:g.189726dup, NT_187671.1:g.182652_182653del, NT_187671.1:g.182653del, NT_187671.1:g.182653dup, NT_187676.1:g.179655_179656del, NT_187676.1:g.179656del, NT_187676.1:g.179656dup, NT_187683.1:g.177923_177924del, NT_187683.1:g.177924del, NT_187683.1:g.177924dup, NW_016107304.1:g.232778_232779del, NW_016107304.1:g.232779del, NW_016107304.1:g.232779dup, NT_187677.1:g.181072_181073del, NT_187677.1:g.181073del, NT_187677.1:g.181073dup, NW_016107312.1:g.8282_8283del, NW_016107312.1:g.8283del, NW_016107312.1:g.8283dup

              7.

              rs1491474273 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                ->AA [Show Flanks]
                Chromosome:
                19:54903267 (GRCh38)
                19:55414628 (GRCh37)
                Canonical SPDI:
                NC_000019.10:54903267:A:AAA
                Gene:
                NCR1 (Varview)
                Functional Consequence:
                intron_variant,genic_upstream_transcript_variant
                Validated:
                by frequency,by alfa
                MAF:
                AAA=0./0 (ALFA)
                HGVS:

                8.

                rs1491473637 has merged into rs34625687 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTTTTTTT [Show Flanks]
                  Chromosome:
                  19:54879689 (GRCh38)
                  19:55391145 (GRCh37)
                  Canonical SPDI:
                  NC_000019.10:54879676:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000019.10:54879676:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000019.10:54879676:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000019.10:54879676:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000019.10:54879676:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000019.10:54879676:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000019.10:54879676:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000019.10:54879676:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
                  Gene:
                  FCAR (Varview)
                  Functional Consequence:
                  genic_upstream_transcript_variant,intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  TTTTTTTTTTTTTT=0./0 (ALFA)
                  T=0.1514/758 (1000Genomes)
                  HGVS:
                  NC_000019.10:g.54879689_54879693del, NC_000019.10:g.54879690_54879693del, NC_000019.10:g.54879691_54879693del, NC_000019.10:g.54879692_54879693del, NC_000019.10:g.54879693del, NC_000019.10:g.54879693dup, NC_000019.10:g.54879692_54879693dup, NC_000019.10:g.54879686_54879693dup, NW_004166865.1:g.854057_854061del, NW_004166865.1:g.854058_854061del, NW_004166865.1:g.854059_854061del, NW_004166865.1:g.854060_854061del, NW_004166865.1:g.854061del, NW_004166865.1:g.854061dup, NW_004166865.1:g.854060_854061dup, NW_004166865.1:g.854054_854061dup, NW_003571055.2:g.524957dup, NW_003571055.2:g.524954_524957del, NW_003571055.2:g.524955_524957del, NW_003571055.2:g.524956_524957del, NW_003571055.2:g.524957del, NW_003571055.2:g.524956_524957dup, NW_003571055.2:g.524955_524957dup, NW_003571055.2:g.524949_524957dup, NT_187693.1:g.862259_862263del, NT_187693.1:g.862260_862263del, NT_187693.1:g.862261_862263del, NT_187693.1:g.862262_862263del, NT_187693.1:g.862263del, NT_187693.1:g.862263dup, NT_187693.1:g.862262_862263dup, NT_187693.1:g.862256_862263dup, NC_000019.9:g.55391145_55391149del, NC_000019.9:g.55391146_55391149del, NC_000019.9:g.55391147_55391149del, NC_000019.9:g.55391148_55391149del, NC_000019.9:g.55391149del, NC_000019.9:g.55391149dup, NC_000019.9:g.55391148_55391149dup, NC_000019.9:g.55391142_55391149dup, NW_003571060.1:g.784066dup, NW_003571060.1:g.784063_784066del, NW_003571060.1:g.784064_784066del, NW_003571060.1:g.784065_784066del, NW_003571060.1:g.784066del, NW_003571060.1:g.784065_784066dup, NW_003571060.1:g.784064_784066dup, NW_003571060.1:g.784058_784066dup, NT_187675.1:g.249928_249932del, NT_187675.1:g.249929_249932del, NT_187675.1:g.249930_249932del, NT_187675.1:g.249931_249932del, NT_187675.1:g.249932del, NT_187675.1:g.249932dup, NT_187675.1:g.249931_249932dup, NT_187675.1:g.249925_249932dup, NT_187674.1:g.165709_165713del, NT_187674.1:g.165710_165713del, NT_187674.1:g.165711_165713del, NT_187674.1:g.165712_165713del, NT_187674.1:g.165713del, NT_187674.1:g.165713dup, NT_187674.1:g.165712_165713dup, NT_187674.1:g.165706_165713dup, NT_187671.1:g.158636_158640del, NT_187671.1:g.158637_158640del, NT_187671.1:g.158638_158640del, NT_187671.1:g.158639_158640del, NT_187671.1:g.158640del, NT_187671.1:g.158640dup, NT_187671.1:g.158639_158640dup, NT_187671.1:g.158633_158640dup, NT_187676.1:g.155639_155643del, NT_187676.1:g.155640_155643del, NT_187676.1:g.155641_155643del, NT_187676.1:g.155642_155643del, NT_187676.1:g.155643del, NT_187676.1:g.155643dup, NT_187676.1:g.155642_155643dup, NT_187676.1:g.155636_155643dup, NT_187683.1:g.153907_153911del, NT_187683.1:g.153908_153911del, NT_187683.1:g.153909_153911del, NT_187683.1:g.153910_153911del, NT_187683.1:g.153911del, NT_187683.1:g.153911dup, NT_187683.1:g.153910_153911dup, NT_187683.1:g.153904_153911dup, NT_187641.1:g.1517dup, NT_187641.1:g.1514_1517del, NT_187641.1:g.1515_1517del, NT_187641.1:g.1516_1517del, NT_187641.1:g.1517del, NT_187641.1:g.1516_1517dup, NT_187641.1:g.1515_1517dup, NT_187641.1:g.1509_1517dup, NW_016107304.1:g.208762_208766del, NW_016107304.1:g.208763_208766del, NW_016107304.1:g.208764_208766del, NW_016107304.1:g.208765_208766del, NW_016107304.1:g.208766del, NW_016107304.1:g.208766dup, NW_016107304.1:g.208765_208766dup, NW_016107304.1:g.208759_208766dup, NT_187677.1:g.157056_157060del, NT_187677.1:g.157057_157060del, NT_187677.1:g.157058_157060del, NT_187677.1:g.157059_157060del, NT_187677.1:g.157060del, NT_187677.1:g.157060dup, NT_187677.1:g.157059_157060dup, NT_187677.1:g.157053_157060dup, NW_016107312.1:g.32305_32309del, NW_016107312.1:g.32306_32309del, NW_016107312.1:g.32307_32309del, NW_016107312.1:g.32308_32309del, NW_016107312.1:g.32309del, NW_016107312.1:g.32309dup, NW_016107312.1:g.32308_32309dup, NW_016107312.1:g.32302_32309dup, NW_003571055.1:g.524956dup, NW_003571055.1:g.524953_524956del, NW_003571055.1:g.524954_524956del, NW_003571055.1:g.524955_524956del, NW_003571055.1:g.524956del, NW_003571055.1:g.524955_524956dup, NW_003571055.1:g.524954_524956dup, NW_003571055.1:g.524948_524956dup

                  9.

                  rs1491462763 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    CATATA>-,CATATACATATA [Show Flanks]
                    Chromosome:
                    19:54903343 (GRCh38)
                    19:55414703 (GRCh37)
                    Canonical SPDI:
                    NC_000019.10:54903337:ATATACATATA:ATATA,NC_000019.10:54903337:ATATACATATA:ATATACATATACATATA
                    Gene:
                    NCR1 (Varview)
                    Functional Consequence:
                    intron_variant,genic_upstream_transcript_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    ATATACATATACATATA=0./0 (ALFA)
                    -=0.000004/1 (TOPMED)
                    ATATAC=0.000009/1 (GnomAD)
                    HGVS:
                    NC_000019.10:g.54903343_54903348del, NC_000019.10:g.54903343_54903348dup, NW_004166865.1:g.877711_877716del, NW_004166865.1:g.877711_877716dup, NW_003571061.2:g.615496_615501del, NW_003571061.2:g.615496_615501dup, NW_003571061.1:g.615495_615500del, NW_003571061.1:g.615495_615500dup, NW_003571055.2:g.548525_548530del, NW_003571055.2:g.548525_548530dup, NW_003571055.1:g.548524_548529del, NW_003571055.1:g.548524_548529dup, NW_003571059.2:g.821700_821705del, NW_003571059.2:g.821700_821705dup, NW_003571056.2:g.883321_883326del, NW_003571056.2:g.883321_883326dup, NW_003571057.2:g.910858_910863del, NW_003571057.2:g.910858_910863dup, NW_003571058.2:g.885407_885412del, NW_003571058.2:g.885407_885412dup, NT_187693.1:g.885817_885822del, NT_187693.1:g.885817_885822dup, NC_000019.9:g.55414703_55414708del, NC_000019.9:g.55414703_55414708dup, NW_003571060.1:g.807703_807708del, NW_003571060.1:g.807703_807708dup, NW_003571054.1:g.806733_806738del, NW_003571054.1:g.806733_806738dup, NT_187675.1:g.273582_273587del, NT_187675.1:g.273582_273587dup, NT_187674.1:g.189363_189368del, NT_187674.1:g.189363_189368dup, NT_187671.1:g.182290_182295del, NT_187671.1:g.182290_182295dup, NT_187676.1:g.179293_179298del, NT_187676.1:g.179293_179298dup, NT_187683.1:g.177561_177566del, NT_187683.1:g.177561_177566dup, NW_016107304.1:g.232416_232421del, NW_016107304.1:g.232416_232421dup, NT_187677.1:g.180710_180715del, NT_187677.1:g.180710_180715dup, NW_016107312.1:g.8643_8648del, NW_016107312.1:g.8643_8648dup

                    10.

                    rs1491456462 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      CA>- [Show Flanks]
                      Chromosome:
                      19:54903453 (GRCh38)
                      19:55414813 (GRCh37)
                      Canonical SPDI:
                      NC_000019.10:54903451:ACA:A
                      Gene:
                      NCR1 (Varview)
                      Functional Consequence:
                      intron_variant,genic_upstream_transcript_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      A=0./0 (ALFA)
                      HGVS:

                      11.

                      rs1491435732 [Homo sapiens]
                        Variant type:
                        DEL
                        Alleles:
                        AT>- [Show Flanks]
                        Chromosome:
                        19:54878751 (GRCh38)
                        19:55390207 (GRCh37)
                        Canonical SPDI:
                        NC_000019.10:54878750:AT:
                        Gene:
                        FCAR (Varview)
                        Functional Consequence:
                        intron_variant,genic_upstream_transcript_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        -=0./0 (ALFA)
                        -=0.00004/1 (TOMMO)
                        HGVS:

                        12.

                        rs1491409048 [Homo sapiens]
                          Variant type:
                          DEL
                          Alleles:
                          TA>- [Show Flanks]
                          Chromosome:
                          19:54800177 (GRCh38)
                          19:55311632 (GRCh37)
                          Canonical SPDI:
                          NC_000019.10:54800176:TA:
                          Validated:
                          by frequency,by alfa
                          MAF:
                          -=0./0 (ALFA)
                          HGVS:
                          NC_000019.10:g.54800177_54800178del, NW_004166865.1:g.774545_774546del, NW_003571055.2:g.418033_418034del, NW_003571055.1:g.418032_418033del, NT_113949.2:g.89215_89216del, NT_187693.1:g.782746_782747del, NC_000019.9:g.55311632_55311633del, NW_003571060.1:g.704517dup, NW_003571060.1:g.704503del, NT_187675.1:g.143178_143179del, NT_187674.1:g.87023dup, NT_187674.1:g.87009del, NT_187671.1:g.79095dup, NT_187671.1:g.79081del, NT_187676.1:g.76094dup, NT_187676.1:g.76080del, NT_187683.1:g.74359dup, NT_187683.1:g.74345del, NT_187641.1:g.108248_108249del, NW_016107304.1:g.101794_101795del, NW_016107306.1:g.101601dup, NW_016107306.1:g.101587del, NT_187636.1:g.102572_102573del, NT_187677.1:g.77543_77544del, NW_016107313.1:g.101753dup, NW_016107313.1:g.101739del, NT_187639.1:g.69238dup, NT_187639.1:g.69240del, NT_187686.1:g.69270dup, NT_187686.1:g.69272del, NT_187673.1:g.68900_68901del, NT_187643.1:g.68929dup, NT_187643.1:g.68931del, NT_187645.1:g.68944dup, NT_187645.1:g.68946del, NT_187669.1:g.68929dup, NT_187669.1:g.68931del, NT_187687.1:g.68728_68729del, NT_187684.1:g.68709_68710del, NT_187637.1:g.68669dup, NT_187637.1:g.68671del, NW_016107301.1:g.101820_101821del, NT_187685.1:g.68422dup, NT_187685.1:g.68424del, NW_016107302.1:g.101791dup, NW_016107302.1:g.101776del, NW_016107307.1:g.101737_101738del, NW_016107300.1:g.101808_101809del, NW_016107309.1:g.101791dup, NW_016107309.1:g.101776del, NT_187668.1:g.58831dup, NT_187668.1:g.58833del, NT_187640.1:g.58031_58032del, NW_016107305.1:g.101778dup, NW_016107305.1:g.101764del, NT_187638.1:g.68840_68841del, NT_187670.1:g.96359_96360del, NT_187644.1:g.96286_96287del, NT_113949.1:g.53774_53775del, NT_187642.1:g.67367dup, NT_187642.1:g.67369del, NW_016107303.1:g.101775_101776del, NT_187672.1:g.101749dup, NT_187672.1:g.101735del, NW_016107314.1:g.88167_88168del, NW_016107310.1:g.132161_132162del

                          13.

                          rs1491391131 [Homo sapiens]
                            Variant type:
                            DEL
                            Alleles:
                            CA>- [Show Flanks]
                            Chromosome:
                            19:54869711 (GRCh38)
                            19:55381167 (GRCh37)
                            Canonical SPDI:
                            NC_000019.10:54869710:CA:
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            -=0.00287/34 (ALFA)
                            -=0.00173/48 (TOMMO)
                            HGVS:
                            NC_000019.10:g.54869711_54869712del, NW_004166865.1:g.844079_844080del, NW_003571055.2:g.515001dup, NW_003571055.2:g.514981del, NW_003571059.2:g.788318dup, NW_003571059.2:g.788298del, NW_003571058.2:g.851670dup, NW_003571058.2:g.851649del, NT_187693.1:g.852281_852282del, NC_000019.9:g.55381167_55381168del, NW_003571060.1:g.774107dup, NW_003571060.1:g.774086del, NT_187675.1:g.239950_239951del, NT_187674.1:g.155731_155732del, NT_187671.1:g.148658_148659del, NT_187676.1:g.145661_145662del, NT_187683.1:g.143929_143930del, NT_187641.1:g.11478dup, NT_187641.1:g.11479del, NW_016107304.1:g.198806dup, NW_016107304.1:g.198785del, NW_016107306.1:g.170309_170310del, NT_187636.1:g.5804dup, NT_187636.1:g.5805del, NW_016107311.1:g.90835_90836del, NW_016107308.1:g.92118dup, NW_016107308.1:g.92098del, NW_016107312.1:g.42274_42275del, NW_003571055.1:g.515000dup, NW_003571055.1:g.514980del, NW_003571059.1:g.788317dup, NW_003571059.1:g.788297del, NW_003571058.1:g.851669dup, NW_003571058.1:g.851648del

                            14.

                            rs1491381846 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              G>AA,GG [Show Flanks]
                              Chromosome:
                              19:54911358 (GRCh38)
                              19:55422718 (GRCh37)
                              Canonical SPDI:
                              NC_000019.10:54911357:G:AA,NC_000019.10:54911357:G:GG
                              Gene:
                              NCR1 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              GG=0./0 (ALFA)
                              -=0.000008/1 (GnomAD)
                              -=0.000015/4 (TOPMED)
                              HGVS:
                              NC_000019.10:g.54911358delinsAA, NC_000019.10:g.54911358dup, NW_004166865.1:g.885726delinsAA, NW_004166865.1:g.885726dup, NW_003571061.2:g.623511A>G, NW_003571061.2:g.623516dup, NW_003571061.2:g.623511delinsGG, NW_003571061.1:g.623510A>G, NW_003571061.1:g.623515dup, NW_003571061.1:g.623510delinsGG, NW_003571055.2:g.556541A>G, NW_003571055.2:g.556546dup, NW_003571055.2:g.556541delinsGG, NW_003571055.1:g.556540A>G, NW_003571055.1:g.556545dup, NW_003571055.1:g.556540delinsGG, NW_003571059.2:g.829715A>G, NW_003571059.2:g.829720dup, NW_003571059.2:g.829715delinsGG, NW_003571056.2:g.891336A>G, NW_003571056.2:g.891341dup, NW_003571056.2:g.891336delinsGG, NW_003571057.2:g.918873A>G, NW_003571057.2:g.918878dup, NW_003571057.2:g.918873delinsGG, NW_003571058.2:g.893422A>G, NW_003571058.2:g.893427dup, NW_003571058.2:g.893422delinsGG, NT_187693.1:g.893832A>G, NT_187693.1:g.893837dup, NT_187693.1:g.893832delinsGG, NC_000019.9:g.55422718A>G, NC_000019.9:g.55422723dup, NC_000019.9:g.55422718delinsGG, NW_003571060.1:g.815712A>G, NW_003571060.1:g.815717dup, NW_003571060.1:g.815712delinsGG, NW_003571054.1:g.814748A>G, NW_003571054.1:g.814753dup, NW_003571054.1:g.814748delinsGG, NT_187675.1:g.281597delinsAA, NT_187675.1:g.281597dup, NT_187674.1:g.197378delinsAA, NT_187674.1:g.197378dup, NT_187671.1:g.190305delinsAA, NT_187671.1:g.190305dup, NT_187676.1:g.187308delinsAA, NT_187676.1:g.187308dup, NT_187683.1:g.185576delinsAA, NT_187683.1:g.185576dup, NW_016107304.1:g.240431delinsAA, NW_016107304.1:g.240431dup, NT_187677.1:g.188725delinsAA, NT_187677.1:g.188725dup, NW_016107312.1:g.628delinsTT, NW_016107312.1:g.628dup

                              15.

                              rs1491375659 has merged into rs71195798 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                TA>-,TATA,TATATA [Show Flanks]
                                Chromosome:
                                19:54761517 (GRCh38)
                                19:55272969 (GRCh37)
                                Canonical SPDI:
                                NC_000019.10:54761503:ATATATATATATATA:ATATATATATATA,NC_000019.10:54761503:ATATATATATATATA:ATATATATATATATATA,NC_000019.10:54761503:ATATATATATATATA:ATATATATATATATATATA
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                ATATATATATATATATATA=0./0 (ALFA)
                                AT=0.01031/6 (NorthernSweden)
                                HGVS:
                                NC_000019.10:g.54761505TA[6], NC_000019.10:g.54761505TA[8], NC_000019.10:g.54761505TA[9], NW_004166865.1:g.735872TA[6], NW_004166865.1:g.735872TA[8], NW_004166865.1:g.735872TA[9], NG_033793.2:g.6850TA[6], NG_033793.2:g.6850TA[8], NG_033793.2:g.6850TA[9], NW_003571059.2:g.744341TA[6], NW_003571059.2:g.744341TA[8], NW_003571059.2:g.744341TA[9], NW_003571059.1:g.744340TA[6], NW_003571059.1:g.744340TA[8], NW_003571059.1:g.744340TA[9], NW_016107309.1:g.63112TA[6], NW_016107309.1:g.63112TA[8], NW_016107309.1:g.63112TA[9], NW_016107308.1:g.63093TA[6], NW_016107308.1:g.63093TA[8], NW_016107308.1:g.63093TA[9], NW_016107307.1:g.63072TA[6], NW_016107307.1:g.63072TA[8], NW_016107307.1:g.63072TA[9], NW_016107304.1:g.63115TA[6], NW_016107304.1:g.63115TA[8], NW_016107304.1:g.63115TA[9], NW_016107303.1:g.63083TA[6], NW_016107303.1:g.63083TA[8], NW_016107303.1:g.63083TA[9], NW_016107300.1:g.63138TA[6], NW_016107300.1:g.63138TA[8], NW_016107300.1:g.63138TA[9], NW_003571060.1:g.665839TA[6], NW_003571060.1:g.665839TA[8], NW_003571060.1:g.665839TA[9], NT_187693.1:g.744071TA[6], NT_187693.1:g.744071TA[8], NT_187693.1:g.744071TA[9], NC_000019.9:g.55272957TA[6], NC_000019.9:g.55272957TA[8], NC_000019.9:g.55272957TA[9], NT_187685.1:g.107074AT[6], NT_187685.1:g.107074AT[8], NT_187685.1:g.107074AT[9], NT_187676.1:g.37419TA[6], NT_187676.1:g.37419TA[8], NT_187676.1:g.37419TA[9], NT_187673.1:g.107561AT[6], NT_187673.1:g.107561AT[8], NT_187673.1:g.107561AT[9], NT_187672.1:g.63083TA[6], NT_187672.1:g.63083TA[8], NT_187672.1:g.63083TA[9], NT_187671.1:g.40418TA[6], NT_187671.1:g.40418TA[8], NT_187671.1:g.40418TA[9], NT_187669.1:g.107582AT[6], NT_187669.1:g.107582AT[8], NT_187669.1:g.107582AT[9], NT_187645.1:g.107598AT[6], NT_187645.1:g.107598AT[8], NT_187645.1:g.107598AT[9], NT_187643.1:g.107582AT[6], NT_187643.1:g.107582AT[8], NT_187643.1:g.107582AT[9], NT_187641.1:g.146908AT[6], NT_187641.1:g.146908AT[8], NT_187641.1:g.146908AT[9], NT_187639.1:g.107891AT[6], NT_187639.1:g.107891AT[8], NT_187639.1:g.107891AT[9], NT_187637.1:g.107322AT[6], NT_187637.1:g.107322AT[8], NT_187637.1:g.107322AT[9], NW_016107313.1:g.63132TA[6], NW_016107313.1:g.63132TA[8], NW_016107313.1:g.63132TA[9], NW_016107311.1:g.63093TA[6], NW_016107311.1:g.63093TA[8], NW_016107311.1:g.63093TA[9], NW_016107305.1:g.63099TA[6], NW_016107305.1:g.63099TA[8], NW_016107305.1:g.63099TA[9], NW_016107302.1:g.63112TA[6], NW_016107302.1:g.63112TA[8], NW_016107302.1:g.63112TA[9], NW_003571054.1:g.667163TA[6], NW_003571054.1:g.667163TA[8], NW_003571054.1:g.667163TA[9], NT_187687.1:g.107386AT[6], NT_187687.1:g.107386AT[8], NT_187687.1:g.107386AT[9], NT_187674.1:g.48354C>T, NT_187674.1:g.48354CA[2], NT_187674.1:g.48354delinsTAT, NT_187674.1:g.48354delinsTATAT, NT_187668.1:g.97484AT[6], NT_187668.1:g.97484AT[8], NT_187668.1:g.97484AT[9], NW_016107310.1:g.93483TA[6], NW_016107310.1:g.93483TA[8], NW_016107310.1:g.93483TA[9], NW_016107306.1:g.62913TA[6], NW_016107306.1:g.62913TA[8], NW_016107306.1:g.62913TA[9], NW_016107301.1:g.63143TA[6], NW_016107301.1:g.63143TA[8], NW_016107301.1:g.63143TA[9], NT_187686.1:g.107934G>A, NT_187686.1:g.107930GT[2], NT_187686.1:g.107934delinsATA, NT_187686.1:g.107934delinsATATA, NT_187684.1:g.109077AT[6], NT_187684.1:g.109077AT[8], NT_187684.1:g.109077AT[9], NT_187683.1:g.35680TA[6], NT_187683.1:g.35680TA[8], NT_187683.1:g.35680TA[9], NT_187675.1:g.104500TA[6], NT_187675.1:g.104500TA[8], NT_187675.1:g.104500TA[9], NT_187640.1:g.96699AT[6], NT_187640.1:g.96699AT[8], NT_187640.1:g.96699AT[9], NT_187636.1:g.141238AT[6], NT_187636.1:g.141238AT[8], NT_187636.1:g.141238AT[9], NW_003571057.2:g.833618TA[6], NW_003571057.2:g.833618TA[8], NW_003571057.2:g.833618TA[9], NW_003571057.1:g.833617TA[6], NW_003571057.1:g.833617TA[8], NW_003571057.1:g.833617TA[9]

                                16.

                                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

                                  17.

                                  rs1491355321 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    ->A [Show Flanks]
                                    Chromosome:
                                    19:54801324 (GRCh38)
                                    19:55312780 (GRCh37)
                                    Canonical SPDI:
                                    NC_000019.10:54801324:A:AA
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    AA=0./0 (ALFA)
                                    A=0.000036/5 (GnomAD)
                                    A=0.000042/11 (TOPMED)
                                    HGVS:
                                    NC_000019.10:g.54801325dup, NW_004166865.1:g.775693dup, NW_003571055.2:g.419180dup, NW_003571055.1:g.419179dup, NT_113949.2:g.88069dup, NT_187693.1:g.783894dup, NC_000019.9:g.55312780dup, NW_003571060.1:g.705647dup, NT_187675.1:g.144325dup, NT_187674.1:g.88153dup, NT_187671.1:g.80224dup, NT_187676.1:g.77224dup, NT_187683.1:g.75489dup, NT_187641.1:g.107102dup, NW_016107304.1:g.102941dup, NW_016107306.1:g.102731dup, NT_187636.1:g.101426dup, NT_187677.1:g.78691dup, NW_016107313.1:g.102883dup, NT_187639.1:g.68095dup, NT_187686.1:g.68126dup, NT_187673.1:g.67753dup, NT_187643.1:g.67786dup, NT_187645.1:g.67801dup, NT_187669.1:g.67786dup, NT_187687.1:g.67581dup, NT_187684.1:g.67562dup, NT_187637.1:g.67525dup, NW_016107301.1:g.102968dup, NT_187685.1:g.67278dup, NW_016107302.1:g.102921dup, NW_016107307.1:g.102883dup, NW_016107300.1:g.102956dup, NW_016107309.1:g.102921dup, NT_187668.1:g.57687dup, NT_187640.1:g.56884dup, NW_016107305.1:g.102908dup, NT_187638.1:g.67693dup, NT_187670.1:g.95213dup, NT_187644.1:g.95140dup, NT_113949.1:g.54921dup, NT_187642.1:g.66224dup, NW_016107303.1:g.102922dup, NT_187672.1:g.102879dup, NW_016107314.1:g.89315dup, NW_016107310.1:g.133308dup

                                    18.

                                    rs1491344481 [Homo sapiens]
                                      Variant type:
                                      DELINS
                                      Alleles:
                                      ->CGTATA [Show Flanks]
                                      Chromosome:
                                      19:54903344 (GRCh38)
                                      19:55414705 (GRCh37)
                                      Canonical SPDI:
                                      NC_000019.10:54903344:TATA:TATACGTATA
                                      Gene:
                                      NCR1 (Varview)
                                      Functional Consequence:
                                      intron_variant,genic_upstream_transcript_variant
                                      Validated:
                                      by frequency,by cluster
                                      MAF:
                                      TATACG=0.000548/60 (GnomAD)
                                      HGVS:
                                      NC_000019.10:g.54903345_54903348TA[2]CGTATA[1], NW_004166865.1:g.877713_877716TA[2]CGTATA[1], NW_003571061.2:g.615498_615501TA[2]CGTATA[1], NW_003571061.1:g.615497_615500TA[2]CGTATA[1], NW_003571055.2:g.548527_548530TA[2]CGTATA[1], NW_003571055.1:g.548526_548529TA[2]CGTATA[1], NW_003571059.2:g.821702_821705TA[2]CGTATA[1], NW_003571056.2:g.883323_883326TA[2]CGTATA[1], NW_003571057.2:g.910860_910863TA[2]CGTATA[1], NW_003571058.2:g.885409_885412TA[2]CGTATA[1], NT_187693.1:g.885819_885822TA[2]CGTATA[1], NC_000019.9:g.55414705_55414708TA[2]CGTATA[1], NW_003571060.1:g.807705_807708TA[2]CGTATA[1], NW_003571054.1:g.806735_806738TA[2]CGTATA[1], NT_187675.1:g.273584_273587TA[2]CGTATA[1], NT_187674.1:g.189365_189368TA[2]CGTATA[1], NT_187671.1:g.182292_182295TA[2]CGTATA[1], NT_187676.1:g.179295_179298TA[2]CGTATA[1], NT_187683.1:g.177563_177566TA[2]CGTATA[1], NW_016107304.1:g.232418_232421TA[2]CGTATA[1], NT_187677.1:g.180712_180715TA[2]CGTATA[1], NW_016107312.1:g.8638_8641TA[2]CGTATA[1]

                                      19.

                                      rs1491330532 has merged into rs35959167 [Homo sapiens]
                                        Variant type:
                                        DELINS
                                        Alleles:
                                        AAAAAAAAAAAAAA>-,A,AAA,AAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                                        Chromosome:
                                        19:54869720 (GRCh38)
                                        19:55381176 (GRCh37)
                                        Canonical SPDI:
                                        NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:54869711:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        AAAAAAAA=0./0 (ALFA)
                                        HGVS:
                                        NC_000019.10:g.54869720_54869733del, NC_000019.10:g.54869721_54869733del, NC_000019.10:g.54869723_54869733del, NC_000019.10:g.54869724_54869733del, NC_000019.10:g.54869726_54869733del, NC_000019.10:g.54869727_54869733del, NC_000019.10:g.54869728_54869733del, NC_000019.10:g.54869729_54869733del, NC_000019.10:g.54869730_54869733del, NC_000019.10:g.54869731_54869733del, NC_000019.10:g.54869732_54869733del, NC_000019.10:g.54869733del, NC_000019.10:g.54869733dup, NC_000019.10:g.54869732_54869733dup, NC_000019.10:g.54869731_54869733dup, NC_000019.10:g.54869730_54869733dup, NC_000019.10:g.54869729_54869733dup, NC_000019.10:g.54869728_54869733dup, NC_000019.10:g.54869727_54869733dup, NC_000019.10:g.54869726_54869733dup, NC_000019.10:g.54869725_54869733dup, NC_000019.10:g.54869724_54869733dup, NC_000019.10:g.54869717_54869733dup, NC_000019.10:g.54869733_54869734insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_004166865.1:g.844088_844101del, NW_004166865.1:g.844089_844101del, NW_004166865.1:g.844091_844101del, NW_004166865.1:g.844092_844101del, NW_004166865.1:g.844094_844101del, NW_004166865.1:g.844095_844101del, NW_004166865.1:g.844096_844101del, NW_004166865.1:g.844097_844101del, NW_004166865.1:g.844098_844101del, NW_004166865.1:g.844099_844101del, NW_004166865.1:g.844100_844101del, NW_004166865.1:g.844101del, NW_004166865.1:g.844101dup, NW_004166865.1:g.844100_844101dup, NW_004166865.1:g.844099_844101dup, NW_004166865.1:g.844098_844101dup, NW_004166865.1:g.844097_844101dup, NW_004166865.1:g.844096_844101dup, NW_004166865.1:g.844095_844101dup, NW_004166865.1:g.844094_844101dup, NW_004166865.1:g.844093_844101dup, NW_004166865.1:g.844092_844101dup, NW_004166865.1:g.844085_844101dup, NW_004166865.1:g.844101_844102insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_003571055.2:g.515000_515001dup, NW_003571055.2:g.514990_515001del, NW_003571055.2:g.514991_515001del, NW_003571055.2:g.514993_515001del, NW_003571055.2:g.514994_515001del, NW_003571055.2:g.514996_515001del, NW_003571055.2:g.514997_515001del, NW_003571055.2:g.514998_515001del, NW_003571055.2:g.514999_515001del, NW_003571055.2:g.515000_515001del, NW_003571055.2:g.515001del, NW_003571055.2:g.515001dup, NW_003571055.2:g.514999_515001dup, NW_003571055.2:g.514998_515001dup, NW_003571055.2:g.514997_515001dup, NW_003571055.2:g.514996_515001dup, NW_003571055.2:g.514995_515001dup, NW_003571055.2:g.514994_515001dup, NW_003571055.2:g.514993_515001dup, NW_003571055.2:g.514992_515001dup, NW_003571055.2:g.514991_515001dup, NW_003571055.2:g.514990_515001dup, NW_003571055.2:g.514983_515001dup, NW_003571055.2:g.515001_515002insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_003571059.2:g.788317_788318dup, NW_003571059.2:g.788307_788318del, NW_003571059.2:g.788308_788318del, NW_003571059.2:g.788310_788318del, NW_003571059.2:g.788311_788318del, NW_003571059.2:g.788313_788318del, NW_003571059.2:g.788314_788318del, NW_003571059.2:g.788315_788318del, NW_003571059.2:g.788316_788318del, NW_003571059.2:g.788317_788318del, NW_003571059.2:g.788318del, NW_003571059.2:g.788318dup, NW_003571059.2:g.788316_788318dup, NW_003571059.2:g.788315_788318dup, NW_003571059.2:g.788314_788318dup, NW_003571059.2:g.788313_788318dup, NW_003571059.2:g.788312_788318dup, NW_003571059.2:g.788311_788318dup, NW_003571059.2:g.788310_788318dup, NW_003571059.2:g.788309_788318dup, NW_003571059.2:g.788308_788318dup, NW_003571059.2:g.788307_788318dup, NW_003571059.2:g.788300_788318dup, NW_003571059.2:g.788318_788319insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_003571058.2:g.851670dup, NW_003571058.2:g.851658_851670del, NW_003571058.2:g.851659_851670del, NW_003571058.2:g.851661_851670del, NW_003571058.2:g.851662_851670del, NW_003571058.2:g.851664_851670del, NW_003571058.2:g.851665_851670del, NW_003571058.2:g.851666_851670del, NW_003571058.2:g.851667_851670del, NW_003571058.2:g.851668_851670del, NW_003571058.2:g.851669_851670del, NW_003571058.2:g.851670del, NW_003571058.2:g.851669_851670dup, NW_003571058.2:g.851668_851670dup, NW_003571058.2:g.851667_851670dup, NW_003571058.2:g.851666_851670dup, NW_003571058.2:g.851665_851670dup, NW_003571058.2:g.851664_851670dup, NW_003571058.2:g.851663_851670dup, NW_003571058.2:g.851662_851670dup, NW_003571058.2:g.851661_851670dup, NW_003571058.2:g.851660_851670dup, NW_003571058.2:g.851653_851670dup, NW_003571058.2:g.851670_851671insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187693.1:g.852290_852303del, NT_187693.1:g.852291_852303del, NT_187693.1:g.852293_852303del, NT_187693.1:g.852294_852303del, NT_187693.1:g.852296_852303del, NT_187693.1:g.852297_852303del, NT_187693.1:g.852298_852303del, NT_187693.1:g.852299_852303del, NT_187693.1:g.852300_852303del, NT_187693.1:g.852301_852303del, NT_187693.1:g.852302_852303del, NT_187693.1:g.852303del, NT_187693.1:g.852303dup, NT_187693.1:g.852302_852303dup, NT_187693.1:g.852301_852303dup, NT_187693.1:g.852300_852303dup, NT_187693.1:g.852299_852303dup, NT_187693.1:g.852298_852303dup, NT_187693.1:g.852297_852303dup, NT_187693.1:g.852296_852303dup, NT_187693.1:g.852295_852303dup, NT_187693.1:g.852294_852303dup, NT_187693.1:g.852287_852303dup, NT_187693.1:g.852303_852304insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.55381176_55381189del, NC_000019.9:g.55381177_55381189del, NC_000019.9:g.55381179_55381189del, NC_000019.9:g.55381180_55381189del, NC_000019.9:g.55381182_55381189del, NC_000019.9:g.55381183_55381189del, NC_000019.9:g.55381184_55381189del, NC_000019.9:g.55381185_55381189del, NC_000019.9:g.55381186_55381189del, NC_000019.9:g.55381187_55381189del, NC_000019.9:g.55381188_55381189del, NC_000019.9:g.55381189del, NC_000019.9:g.55381189dup, NC_000019.9:g.55381188_55381189dup, NC_000019.9:g.55381187_55381189dup, NC_000019.9:g.55381186_55381189dup, NC_000019.9:g.55381185_55381189dup, NC_000019.9:g.55381184_55381189dup, NC_000019.9:g.55381183_55381189dup, NC_000019.9:g.55381182_55381189dup, NC_000019.9:g.55381181_55381189dup, NC_000019.9:g.55381180_55381189dup, NC_000019.9:g.55381173_55381189dup, NC_000019.9:g.55381189_55381190insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_003571060.1:g.774107dup, NW_003571060.1:g.774095_774107del, NW_003571060.1:g.774096_774107del, NW_003571060.1:g.774098_774107del, NW_003571060.1:g.774099_774107del, NW_003571060.1:g.774101_774107del, NW_003571060.1:g.774102_774107del, NW_003571060.1:g.774103_774107del, NW_003571060.1:g.774104_774107del, NW_003571060.1:g.774105_774107del, NW_003571060.1:g.774106_774107del, NW_003571060.1:g.774107del, NW_003571060.1:g.774106_774107dup, NW_003571060.1:g.774105_774107dup, NW_003571060.1:g.774104_774107dup, NW_003571060.1:g.774103_774107dup, NW_003571060.1:g.774102_774107dup, NW_003571060.1:g.774101_774107dup, NW_003571060.1:g.774100_774107dup, NW_003571060.1:g.774099_774107dup, NW_003571060.1:g.774098_774107dup, NW_003571060.1:g.774097_774107dup, NW_003571060.1:g.774090_774107dup, NW_003571060.1:g.774107_774108insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187675.1:g.239959_239972del, NT_187675.1:g.239960_239972del, NT_187675.1:g.239962_239972del, NT_187675.1:g.239963_239972del, NT_187675.1:g.239965_239972del, NT_187675.1:g.239966_239972del, NT_187675.1:g.239967_239972del, NT_187675.1:g.239968_239972del, NT_187675.1:g.239969_239972del, NT_187675.1:g.239970_239972del, NT_187675.1:g.239971_239972del, NT_187675.1:g.239972del, NT_187675.1:g.239972dup, NT_187675.1:g.239971_239972dup, NT_187675.1:g.239970_239972dup, NT_187675.1:g.239969_239972dup, NT_187675.1:g.239968_239972dup, NT_187675.1:g.239967_239972dup, NT_187675.1:g.239966_239972dup, NT_187675.1:g.239965_239972dup, NT_187675.1:g.239964_239972dup, NT_187675.1:g.239963_239972dup, NT_187675.1:g.239956_239972dup, NT_187675.1:g.239972_239973insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187674.1:g.155740_155753del, NT_187674.1:g.155741_155753del, NT_187674.1:g.155743_155753del, NT_187674.1:g.155744_155753del, NT_187674.1:g.155746_155753del, NT_187674.1:g.155747_155753del, NT_187674.1:g.155748_155753del, NT_187674.1:g.155749_155753del, NT_187674.1:g.155750_155753del, NT_187674.1:g.155751_155753del, NT_187674.1:g.155752_155753del, NT_187674.1:g.155753del, NT_187674.1:g.155753dup, NT_187674.1:g.155752_155753dup, NT_187674.1:g.155751_155753dup, NT_187674.1:g.155750_155753dup, NT_187674.1:g.155749_155753dup, NT_187674.1:g.155748_155753dup, NT_187674.1:g.155747_155753dup, NT_187674.1:g.155746_155753dup, NT_187674.1:g.155745_155753dup, NT_187674.1:g.155744_155753dup, NT_187674.1:g.155737_155753dup, NT_187674.1:g.155753_155754insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187671.1:g.148667_148680del, NT_187671.1:g.148668_148680del, NT_187671.1:g.148670_148680del, NT_187671.1:g.148671_148680del, NT_187671.1:g.148673_148680del, NT_187671.1:g.148674_148680del, NT_187671.1:g.148675_148680del, NT_187671.1:g.148676_148680del, NT_187671.1:g.148677_148680del, NT_187671.1:g.148678_148680del, NT_187671.1:g.148679_148680del, NT_187671.1:g.148680del, NT_187671.1:g.148680dup, NT_187671.1:g.148679_148680dup, NT_187671.1:g.148678_148680dup, NT_187671.1:g.148677_148680dup, NT_187671.1:g.148676_148680dup, NT_187671.1:g.148675_148680dup, NT_187671.1:g.148674_148680dup, NT_187671.1:g.148673_148680dup, NT_187671.1:g.148672_148680dup, NT_187671.1:g.148671_148680dup, NT_187671.1:g.148664_148680dup, NT_187671.1:g.148680_148681insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187676.1:g.145670_145683del, NT_187676.1:g.145671_145683del, NT_187676.1:g.145673_145683del, NT_187676.1:g.145674_145683del, NT_187676.1:g.145676_145683del, NT_187676.1:g.145677_145683del, NT_187676.1:g.145678_145683del, NT_187676.1:g.145679_145683del, NT_187676.1:g.145680_145683del, NT_187676.1:g.145681_145683del, NT_187676.1:g.145682_145683del, NT_187676.1:g.145683del, NT_187676.1:g.145683dup, NT_187676.1:g.145682_145683dup, NT_187676.1:g.145681_145683dup, NT_187676.1:g.145680_145683dup, NT_187676.1:g.145679_145683dup, NT_187676.1:g.145678_145683dup, NT_187676.1:g.145677_145683dup, NT_187676.1:g.145676_145683dup, NT_187676.1:g.145675_145683dup, NT_187676.1:g.145674_145683dup, NT_187676.1:g.145667_145683dup, NT_187676.1:g.145683_145684insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187683.1:g.143938_143951del, NT_187683.1:g.143939_143951del, NT_187683.1:g.143941_143951del, NT_187683.1:g.143942_143951del, NT_187683.1:g.143944_143951del, NT_187683.1:g.143945_143951del, NT_187683.1:g.143946_143951del, NT_187683.1:g.143947_143951del, NT_187683.1:g.143948_143951del, NT_187683.1:g.143949_143951del, NT_187683.1:g.143950_143951del, NT_187683.1:g.143951del, NT_187683.1:g.143951dup, NT_187683.1:g.143950_143951dup, NT_187683.1:g.143949_143951dup, NT_187683.1:g.143948_143951dup, NT_187683.1:g.143947_143951dup, NT_187683.1:g.143946_143951dup, NT_187683.1:g.143945_143951dup, NT_187683.1:g.143944_143951dup, NT_187683.1:g.143943_143951dup, NT_187683.1:g.143942_143951dup, NT_187683.1:g.143935_143951dup, NT_187683.1:g.143951_143952insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187641.1:g.11477_11478dup, NT_187641.1:g.11467_11478del, NT_187641.1:g.11468_11478del, NT_187641.1:g.11470_11478del, NT_187641.1:g.11471_11478del, NT_187641.1:g.11473_11478del, NT_187641.1:g.11474_11478del, NT_187641.1:g.11475_11478del, NT_187641.1:g.11476_11478del, NT_187641.1:g.11477_11478del, NT_187641.1:g.11478del, NT_187641.1:g.11478dup, NT_187641.1:g.11476_11478dup, NT_187641.1:g.11475_11478dup, NT_187641.1:g.11474_11478dup, NT_187641.1:g.11473_11478dup, NT_187641.1:g.11472_11478dup, NT_187641.1:g.11471_11478dup, NT_187641.1:g.11470_11478dup, NT_187641.1:g.11469_11478dup, NT_187641.1:g.11468_11478dup, NT_187641.1:g.11467_11478dup, NT_187641.1:g.11460_11478dup, NT_187641.1:g.11478_11479insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_016107304.1:g.198806dup, NW_016107304.1:g.198794_198806del, NW_016107304.1:g.198795_198806del, NW_016107304.1:g.198797_198806del, NW_016107304.1:g.198798_198806del, NW_016107304.1:g.198800_198806del, NW_016107304.1:g.198801_198806del, NW_016107304.1:g.198802_198806del, NW_016107304.1:g.198803_198806del, NW_016107304.1:g.198804_198806del, NW_016107304.1:g.198805_198806del, NW_016107304.1:g.198806del, NW_016107304.1:g.198805_198806dup, NW_016107304.1:g.198804_198806dup, NW_016107304.1:g.198803_198806dup, NW_016107304.1:g.198802_198806dup, NW_016107304.1:g.198801_198806dup, NW_016107304.1:g.198800_198806dup, NW_016107304.1:g.198799_198806dup, NW_016107304.1:g.198798_198806dup, NW_016107304.1:g.198797_198806dup, NW_016107304.1:g.198796_198806dup, NW_016107304.1:g.198789_198806dup, NW_016107304.1:g.198806_198807insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_016107306.1:g.170318_170331del, NW_016107306.1:g.170319_170331del, NW_016107306.1:g.170321_170331del, NW_016107306.1:g.170322_170331del, NW_016107306.1:g.170324_170331del, NW_016107306.1:g.170325_170331del, NW_016107306.1:g.170326_170331del, NW_016107306.1:g.170327_170331del, NW_016107306.1:g.170328_170331del, NW_016107306.1:g.170329_170331del, NW_016107306.1:g.170330_170331del, NW_016107306.1:g.170331del, NW_016107306.1:g.170331dup, NW_016107306.1:g.170330_170331dup, NW_016107306.1:g.170329_170331dup, NW_016107306.1:g.170328_170331dup, NW_016107306.1:g.170327_170331dup, NW_016107306.1:g.170326_170331dup, NW_016107306.1:g.170325_170331dup, NW_016107306.1:g.170324_170331dup, NW_016107306.1:g.170323_170331dup, NW_016107306.1:g.170322_170331dup, NW_016107306.1:g.170315_170331dup, NW_016107306.1:g.170331_170332insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187636.1:g.5803_5804dup, NT_187636.1:g.5793_5804del, NT_187636.1:g.5794_5804del, NT_187636.1:g.5796_5804del, NT_187636.1:g.5797_5804del, NT_187636.1:g.5799_5804del, NT_187636.1:g.5800_5804del, NT_187636.1:g.5801_5804del, NT_187636.1:g.5802_5804del, NT_187636.1:g.5803_5804del, NT_187636.1:g.5804del, NT_187636.1:g.5804dup, NT_187636.1:g.5802_5804dup, NT_187636.1:g.5801_5804dup, NT_187636.1:g.5800_5804dup, NT_187636.1:g.5799_5804dup, NT_187636.1:g.5798_5804dup, NT_187636.1:g.5797_5804dup, NT_187636.1:g.5796_5804dup, NT_187636.1:g.5795_5804dup, NT_187636.1:g.5794_5804dup, NT_187636.1:g.5793_5804dup, NT_187636.1:g.5786_5804dup, NT_187636.1:g.5804_5805insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187677.1:g.147087_147100del, NT_187677.1:g.147088_147100del, NT_187677.1:g.147090_147100del, NT_187677.1:g.147091_147100del, NT_187677.1:g.147093_147100del, NT_187677.1:g.147094_147100del, NT_187677.1:g.147095_147100del, NT_187677.1:g.147096_147100del, NT_187677.1:g.147097_147100del, NT_187677.1:g.147098_147100del, NT_187677.1:g.147099_147100del, NT_187677.1:g.147100del, NT_187677.1:g.147100dup, NT_187677.1:g.147099_147100dup, NT_187677.1:g.147098_147100dup, NT_187677.1:g.147097_147100dup, NT_187677.1:g.147096_147100dup, NT_187677.1:g.147095_147100dup, NT_187677.1:g.147094_147100dup, NT_187677.1:g.147093_147100dup, NT_187677.1:g.147092_147100dup, NT_187677.1:g.147091_147100dup, NT_187677.1:g.147084_147100dup, NT_187677.1:g.147100_147101insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_016107311.1:g.90844_90857del, NW_016107311.1:g.90845_90857del, NW_016107311.1:g.90847_90857del, NW_016107311.1:g.90848_90857del, NW_016107311.1:g.90850_90857del, NW_016107311.1:g.90851_90857del, NW_016107311.1:g.90852_90857del, NW_016107311.1:g.90853_90857del, NW_016107311.1:g.90854_90857del, NW_016107311.1:g.90855_90857del, NW_016107311.1:g.90856_90857del, NW_016107311.1:g.90857del, NW_016107311.1:g.90857dup, NW_016107311.1:g.90856_90857dup, NW_016107311.1:g.90855_90857dup, NW_016107311.1:g.90854_90857dup, NW_016107311.1:g.90853_90857dup, NW_016107311.1:g.90852_90857dup, NW_016107311.1:g.90851_90857dup, NW_016107311.1:g.90850_90857dup, NW_016107311.1:g.90849_90857dup, NW_016107311.1:g.90848_90857dup, NW_016107311.1:g.90841_90857dup, NW_016107311.1:g.90857_90858insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_016107308.1:g.92117_92118dup, NW_016107308.1:g.92107_92118del, NW_016107308.1:g.92108_92118del, NW_016107308.1:g.92110_92118del, NW_016107308.1:g.92111_92118del, NW_016107308.1:g.92113_92118del, NW_016107308.1:g.92114_92118del, NW_016107308.1:g.92115_92118del, NW_016107308.1:g.92116_92118del, NW_016107308.1:g.92117_92118del, NW_016107308.1:g.92118del, NW_016107308.1:g.92118dup, NW_016107308.1:g.92116_92118dup, NW_016107308.1:g.92115_92118dup, NW_016107308.1:g.92114_92118dup, NW_016107308.1:g.92113_92118dup, NW_016107308.1:g.92112_92118dup, NW_016107308.1:g.92111_92118dup, NW_016107308.1:g.92110_92118dup, NW_016107308.1:g.92109_92118dup, NW_016107308.1:g.92108_92118dup, NW_016107308.1:g.92107_92118dup, NW_016107308.1:g.92100_92118dup, NW_016107308.1:g.92118_92119insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_016107312.1:g.42261_42274del, NW_016107312.1:g.42262_42274del, NW_016107312.1:g.42264_42274del, NW_016107312.1:g.42265_42274del, NW_016107312.1:g.42267_42274del, NW_016107312.1:g.42268_42274del, NW_016107312.1:g.42269_42274del, NW_016107312.1:g.42270_42274del, NW_016107312.1:g.42271_42274del, NW_016107312.1:g.42272_42274del, NW_016107312.1:g.42273_42274del, NW_016107312.1:g.42274del, NW_016107312.1:g.42274dup, NW_016107312.1:g.42273_42274dup, NW_016107312.1:g.42272_42274dup, NW_016107312.1:g.42271_42274dup, NW_016107312.1:g.42270_42274dup, NW_016107312.1:g.42269_42274dup, NW_016107312.1:g.42268_42274dup, NW_016107312.1:g.42267_42274dup, NW_016107312.1:g.42266_42274dup, NW_016107312.1:g.42265_42274dup, NW_016107312.1:g.42258_42274dup, NW_016107312.1:g.42274_42275insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.1:g.514999_515000dup, NW_003571055.1:g.514989_515000del, NW_003571055.1:g.514990_515000del, NW_003571055.1:g.514992_515000del, NW_003571055.1:g.514993_515000del, NW_003571055.1:g.514995_515000del, NW_003571055.1:g.514996_515000del, NW_003571055.1:g.514997_515000del, NW_003571055.1:g.514998_515000del, NW_003571055.1:g.514999_515000del, NW_003571055.1:g.515000del, NW_003571055.1:g.515000dup, NW_003571055.1:g.514998_515000dup, NW_003571055.1:g.514997_515000dup, NW_003571055.1:g.514996_515000dup, NW_003571055.1:g.514995_515000dup, NW_003571055.1:g.514994_515000dup, NW_003571055.1:g.514993_515000dup, NW_003571055.1:g.514992_515000dup, NW_003571055.1:g.514991_515000dup, NW_003571055.1:g.514990_515000dup, NW_003571055.1:g.514989_515000dup, NW_003571055.1:g.514982_515000dup, NW_003571055.1:g.515000_515001insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_003571059.1:g.788316_788317dup, NW_003571059.1:g.788306_788317del, NW_003571059.1:g.788307_788317del, NW_003571059.1:g.788309_788317del, NW_003571059.1:g.788310_788317del, NW_003571059.1:g.788312_788317del, NW_003571059.1:g.788313_788317del, NW_003571059.1:g.788314_788317del, NW_003571059.1:g.788315_788317del, NW_003571059.1:g.788316_788317del, NW_003571059.1:g.788317del, NW_003571059.1:g.788317dup, NW_003571059.1:g.788315_788317dup, NW_003571059.1:g.788314_788317dup, NW_003571059.1:g.788313_788317dup, NW_003571059.1:g.788312_788317dup, NW_003571059.1:g.788311_788317dup, NW_003571059.1:g.788310_788317dup, NW_003571059.1:g.788309_788317dup, NW_003571059.1:g.788308_788317dup, NW_003571059.1:g.788307_788317dup, NW_003571059.1:g.788306_788317dup, NW_003571059.1:g.788299_788317dup, NW_003571059.1:g.788317_788318insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_003571058.1:g.851669dup, NW_003571058.1:g.851657_851669del, NW_003571058.1:g.851658_851669del, NW_003571058.1:g.851660_851669del, NW_003571058.1:g.851661_851669del, NW_003571058.1:g.851663_851669del, NW_003571058.1:g.851664_851669del, NW_003571058.1:g.851665_851669del, NW_003571058.1:g.851666_851669del, NW_003571058.1:g.851667_851669del, NW_003571058.1:g.851668_851669del, NW_003571058.1:g.851669del, NW_003571058.1:g.851668_851669dup, NW_003571058.1:g.851667_851669dup, NW_003571058.1:g.851666_851669dup, NW_003571058.1:g.851665_851669dup, NW_003571058.1:g.851664_851669dup, NW_003571058.1:g.851663_851669dup, NW_003571058.1:g.851662_851669dup, NW_003571058.1:g.851661_851669dup, NW_003571058.1:g.851660_851669dup, NW_003571058.1:g.851659_851669dup, NW_003571058.1:g.851652_851669dup, NW_003571058.1:g.851669_851670insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

                                        20.

                                        rs1491305539 [Homo sapiens]
                                          Variant type:
                                          DEL
                                          Alleles:
                                          AT>- [Show Flanks]
                                          Chromosome:
                                          19:54879676 (GRCh38)
                                          19:55391132 (GRCh37)
                                          Canonical SPDI:
                                          NC_000019.10:54879675:AT:
                                          Gene:
                                          FCAR (Varview)
                                          Functional Consequence:
                                          intron_variant,genic_upstream_transcript_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          -=0.00049/8 (ALFA)
                                          -=0.00024/21 (GnomAD)
                                          HGVS:

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