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Items: 1 to 20 of 2540

1.

rs1491586288 has merged into rs1021105171 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    GT>- [Show Flanks]
    Chromosome:
    15:22868624 (GRCh38)
    15:23004444 (GRCh37)
    Canonical SPDI:
    NC_000015.10:22868622:TGT:T
    Gene:
    CYFIP1 (Varview), NIPA2 (Varview)
    Functional Consequence:
    downstream_transcript_variant,3_prime_UTR_variant,500B_downstream_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0./0 (ALFA)
    -=0.000012/1 (GnomAD)
    -=0.000015/4 (TOPMED)
    HGVS:

    2.

    rs1491545835 has merged into rs552579436 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      AG>-,AGAG [Show Flanks]
      Chromosome:
      15:22867249 (GRCh38)
      15:23005820 (GRCh37)
      Canonical SPDI:
      NC_000015.10:22867246:AGAG:AG,NC_000015.10:22867246:AGAG:AGAGAG
      Gene:
      CYFIP1 (Varview), NIPA2 (Varview)
      Functional Consequence:
      3_prime_UTR_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      AGAGAG=0./0 (ALFA)
      -=0.001/1 (GoNL)
      CT=0.99994/16759 (TOMMO)
      HGVS:
      NC_000015.10:g.22867247AG[1], NC_000015.10:g.22867247AG[3], NC_000015.9:g.23005818CT[1], NC_000015.9:g.23005818CT[3], NG_054889.1:g.118657CT[1], NG_054889.1:g.118657CT[3], NM_014608.6:c.*2778CT[1], NM_014608.6:c.*2778CT[3], NM_014608.5:c.*2778CT[1], NM_014608.5:c.*2778CT[3], NM_001287810.4:c.*2778CT[1], NM_001287810.4:c.*2778CT[3], NM_001287810.3:c.*2778CT[1], NM_001287810.3:c.*2778CT[3], NM_001324122.3:c.*2778CT[1], NM_001324122.3:c.*2778CT[3], NM_001324122.2:c.*2778CT[1], NM_001324122.2:c.*2778CT[3], NM_001324123.3:c.*2778CT[1], NM_001324123.3:c.*2778CT[3], NM_001324123.2:c.*2778CT[1], NM_001324123.2:c.*2778CT[3], NM_001324124.3:c.*2778CT[1], NM_001324124.3:c.*2778CT[3], NM_001324124.2:c.*2778CT[1], NM_001324124.2:c.*2778CT[3], NM_001324126.3:c.*2778CT[1], NM_001324126.3:c.*2778CT[3], NM_001324126.2:c.*2778CT[1], NM_001324126.2:c.*2778CT[3], NM_001324125.3:c.*2778CT[1], NM_001324125.3:c.*2778CT[3], NM_001324125.2:c.*2778CT[1], NM_001324125.2:c.*2778CT[3], NM_001033028.3:c.*2778CT[1], NM_001033028.3:c.*2778CT[3], NM_001033028.2:c.*2778CT[1], NM_001033028.2:c.*2778CT[3], NM_001324120.2:c.*2778CT[1], NM_001324120.2:c.*2778CT[3], NM_001324119.2:c.*2778CT[1], NM_001324119.2:c.*2778CT[3], NG_021303.1:g.33607AG[1], NG_021303.1:g.33607AG[3], NM_030922.7:c.*400AG[1], NM_030922.7:c.*400AG[3], NM_030922.6:c.*400AG[1], NM_030922.6:c.*400AG[3], NM_001008860.3:c.*400AG[1], NM_001008860.3:c.*400AG[3], NM_001008860.2:c.*400AG[1], NM_001008860.2:c.*400AG[3], NM_001008892.3:c.*400AG[1], NM_001008892.3:c.*400AG[3], NM_001008892.2:c.*400AG[1], NM_001008892.2:c.*400AG[3], NM_001008894.3:c.*400AG[1], NM_001008894.3:c.*400AG[3], NM_001008894.2:c.*400AG[1], NM_001008894.2:c.*400AG[3], NM_001184889.2:c.*400AG[1], NM_001184889.2:c.*400AG[3], NM_001184889.1:c.*400AG[1], NM_001184889.1:c.*400AG[3], NM_001184888.2:c.*400AG[1], NM_001184888.2:c.*400AG[3], NM_001184888.1:c.*400AG[1], NM_001184888.1:c.*400AG[3], NW_021160017.1:g.3761322AG[1], NW_021160017.1:g.3761322AG[3], XM_005272548.4:c.*400AG[1], XM_005272548.4:c.*400AG[3], XM_005272548.3:c.*400AG[1], XM_005272548.3:c.*400AG[3], XM_005272548.2:c.*400AG[1], XM_005272548.2:c.*400AG[3], XM_005272548.1:c.*400AG[1], XM_005272548.1:c.*400AG[3], XM_005272553.6:c.*400AG[1], XM_005272553.6:c.*400AG[3], XM_005272553.5:c.*400AG[1], XM_005272553.5:c.*400AG[3], XM_005272553.4:c.*400AG[1], XM_005272553.4:c.*400AG[3], XM_005272553.3:c.*400AG[1], XM_005272553.3:c.*400AG[3], XM_005272553.2:c.*400AG[1], XM_005272553.2:c.*400AG[3], XM_005272553.1:c.*400AG[1], XM_005272553.1:c.*400AG[3], XM_011543878.4:c.*400AG[1], XM_011543878.4:c.*400AG[3], XM_011543878.3:c.*400AG[1], XM_011543878.3:c.*400AG[3], XM_011543878.2:c.*400AG[1], XM_011543878.2:c.*400AG[3], XM_011543878.1:c.*400AG[1], XM_011543878.1:c.*400AG[3], XM_005272546.4:c.*400AG[1], XM_005272546.4:c.*400AG[3], XM_005272546.3:c.*400AG[1], XM_005272546.3:c.*400AG[3], XM_005272546.2:c.*400AG[1], XM_005272546.2:c.*400AG[3], XM_005272546.1:c.*400AG[1], XM_005272546.1:c.*400AG[3], XM_005272547.5:c.*400AG[1], XM_005272547.5:c.*400AG[3], XM_005272547.4:c.*400AG[1], XM_005272547.4:c.*400AG[3], XM_005272547.3:c.*400AG[1], XM_005272547.3:c.*400AG[3], XM_005272547.2:c.*400AG[1], XM_005272547.2:c.*400AG[3], XM_005272547.1:c.*400AG[1], XM_005272547.1:c.*400AG[3], XM_005272552.5:c.*400AG[1], XM_005272552.5:c.*400AG[3], XM_005272552.4:c.*400AG[1], XM_005272552.4:c.*400AG[3], XM_005272552.3:c.*400AG[1], XM_005272552.3:c.*400AG[3], XM_005272552.2:c.*400AG[1], XM_005272552.2:c.*400AG[3], XM_005272552.1:c.*400AG[1], XM_005272552.1:c.*400AG[3], XM_011543880.4:c.*400AG[1], XM_011543880.4:c.*400AG[3], XM_011543880.3:c.*400AG[1], XM_011543880.3:c.*400AG[3], XM_011543880.2:c.*400AG[1], XM_011543880.2:c.*400AG[3], XM_011543880.1:c.*400AG[1], XM_011543880.1:c.*400AG[3], XM_005272550.4:c.*400AG[1], XM_005272550.4:c.*400AG[3], XM_005272550.3:c.*400AG[1], XM_005272550.3:c.*400AG[3], XM_005272550.2:c.*400AG[1], XM_005272550.2:c.*400AG[3], XM_005272550.1:c.*400AG[1], XM_005272550.1:c.*400AG[3], XM_011543879.4:c.*400AG[1], XM_011543879.4:c.*400AG[3], XM_011543879.3:c.*400AG[1], XM_011543879.3:c.*400AG[3], XM_011543879.2:c.*400AG[1], XM_011543879.2:c.*400AG[3], XM_011543879.1:c.*400AG[1], XM_011543879.1:c.*400AG[3], XM_017022651.3:c.*400AG[1], XM_017022651.3:c.*400AG[3], XM_017022651.2:c.*400AG[1], XM_017022651.2:c.*400AG[3], XM_017022651.1:c.*400AG[1], XM_017022651.1:c.*400AG[3], XM_017022653.3:c.*400AG[1], XM_017022653.3:c.*400AG[3], XM_017022653.2:c.*400AG[1], XM_017022653.2:c.*400AG[3], XM_017022653.1:c.*400AG[1], XM_017022653.1:c.*400AG[3], XM_011543877.3:c.*400AG[1], XM_011543877.3:c.*400AG[3], XM_011543877.2:c.*400AG[1], XM_011543877.2:c.*400AG[3], XM_011543877.1:c.*400AG[1], XM_011543877.1:c.*400AG[3], XM_017022649.3:c.*400AG[1], XM_017022649.3:c.*400AG[3], XM_017022649.2:c.*400AG[1], XM_017022649.2:c.*400AG[3], XM_017022649.1:c.*400AG[1], XM_017022649.1:c.*400AG[3], XM_017022650.3:c.*400AG[1], XM_017022650.3:c.*400AG[3], XM_017022650.2:c.*400AG[1], XM_017022650.2:c.*400AG[3], XM_017022650.1:c.*400AG[1], XM_017022650.1:c.*400AG[3], XM_006720364.3:c.*400AG[1], XM_006720364.3:c.*400AG[3], XM_006720364.2:c.*400AG[1], XM_006720364.2:c.*400AG[3], XM_006720364.1:c.*400AG[1], XM_006720364.1:c.*400AG[3], XM_017022652.3:c.*400AG[1], XM_017022652.3:c.*400AG[3], XM_017022652.2:c.*400AG[1], XM_017022652.2:c.*400AG[3], XM_017022652.1:c.*400AG[1], XM_017022652.1:c.*400AG[3], XM_017022654.3:c.*400AG[1], XM_017022654.3:c.*400AG[3], XM_017022654.2:c.*400AG[1], XM_017022654.2:c.*400AG[3], XM_017022654.1:c.*400AG[1], XM_017022654.1:c.*400AG[3], XM_017022645.2:c.*400AG[1], XM_017022645.2:c.*400AG[3], XM_017022645.1:c.*400AG[1], XM_017022645.1:c.*400AG[3], XM_017022646.2:c.*400AG[1], XM_017022646.2:c.*400AG[3], XM_017022646.1:c.*400AG[1], XM_017022646.1:c.*400AG[3], XM_017022647.2:c.*400AG[1], XM_017022647.2:c.*400AG[3], XM_017022647.1:c.*400AG[1], XM_017022647.1:c.*400AG[3], XM_017022660.2:c.*400AG[1], XM_017022660.2:c.*400AG[3], XM_017022660.1:c.*400AG[1], XM_017022660.1:c.*400AG[3], XM_017022657.2:c.*400AG[1], XM_017022657.2:c.*400AG[3], XM_017022657.1:c.*400AG[1], XM_017022657.1:c.*400AG[3], XM_017022659.2:c.*400AG[1], XM_017022659.2:c.*400AG[3], XM_017022659.1:c.*400AG[1], XM_017022659.1:c.*400AG[3], XM_017022656.2:c.*400AG[1], XM_017022656.2:c.*400AG[3], XM_017022656.1:c.*400AG[1], XM_017022656.1:c.*400AG[3], XM_017022655.2:c.*400AG[1], XM_017022655.2:c.*400AG[3], XM_017022655.1:c.*400AG[1], XM_017022655.1:c.*400AG[3], XM_017022662.2:c.*400AG[1], XM_017022662.2:c.*400AG[3], XM_017022662.1:c.*400AG[1], XM_017022662.1:c.*400AG[3], XM_017022661.2:c.*400AG[1], XM_017022661.2:c.*400AG[3], XM_017022661.1:c.*400AG[1], XM_017022661.1:c.*400AG[3], XM_017022658.2:c.*400AG[1], XM_017022658.2:c.*400AG[3], XM_017022658.1:c.*400AG[1], XM_017022658.1:c.*400AG[3], XM_017022663.2:c.*400AG[1], XM_017022663.2:c.*400AG[3], XM_017022663.1:c.*400AG[1], XM_017022663.1:c.*400AG[3], XM_017022648.2:c.*400AG[1], XM_017022648.2:c.*400AG[3], XM_017022648.1:c.*400AG[1], XM_017022648.1:c.*400AG[3], XM_006720367.2:c.*400AG[1], XM_006720367.2:c.*400AG[3], XM_006720367.1:c.*400AG[1], XM_006720367.1:c.*400AG[3], XM_047433156.1:c.*400AG[1], XM_047433156.1:c.*400AG[3], XM_047433150.1:c.*400AG[1], XM_047433150.1:c.*400AG[3], XM_047433155.1:c.*400AG[1], XM_047433155.1:c.*400AG[3], XM_047433158.1:c.*400AG[1], XM_047433158.1:c.*400AG[3], XM_047433151.1:c.*400AG[1], XM_047433151.1:c.*400AG[3], XM_047433162.1:c.*400AG[1], XM_047433162.1:c.*400AG[3], XM_047433154.1:c.*400AG[1], XM_047433154.1:c.*400AG[3], XM_047433157.1:c.*400AG[1], XM_047433157.1:c.*400AG[3], XM_047433153.1:c.*400AG[1], XM_047433153.1:c.*400AG[3], XM_047433163.1:c.*400AG[1], XM_047433163.1:c.*400AG[3], XM_047433152.1:c.*400AG[1], XM_047433152.1:c.*400AG[3], XM_047433161.1:c.*400AG[1], XM_047433161.1:c.*400AG[3], XM_047433159.1:c.*400AG[1], XM_047433159.1:c.*400AG[3], XM_047433160.1:c.*400AG[1], XM_047433160.1:c.*400AG[3]

      3.

      rs1491484686 [Homo sapiens]
        Variant type:
        INS
        Alleles:
        ->C [Show Flanks]
        Chromosome:
        15:22868469 (GRCh38)
        15:23004599 (GRCh37)
        Canonical SPDI:
        NC_000015.10:22868469::C
        Gene:
        CYFIP1 (Varview), NIPA2 (Varview)
        Functional Consequence:
        3_prime_UTR_variant,downstream_transcript_variant,500B_downstream_variant
        Validated:
        by frequency,by alfa
        MAF:
        C=0.0004/2 (ALFA)
        G=0.0004/2 (Estonian)
        HGVS:

        4.

        rs1491451586 [Homo sapiens]
          Variant type:
          DEL
          Alleles:
          CA>- [Show Flanks]
          Chromosome:
          15:22867541 (GRCh38)
          15:23005526 (GRCh37)
          Canonical SPDI:
          NC_000015.10:22867540:CA:
          Gene:
          CYFIP1 (Varview), NIPA2 (Varview)
          Functional Consequence:
          3_prime_UTR_variant
          Validated:
          by frequency
          MAF:
          -=0.000007/1 (GnomAD)
          HGVS:
          NC_000015.10:g.22867541_22867542del, NC_000015.9:g.23005526_23005527del, NG_054889.1:g.118365_118366del, NM_014608.6:c.*2486_*2487del, NM_014608.5:c.*2486_*2487del, NM_001287810.4:c.*2486_*2487del, NM_001287810.3:c.*2486_*2487del, NM_001324122.3:c.*2486_*2487del, NM_001324122.2:c.*2486_*2487del, NM_001324123.3:c.*2486_*2487del, NM_001324123.2:c.*2486_*2487del, NM_001324124.3:c.*2486_*2487del, NM_001324124.2:c.*2486_*2487del, NM_001324126.3:c.*2486_*2487del, NM_001324126.2:c.*2486_*2487del, NM_001324125.3:c.*2486_*2487del, NM_001324125.2:c.*2486_*2487del, NM_001033028.3:c.*2486_*2487del, NM_001033028.2:c.*2486_*2487del, NM_001324120.2:c.*2486_*2487del, NM_001324119.2:c.*2486_*2487del, NG_021303.1:g.33901_33902del, NM_030922.7:c.*694_*695del, NM_030922.6:c.*694_*695del, NM_001008860.3:c.*694_*695del, NM_001008860.2:c.*694_*695del, NM_001008892.3:c.*694_*695del, NM_001008892.2:c.*694_*695del, NM_001008894.3:c.*694_*695del, NM_001008894.2:c.*694_*695del, NM_001184889.2:c.*694_*695del, NM_001184889.1:c.*694_*695del, NM_001184888.2:c.*694_*695del, NM_001184888.1:c.*694_*695del, NW_021160017.1:g.3761616_3761617del, XM_005272548.4:c.*694_*695del, XM_005272548.3:c.*694_*695del, XM_005272548.2:c.*694_*695del, XM_005272548.1:c.*694_*695del, XM_005272553.6:c.*694_*695del, XM_005272553.5:c.*694_*695del, XM_005272553.4:c.*694_*695del, XM_005272553.3:c.*694_*695del, XM_005272553.2:c.*694_*695del, XM_005272553.1:c.*694_*695del, XM_011543878.4:c.*694_*695del, XM_011543878.3:c.*694_*695del, XM_011543878.2:c.*694_*695del, XM_011543878.1:c.*694_*695del, XM_005272546.4:c.*694_*695del, XM_005272546.3:c.*694_*695del, XM_005272546.2:c.*694_*695del, XM_005272546.1:c.*694_*695del, XM_005272547.5:c.*694_*695del, XM_005272547.4:c.*694_*695del, XM_005272547.3:c.*694_*695del, XM_005272547.2:c.*694_*695del, XM_005272547.1:c.*694_*695del, XM_005272552.5:c.*694_*695del, XM_005272552.4:c.*694_*695del, XM_005272552.3:c.*694_*695del, XM_005272552.2:c.*694_*695del, XM_005272552.1:c.*694_*695del, XM_011543880.4:c.*694_*695del, XM_011543880.3:c.*694_*695del, XM_011543880.2:c.*694_*695del, XM_011543880.1:c.*694_*695del, XM_005272550.4:c.*694_*695del, XM_005272550.3:c.*694_*695del, XM_005272550.2:c.*694_*695del, XM_005272550.1:c.*694_*695del, XM_011543879.4:c.*694_*695del, XM_011543879.3:c.*694_*695del, XM_011543879.2:c.*694_*695del, XM_011543879.1:c.*694_*695del, XM_017022651.3:c.*694_*695del, XM_017022651.2:c.*694_*695del, XM_017022651.1:c.*694_*695del, XM_017022653.3:c.*694_*695del, XM_017022653.2:c.*694_*695del, XM_017022653.1:c.*694_*695del, XM_011543877.3:c.*694_*695del, XM_011543877.2:c.*694_*695del, XM_011543877.1:c.*694_*695del, XM_017022649.3:c.*694_*695del, XM_017022649.2:c.*694_*695del, XM_017022649.1:c.*694_*695del, XM_017022650.3:c.*694_*695del, XM_017022650.2:c.*694_*695del, XM_017022650.1:c.*694_*695del, XM_006720364.3:c.*694_*695del, XM_006720364.2:c.*694_*695del, XM_006720364.1:c.*694_*695del, XM_017022652.3:c.*694_*695del, XM_017022652.2:c.*694_*695del, XM_017022652.1:c.*694_*695del, XM_017022654.3:c.*694_*695del, XM_017022654.2:c.*694_*695del, XM_017022654.1:c.*694_*695del, XM_017022645.2:c.*694_*695del, XM_017022645.1:c.*694_*695del, XM_017022648.2:c.*694_*695del, XM_017022648.1:c.*694_*695del, XM_006720367.2:c.*694_*695del, XM_006720367.1:c.*694_*695del, XM_017022646.2:c.*694_*695del, XM_017022646.1:c.*694_*695del, XM_017022647.2:c.*694_*695del, XM_017022647.1:c.*694_*695del, XM_017022660.2:c.*694_*695del, XM_017022660.1:c.*694_*695del, XM_017022657.2:c.*694_*695del, XM_017022657.1:c.*694_*695del, XM_017022659.2:c.*694_*695del, XM_017022659.1:c.*694_*695del, XM_017022655.2:c.*694_*695del, XM_017022655.1:c.*694_*695del, XM_017022662.2:c.*694_*695del, XM_017022662.1:c.*694_*695del, XM_017022661.2:c.*694_*695del, XM_017022661.1:c.*694_*695del, XM_017022658.2:c.*694_*695del, XM_017022658.1:c.*694_*695del, XM_017022663.2:c.*694_*695del, XM_017022663.1:c.*694_*695del, XM_047433159.1:c.*694_*695del, XM_017022656.2:c.*694_*695del, XM_017022656.1:c.*694_*695del, XM_047433152.1:c.*694_*695del, XM_047433162.1:c.*694_*695del, XM_047433154.1:c.*694_*695del, XM_047433153.1:c.*694_*695del, XM_047433161.1:c.*694_*695del, XM_047433158.1:c.*694_*695del, XM_047433156.1:c.*694_*695del, XM_047433151.1:c.*694_*695del, XM_047433160.1:c.*694_*695del, XM_047433163.1:c.*694_*695del, XM_047433155.1:c.*694_*695del, XM_047433157.1:c.*694_*695del, XM_047433150.1:c.*694_*695del

          5.

          rs1491399347 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            TA>- [Show Flanks]
            Chromosome:
            15:22867953 (GRCh38)
            15:23005115 (GRCh37)
            Canonical SPDI:
            NC_000015.10:22867951:ATA:A
            Gene:
            CYFIP1 (Varview), NIPA2 (Varview)
            Functional Consequence:
            3_prime_UTR_variant
            Validated:
            by frequency,by alfa
            MAF:
            A=0./0 (ALFA)
            -=0.000008/2 (TOPMED)
            HGVS:
            NC_000015.10:g.22867953_22867954del, NC_000015.9:g.23005115_23005116del, NG_054889.1:g.117954_117955del, NM_014608.6:c.*2075_*2076del, NM_014608.5:c.*2075_*2076del, NM_001287810.4:c.*2075_*2076del, NM_001287810.3:c.*2075_*2076del, NM_001324122.3:c.*2075_*2076del, NM_001324122.2:c.*2075_*2076del, NM_001324123.3:c.*2075_*2076del, NM_001324123.2:c.*2075_*2076del, NM_001324124.3:c.*2075_*2076del, NM_001324124.2:c.*2075_*2076del, NM_001324126.3:c.*2075_*2076del, NM_001324126.2:c.*2075_*2076del, NM_001324125.3:c.*2075_*2076del, NM_001324125.2:c.*2075_*2076del, NM_001033028.3:c.*2075_*2076del, NM_001033028.2:c.*2075_*2076del, NM_001324120.2:c.*2075_*2076del, NM_001324119.2:c.*2075_*2076del, NG_021303.1:g.34313_34314del, NM_030922.7:c.*1106_*1107del, NM_030922.6:c.*1106_*1107del, NM_001008860.3:c.*1106_*1107del, NM_001008860.2:c.*1106_*1107del, NM_001008892.3:c.*1106_*1107del, NM_001008892.2:c.*1106_*1107del, NM_001008894.3:c.*1106_*1107del, NM_001008894.2:c.*1106_*1107del, NM_001184889.2:c.*1106_*1107del, NM_001184889.1:c.*1106_*1107del, NM_001184888.2:c.*1106_*1107del, NM_001184888.1:c.*1106_*1107del, NW_021160017.1:g.3762033_3762034del, XM_005272548.4:c.*1106_*1107del, XM_005272548.3:c.*1106_*1107del, XM_005272548.2:c.*1106_*1107del, XM_005272548.1:c.*1106_*1107del, XM_005272553.6:c.*1106_*1107del, XM_005272553.5:c.*1106_*1107del, XM_005272553.4:c.*1106_*1107del, XM_005272553.3:c.*1106_*1107del, XM_005272553.2:c.*1106_*1107del, XM_005272553.1:c.*1106_*1107del, XM_011543878.4:c.*1106_*1107del, XM_011543878.3:c.*1106_*1107del, XM_011543878.2:c.*1106_*1107del, XM_011543878.1:c.*1106_*1107del, XM_005272546.4:c.*1106_*1107del, XM_005272546.3:c.*1106_*1107del, XM_005272546.2:c.*1106_*1107del, XM_005272546.1:c.*1106_*1107del, XM_005272547.5:c.*1106_*1107del, XM_005272547.4:c.*1106_*1107del, XM_005272547.3:c.*1106_*1107del, XM_005272547.2:c.*1106_*1107del, XM_005272547.1:c.*1106_*1107del, XM_005272552.5:c.*1106_*1107del, XM_005272552.4:c.*1106_*1107del, XM_005272552.3:c.*1106_*1107del, XM_005272552.2:c.*1106_*1107del, XM_005272552.1:c.*1106_*1107del, XM_011543880.4:c.*1106_*1107del, XM_011543880.3:c.*1106_*1107del, XM_011543880.2:c.*1106_*1107del, XM_011543880.1:c.*1106_*1107del, XM_005272550.4:c.*1106_*1107del, XM_005272550.3:c.*1106_*1107del, XM_005272550.2:c.*1106_*1107del, XM_005272550.1:c.*1106_*1107del, XM_011543879.4:c.*1106_*1107del, XM_011543879.3:c.*1106_*1107del, XM_011543879.2:c.*1106_*1107del, XM_011543879.1:c.*1106_*1107del, XM_017022651.3:c.*1106_*1107del, XM_017022651.2:c.*1106_*1107del, XM_017022651.1:c.*1106_*1107del, XM_017022653.3:c.*1106_*1107del, XM_017022653.2:c.*1106_*1107del, XM_017022653.1:c.*1106_*1107del, XM_011543877.3:c.*1106_*1107del, XM_011543877.2:c.*1106_*1107del, XM_011543877.1:c.*1106_*1107del, XM_017022649.3:c.*1106_*1107del, XM_017022649.2:c.*1106_*1107del, XM_017022649.1:c.*1106_*1107del, XM_017022650.3:c.*1106_*1107del, XM_017022650.2:c.*1106_*1107del, XM_017022650.1:c.*1106_*1107del, XM_006720364.3:c.*1106_*1107del, XM_006720364.2:c.*1106_*1107del, XM_006720364.1:c.*1106_*1107del, XM_017022652.3:c.*1106_*1107del, XM_017022652.2:c.*1106_*1107del, XM_017022652.1:c.*1106_*1107del, XM_017022654.3:c.*1106_*1107del, XM_017022654.2:c.*1106_*1107del, XM_017022654.1:c.*1106_*1107del, XM_017022645.2:c.*1106_*1107del, XM_017022645.1:c.*1106_*1107del, XM_017022648.2:c.*1106_*1107del, XM_017022648.1:c.*1106_*1107del, XM_006720367.2:c.*1106_*1107del, XM_006720367.1:c.*1106_*1107del, XM_017022646.2:c.*1106_*1107del, XM_017022646.1:c.*1106_*1107del, XM_017022647.2:c.*1106_*1107del, XM_017022647.1:c.*1106_*1107del, XM_017022660.2:c.*1106_*1107del, XM_017022660.1:c.*1106_*1107del, XM_017022657.2:c.*1106_*1107del, XM_017022657.1:c.*1106_*1107del, XM_017022659.2:c.*1106_*1107del, XM_017022659.1:c.*1106_*1107del, XM_017022655.2:c.*1106_*1107del, XM_017022655.1:c.*1106_*1107del, XM_017022662.2:c.*1106_*1107del, XM_017022662.1:c.*1106_*1107del, XM_017022661.2:c.*1106_*1107del, XM_017022661.1:c.*1106_*1107del, XM_017022658.2:c.*1106_*1107del, XM_017022658.1:c.*1106_*1107del, XM_017022663.2:c.*1106_*1107del, XM_017022663.1:c.*1106_*1107del, XM_047433156.1:c.*1106_*1107del, XM_047433150.1:c.*1106_*1107del, XM_047433151.1:c.*1106_*1107del, XM_047433159.1:c.*1106_*1107del, XM_047433160.1:c.*1106_*1107del, XM_047433153.1:c.*1106_*1107del, XM_047433161.1:c.*1106_*1107del, XM_047433157.1:c.*1106_*1107del, XM_047433152.1:c.*1106_*1107del, XM_047433162.1:c.*1106_*1107del, XM_047433158.1:c.*1106_*1107del, XM_017022656.2:c.*1106_*1107del, XM_017022656.1:c.*1106_*1107del, XM_047433163.1:c.*1106_*1107del, XM_047433155.1:c.*1106_*1107del, XM_047433154.1:c.*1106_*1107del

            6.

            rs1491276244 has merged into rs1394515053 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              ->TGTTT [Show Flanks]
              Chromosome:
              15:22868617 (GRCh38)
              15:23004445 (GRCh37)
              Canonical SPDI:
              NC_000015.10:22868617:TTGTTT:TTGTTTTGTTT
              Gene:
              CYFIP1 (Varview), NIPA2 (Varview)
              Functional Consequence:
              3_prime_UTR_variant,500B_downstream_variant,downstream_transcript_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              TTGTTTTGTTT=0./0 (ALFA)
              TTGTT=0.000007/1 (GnomAD)
              TTGTT=0.000019/5 (TOPMED)
              HGVS:

              7.

              rs1491225086 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                ->CTCA [Show Flanks]
                Chromosome:
                15:22868335 (GRCh38)
                15:23004728 (GRCh37)
                Canonical SPDI:
                NC_000015.10:22868335:ACTCA:ACTCACTCA
                Gene:
                CYFIP1 (Varview), NIPA2 (Varview)
                Functional Consequence:
                3_prime_UTR_variant
                Validated:
                by frequency,by alfa
                MAF:
                ACTCACTCA=0./0 (ALFA)
                ACTC=0.000004/1 (TOPMED)
                HGVS:
                NC_000015.10:g.22868337_22868340dup, NC_000015.9:g.23004729_23004732dup, NG_054889.1:g.117568_117571dup, NM_014608.6:c.*1689_*1692dup, NM_014608.5:c.*1689_*1692dup, NM_001287810.4:c.*1689_*1692dup, NM_001287810.3:c.*1689_*1692dup, NM_001324122.3:c.*1689_*1692dup, NM_001324122.2:c.*1689_*1692dup, NM_001324123.3:c.*1689_*1692dup, NM_001324123.2:c.*1689_*1692dup, NM_001324124.3:c.*1689_*1692dup, NM_001324124.2:c.*1689_*1692dup, NM_001324126.3:c.*1689_*1692dup, NM_001324126.2:c.*1689_*1692dup, NM_001324125.3:c.*1689_*1692dup, NM_001324125.2:c.*1689_*1692dup, NM_001033028.3:c.*1689_*1692dup, NM_001033028.2:c.*1689_*1692dup, NM_001324120.2:c.*1689_*1692dup, NM_001324119.2:c.*1689_*1692dup, NG_021303.1:g.34697_34700dup, NM_030922.7:c.*1490_*1493dup, NM_030922.6:c.*1490_*1493dup, NM_001008860.3:c.*1490_*1493dup, NM_001008860.2:c.*1490_*1493dup, NM_001008892.3:c.*1490_*1493dup, NM_001008892.2:c.*1490_*1493dup, NM_001008894.3:c.*1490_*1493dup, NM_001008894.2:c.*1490_*1493dup, NM_001184889.2:c.*1490_*1493dup, NM_001184889.1:c.*1490_*1493dup, NM_001184888.2:c.*1490_*1493dup, NM_001184888.1:c.*1490_*1493dup, NW_021160017.1:g.3762417_3762420dup, XM_005272548.4:c.*1490_*1493dup, XM_005272548.3:c.*1490_*1493dup, XM_005272548.2:c.*1490_*1493dup, XM_005272548.1:c.*1490_*1493dup, XM_005272553.6:c.*1490_*1493dup, XM_005272553.5:c.*1490_*1493dup, XM_005272553.4:c.*1490_*1493dup, XM_005272553.3:c.*1490_*1493dup, XM_005272553.2:c.*1490_*1493dup, XM_005272553.1:c.*1490_*1493dup, XM_011543878.4:c.*1490_*1493dup, XM_011543878.3:c.*1490_*1493dup, XM_011543878.2:c.*1490_*1493dup, XM_011543878.1:c.*1490_*1493dup, XM_005272546.4:c.*1490_*1493dup, XM_005272546.3:c.*1490_*1493dup, XM_005272546.2:c.*1490_*1493dup, XM_005272546.1:c.*1490_*1493dup, XM_005272547.5:c.*1490_*1493dup, XM_005272547.4:c.*1490_*1493dup, XM_005272547.3:c.*1490_*1493dup, XM_005272547.2:c.*1490_*1493dup, XM_005272547.1:c.*1490_*1493dup, XM_005272552.5:c.*1490_*1493dup, XM_005272552.4:c.*1490_*1493dup, XM_005272552.3:c.*1490_*1493dup, XM_005272552.2:c.*1490_*1493dup, XM_005272552.1:c.*1490_*1493dup, XM_011543880.4:c.*1490_*1493dup, XM_011543880.3:c.*1490_*1493dup, XM_011543880.2:c.*1490_*1493dup, XM_011543880.1:c.*1490_*1493dup, XM_005272550.4:c.*1490_*1493dup, XM_005272550.3:c.*1490_*1493dup, XM_005272550.2:c.*1490_*1493dup, XM_005272550.1:c.*1490_*1493dup, XM_011543879.4:c.*1490_*1493dup, XM_011543879.3:c.*1490_*1493dup, XM_011543879.2:c.*1490_*1493dup, XM_011543879.1:c.*1490_*1493dup, XM_017022651.3:c.*1490_*1493dup, XM_017022651.2:c.*1490_*1493dup, XM_017022651.1:c.*1490_*1493dup, XM_017022653.3:c.*1490_*1493dup, XM_017022653.2:c.*1490_*1493dup, XM_017022653.1:c.*1490_*1493dup, XM_011543877.3:c.*1490_*1493dup, XM_011543877.2:c.*1490_*1493dup, XM_011543877.1:c.*1490_*1493dup, XM_017022649.3:c.*1490_*1493dup, XM_017022649.2:c.*1490_*1493dup, XM_017022649.1:c.*1490_*1493dup, XM_017022650.3:c.*1490_*1493dup, XM_017022650.2:c.*1490_*1493dup, XM_017022650.1:c.*1490_*1493dup, XM_006720364.3:c.*1490_*1493dup, XM_006720364.2:c.*1490_*1493dup, XM_006720364.1:c.*1490_*1493dup, XM_017022652.3:c.*1490_*1493dup, XM_017022652.2:c.*1490_*1493dup, XM_017022652.1:c.*1490_*1493dup, XM_017022654.3:c.*1490_*1493dup, XM_017022654.2:c.*1490_*1493dup, XM_017022654.1:c.*1490_*1493dup, XM_017022645.2:c.*1490_*1493dup, XM_017022645.1:c.*1490_*1493dup, XM_017022648.2:c.*1490_*1493dup, XM_017022648.1:c.*1490_*1493dup, XM_006720367.2:c.*1490_*1493dup, XM_006720367.1:c.*1490_*1493dup, XM_017022646.2:c.*1490_*1493dup, XM_017022646.1:c.*1490_*1493dup, XM_017022647.2:c.*1490_*1493dup, XM_017022647.1:c.*1490_*1493dup, XM_017022660.2:c.*1490_*1493dup, XM_017022660.1:c.*1490_*1493dup, XM_017022657.2:c.*1490_*1493dup, XM_017022657.1:c.*1490_*1493dup, XM_017022659.2:c.*1490_*1493dup, XM_017022659.1:c.*1490_*1493dup, XM_017022655.2:c.*1490_*1493dup, XM_017022655.1:c.*1490_*1493dup, XM_017022662.2:c.*1490_*1493dup, XM_017022662.1:c.*1490_*1493dup, XM_017022661.2:c.*1490_*1493dup, XM_017022661.1:c.*1490_*1493dup, XM_017022658.2:c.*1490_*1493dup, XM_017022658.1:c.*1490_*1493dup, XM_017022663.2:c.*1490_*1493dup, XM_017022663.1:c.*1490_*1493dup, XM_047433156.1:c.*1490_*1493dup, XM_047433150.1:c.*1490_*1493dup, XM_047433151.1:c.*1490_*1493dup, XM_047433159.1:c.*1490_*1493dup, XM_047433160.1:c.*1490_*1493dup, XM_047433153.1:c.*1490_*1493dup, XM_047433161.1:c.*1490_*1493dup, XM_047433157.1:c.*1490_*1493dup, XM_047433152.1:c.*1490_*1493dup, XM_047433162.1:c.*1490_*1493dup, XM_047433158.1:c.*1490_*1493dup, XM_017022656.2:c.*1490_*1493dup, XM_017022656.1:c.*1490_*1493dup, XM_047433163.1:c.*1490_*1493dup, XM_047433155.1:c.*1490_*1493dup, XM_047433154.1:c.*1490_*1493dup

                8.

                rs1491159328 has merged into rs1422384277 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  GAGA>-,GA,GAGAGAGA [Show Flanks]
                  Chromosome:
                  15:22868333 (GRCh38)
                  15:23004733 (GRCh37)
                  Canonical SPDI:
                  NC_000015.10:22868331:AGAGA:A,NC_000015.10:22868331:AGAGA:AGA,NC_000015.10:22868331:AGAGA:AGAGAGAGA
                  Gene:
                  CYFIP1 (Varview), NIPA2 (Varview)
                  Functional Consequence:
                  3_prime_UTR_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  AGA=0./0 (ALFA)
                  HGVS:
                  NC_000015.10:g.22868333_22868336del, NC_000015.10:g.22868333GA[1], NC_000015.10:g.22868333GA[4], NC_000015.9:g.23004733_23004736del, NC_000015.9:g.23004733CT[1], NC_000015.9:g.23004733CT[4], NG_054889.1:g.117572_117575del, NG_054889.1:g.117572CT[1], NG_054889.1:g.117572CT[4], NM_014608.6:c.*1693_*1696del, NM_014608.6:c.*1693CT[1], NM_014608.6:c.*1693CT[4], NM_014608.5:c.*1693_*1696del, NM_014608.5:c.*1693CT[1], NM_014608.5:c.*1693CT[4], NM_001287810.4:c.*1693_*1696del, NM_001287810.4:c.*1693CT[1], NM_001287810.4:c.*1693CT[4], NM_001287810.3:c.*1693_*1696del, NM_001287810.3:c.*1693CT[1], NM_001287810.3:c.*1693CT[4], NM_001324122.3:c.*1693_*1696del, NM_001324122.3:c.*1693CT[1], NM_001324122.3:c.*1693CT[4], NM_001324122.2:c.*1693_*1696del, NM_001324122.2:c.*1693CT[1], NM_001324122.2:c.*1693CT[4], NM_001324123.3:c.*1693_*1696del, NM_001324123.3:c.*1693CT[1], NM_001324123.3:c.*1693CT[4], NM_001324123.2:c.*1693_*1696del, NM_001324123.2:c.*1693CT[1], NM_001324123.2:c.*1693CT[4], NM_001324124.3:c.*1693_*1696del, NM_001324124.3:c.*1693CT[1], NM_001324124.3:c.*1693CT[4], NM_001324124.2:c.*1693_*1696del, NM_001324124.2:c.*1693CT[1], NM_001324124.2:c.*1693CT[4], NM_001324126.3:c.*1693_*1696del, NM_001324126.3:c.*1693CT[1], NM_001324126.3:c.*1693CT[4], NM_001324126.2:c.*1693_*1696del, NM_001324126.2:c.*1693CT[1], NM_001324126.2:c.*1693CT[4], NM_001324125.3:c.*1693_*1696del, NM_001324125.3:c.*1693CT[1], NM_001324125.3:c.*1693CT[4], NM_001324125.2:c.*1693_*1696del, NM_001324125.2:c.*1693CT[1], NM_001324125.2:c.*1693CT[4], NM_001033028.3:c.*1693_*1696del, NM_001033028.3:c.*1693CT[1], NM_001033028.3:c.*1693CT[4], NM_001033028.2:c.*1693_*1696del, NM_001033028.2:c.*1693CT[1], NM_001033028.2:c.*1693CT[4], NM_001324120.2:c.*1693_*1696del, NM_001324120.2:c.*1693CT[1], NM_001324120.2:c.*1693CT[4], NM_001324119.2:c.*1693_*1696del, NM_001324119.2:c.*1693CT[1], NM_001324119.2:c.*1693CT[4], NG_021303.1:g.34693_34696del, NG_021303.1:g.34693GA[1], NG_021303.1:g.34693GA[4], NM_030922.7:c.*1486_*1489del, NM_030922.7:c.*1486GA[1], NM_030922.7:c.*1486GA[4], NM_030922.6:c.*1486_*1489del, NM_030922.6:c.*1486GA[1], NM_030922.6:c.*1486GA[4], NM_001008860.3:c.*1486_*1489del, NM_001008860.3:c.*1486GA[1], NM_001008860.3:c.*1486GA[4], NM_001008860.2:c.*1486_*1489del, NM_001008860.2:c.*1486GA[1], NM_001008860.2:c.*1486GA[4], NM_001008892.3:c.*1486_*1489del, NM_001008892.3:c.*1486GA[1], NM_001008892.3:c.*1486GA[4], NM_001008892.2:c.*1486_*1489del, NM_001008892.2:c.*1486GA[1], NM_001008892.2:c.*1486GA[4], NM_001008894.3:c.*1486_*1489del, NM_001008894.3:c.*1486GA[1], NM_001008894.3:c.*1486GA[4], NM_001008894.2:c.*1486_*1489del, NM_001008894.2:c.*1486GA[1], NM_001008894.2:c.*1486GA[4], NM_001184889.2:c.*1486_*1489del, NM_001184889.2:c.*1486GA[1], NM_001184889.2:c.*1486GA[4], NM_001184889.1:c.*1486_*1489del, NM_001184889.1:c.*1486GA[1], NM_001184889.1:c.*1486GA[4], NM_001184888.2:c.*1486_*1489del, NM_001184888.2:c.*1486GA[1], NM_001184888.2:c.*1486GA[4], NM_001184888.1:c.*1486_*1489del, NM_001184888.1:c.*1486GA[1], NM_001184888.1:c.*1486GA[4], NW_021160017.1:g.3762413_3762416del, NW_021160017.1:g.3762413GA[1], NW_021160017.1:g.3762413GA[4], XM_005272548.4:c.*1486_*1489del, XM_005272548.4:c.*1486GA[1], XM_005272548.4:c.*1486GA[4], XM_005272548.3:c.*1486_*1489del, XM_005272548.3:c.*1486GA[1], XM_005272548.3:c.*1486GA[4], XM_005272548.2:c.*1486_*1489del, XM_005272548.2:c.*1486GA[1], XM_005272548.2:c.*1486GA[4], XM_005272548.1:c.*1486_*1489del, XM_005272548.1:c.*1486GA[1], XM_005272548.1:c.*1486GA[4], XM_005272553.6:c.*1486_*1489del, XM_005272553.6:c.*1486GA[1], XM_005272553.6:c.*1486GA[4], XM_005272553.5:c.*1486_*1489del, XM_005272553.5:c.*1486GA[1], XM_005272553.5:c.*1486GA[4], XM_005272553.4:c.*1486_*1489del, XM_005272553.4:c.*1486GA[1], XM_005272553.4:c.*1486GA[4], XM_005272553.3:c.*1486_*1489del, XM_005272553.3:c.*1486GA[1], XM_005272553.3:c.*1486GA[4], XM_005272553.2:c.*1486_*1489del, XM_005272553.2:c.*1486GA[1], XM_005272553.2:c.*1486GA[4], XM_005272553.1:c.*1486_*1489del, XM_005272553.1:c.*1486GA[1], XM_005272553.1:c.*1486GA[4], XM_011543878.4:c.*1486_*1489del, XM_011543878.4:c.*1486GA[1], XM_011543878.4:c.*1486GA[4], XM_011543878.3:c.*1486_*1489del, XM_011543878.3:c.*1486GA[1], XM_011543878.3:c.*1486GA[4], XM_011543878.2:c.*1486_*1489del, XM_011543878.2:c.*1486GA[1], XM_011543878.2:c.*1486GA[4], XM_011543878.1:c.*1486_*1489del, XM_011543878.1:c.*1486GA[1], XM_011543878.1:c.*1486GA[4], XM_005272546.4:c.*1486_*1489del, XM_005272546.4:c.*1486GA[1], XM_005272546.4:c.*1486GA[4], XM_005272546.3:c.*1486_*1489del, XM_005272546.3:c.*1486GA[1], XM_005272546.3:c.*1486GA[4], XM_005272546.2:c.*1486_*1489del, XM_005272546.2:c.*1486GA[1], XM_005272546.2:c.*1486GA[4], XM_005272546.1:c.*1486_*1489del, XM_005272546.1:c.*1486GA[1], XM_005272546.1:c.*1486GA[4], XM_005272547.5:c.*1486_*1489del, XM_005272547.5:c.*1486GA[1], XM_005272547.5:c.*1486GA[4], XM_005272547.4:c.*1486_*1489del, XM_005272547.4:c.*1486GA[1], XM_005272547.4:c.*1486GA[4], XM_005272547.3:c.*1486_*1489del, XM_005272547.3:c.*1486GA[1], XM_005272547.3:c.*1486GA[4], XM_005272547.2:c.*1486_*1489del, XM_005272547.2:c.*1486GA[1], XM_005272547.2:c.*1486GA[4], XM_005272547.1:c.*1486_*1489del, XM_005272547.1:c.*1486GA[1], XM_005272547.1:c.*1486GA[4], XM_005272552.5:c.*1486_*1489del, XM_005272552.5:c.*1486GA[1], XM_005272552.5:c.*1486GA[4], XM_005272552.4:c.*1486_*1489del, XM_005272552.4:c.*1486GA[1], XM_005272552.4:c.*1486GA[4], XM_005272552.3:c.*1486_*1489del, XM_005272552.3:c.*1486GA[1], XM_005272552.3:c.*1486GA[4], XM_005272552.2:c.*1486_*1489del, XM_005272552.2:c.*1486GA[1], XM_005272552.2:c.*1486GA[4], XM_005272552.1:c.*1486_*1489del, XM_005272552.1:c.*1486GA[1], XM_005272552.1:c.*1486GA[4], XM_011543880.4:c.*1486_*1489del, XM_011543880.4:c.*1486GA[1], XM_011543880.4:c.*1486GA[4], XM_011543880.3:c.*1486_*1489del, XM_011543880.3:c.*1486GA[1], XM_011543880.3:c.*1486GA[4], XM_011543880.2:c.*1486_*1489del, XM_011543880.2:c.*1486GA[1], XM_011543880.2:c.*1486GA[4], XM_011543880.1:c.*1486_*1489del, XM_011543880.1:c.*1486GA[1], XM_011543880.1:c.*1486GA[4], XM_005272550.4:c.*1486_*1489del, XM_005272550.4:c.*1486GA[1], XM_005272550.4:c.*1486GA[4], XM_005272550.3:c.*1486_*1489del, XM_005272550.3:c.*1486GA[1], XM_005272550.3:c.*1486GA[4], XM_005272550.2:c.*1486_*1489del, XM_005272550.2:c.*1486GA[1], XM_005272550.2:c.*1486GA[4], XM_005272550.1:c.*1486_*1489del, XM_005272550.1:c.*1486GA[1], XM_005272550.1:c.*1486GA[4], XM_011543879.4:c.*1486_*1489del, XM_011543879.4:c.*1486GA[1], XM_011543879.4:c.*1486GA[4], XM_011543879.3:c.*1486_*1489del, XM_011543879.3:c.*1486GA[1], XM_011543879.3:c.*1486GA[4], XM_011543879.2:c.*1486_*1489del, XM_011543879.2:c.*1486GA[1], XM_011543879.2:c.*1486GA[4], XM_011543879.1:c.*1486_*1489del, XM_011543879.1:c.*1486GA[1], XM_011543879.1:c.*1486GA[4], XM_017022651.3:c.*1486_*1489del, XM_017022651.3:c.*1486GA[1], XM_017022651.3:c.*1486GA[4], XM_017022651.2:c.*1486_*1489del, XM_017022651.2:c.*1486GA[1], XM_017022651.2:c.*1486GA[4], XM_017022651.1:c.*1486_*1489del, XM_017022651.1:c.*1486GA[1], XM_017022651.1:c.*1486GA[4], XM_017022653.3:c.*1486_*1489del, XM_017022653.3:c.*1486GA[1], XM_017022653.3:c.*1486GA[4], XM_017022653.2:c.*1486_*1489del, XM_017022653.2:c.*1486GA[1], XM_017022653.2:c.*1486GA[4], XM_017022653.1:c.*1486_*1489del, XM_017022653.1:c.*1486GA[1], XM_017022653.1:c.*1486GA[4], XM_011543877.3:c.*1486_*1489del, XM_011543877.3:c.*1486GA[1], XM_011543877.3:c.*1486GA[4], XM_011543877.2:c.*1486_*1489del, XM_011543877.2:c.*1486GA[1], XM_011543877.2:c.*1486GA[4], XM_011543877.1:c.*1486_*1489del, XM_011543877.1:c.*1486GA[1], XM_011543877.1:c.*1486GA[4], XM_017022649.3:c.*1486_*1489del, XM_017022649.3:c.*1486GA[1], XM_017022649.3:c.*1486GA[4], XM_017022649.2:c.*1486_*1489del, XM_017022649.2:c.*1486GA[1], XM_017022649.2:c.*1486GA[4], XM_017022649.1:c.*1486_*1489del, XM_017022649.1:c.*1486GA[1], XM_017022649.1:c.*1486GA[4], XM_017022650.3:c.*1486_*1489del, XM_017022650.3:c.*1486GA[1], XM_017022650.3:c.*1486GA[4], XM_017022650.2:c.*1486_*1489del, XM_017022650.2:c.*1486GA[1], XM_017022650.2:c.*1486GA[4], XM_017022650.1:c.*1486_*1489del, XM_017022650.1:c.*1486GA[1], XM_017022650.1:c.*1486GA[4], XM_006720364.3:c.*1486_*1489del, XM_006720364.3:c.*1486GA[1], XM_006720364.3:c.*1486GA[4], XM_006720364.2:c.*1486_*1489del, XM_006720364.2:c.*1486GA[1], XM_006720364.2:c.*1486GA[4], XM_006720364.1:c.*1486_*1489del, XM_006720364.1:c.*1486GA[1], XM_006720364.1:c.*1486GA[4], XM_017022652.3:c.*1486_*1489del, XM_017022652.3:c.*1486GA[1], XM_017022652.3:c.*1486GA[4], XM_017022652.2:c.*1486_*1489del, XM_017022652.2:c.*1486GA[1], XM_017022652.2:c.*1486GA[4], XM_017022652.1:c.*1486_*1489del, XM_017022652.1:c.*1486GA[1], XM_017022652.1:c.*1486GA[4], XM_017022654.3:c.*1486_*1489del, XM_017022654.3:c.*1486GA[1], XM_017022654.3:c.*1486GA[4], XM_017022654.2:c.*1486_*1489del, XM_017022654.2:c.*1486GA[1], XM_017022654.2:c.*1486GA[4], XM_017022654.1:c.*1486_*1489del, XM_017022654.1:c.*1486GA[1], XM_017022654.1:c.*1486GA[4], XM_017022645.2:c.*1486_*1489del, XM_017022645.2:c.*1486GA[1], XM_017022645.2:c.*1486GA[4], XM_017022645.1:c.*1486_*1489del, XM_017022645.1:c.*1486GA[1], XM_017022645.1:c.*1486GA[4], XM_017022648.2:c.*1486_*1489del, XM_017022648.2:c.*1486GA[1], XM_017022648.2:c.*1486GA[4], XM_017022648.1:c.*1486_*1489del, XM_017022648.1:c.*1486GA[1], XM_017022648.1:c.*1486GA[4], XM_006720367.2:c.*1486_*1489del, XM_006720367.2:c.*1486GA[1], XM_006720367.2:c.*1486GA[4], XM_006720367.1:c.*1486_*1489del, XM_006720367.1:c.*1486GA[1], XM_006720367.1:c.*1486GA[4], XM_017022646.2:c.*1486_*1489del, XM_017022646.2:c.*1486GA[1], XM_017022646.2:c.*1486GA[4], XM_017022646.1:c.*1486_*1489del, XM_017022646.1:c.*1486GA[1], XM_017022646.1:c.*1486GA[4], XM_017022647.2:c.*1486_*1489del, XM_017022647.2:c.*1486GA[1], XM_017022647.2:c.*1486GA[4], XM_017022647.1:c.*1486_*1489del, XM_017022647.1:c.*1486GA[1], XM_017022647.1:c.*1486GA[4], XM_017022660.2:c.*1486_*1489del, XM_017022660.2:c.*1486GA[1], XM_017022660.2:c.*1486GA[4], XM_017022660.1:c.*1486_*1489del, XM_017022660.1:c.*1486GA[1], XM_017022660.1:c.*1486GA[4], XM_017022657.2:c.*1486_*1489del, XM_017022657.2:c.*1486GA[1], XM_017022657.2:c.*1486GA[4], XM_017022657.1:c.*1486_*1489del, XM_017022657.1:c.*1486GA[1], XM_017022657.1:c.*1486GA[4], XM_017022659.2:c.*1486_*1489del, XM_017022659.2:c.*1486GA[1], XM_017022659.2:c.*1486GA[4], XM_017022659.1:c.*1486_*1489del, XM_017022659.1:c.*1486GA[1], XM_017022659.1:c.*1486GA[4], XM_017022655.2:c.*1486_*1489del, XM_017022655.2:c.*1486GA[1], XM_017022655.2:c.*1486GA[4], XM_017022655.1:c.*1486_*1489del, XM_017022655.1:c.*1486GA[1], XM_017022655.1:c.*1486GA[4], XM_017022662.2:c.*1486_*1489del, XM_017022662.2:c.*1486GA[1], XM_017022662.2:c.*1486GA[4], XM_017022662.1:c.*1486_*1489del, XM_017022662.1:c.*1486GA[1], XM_017022662.1:c.*1486GA[4], XM_017022661.2:c.*1486_*1489del, XM_017022661.2:c.*1486GA[1], XM_017022661.2:c.*1486GA[4], XM_017022661.1:c.*1486_*1489del, XM_017022661.1:c.*1486GA[1], XM_017022661.1:c.*1486GA[4], XM_017022658.2:c.*1486_*1489del, XM_017022658.2:c.*1486GA[1], XM_017022658.2:c.*1486GA[4], XM_017022658.1:c.*1486_*1489del, XM_017022658.1:c.*1486GA[1], XM_017022658.1:c.*1486GA[4], XM_017022663.2:c.*1486_*1489del, XM_017022663.2:c.*1486GA[1], XM_017022663.2:c.*1486GA[4], XM_017022663.1:c.*1486_*1489del, XM_017022663.1:c.*1486GA[1], XM_017022663.1:c.*1486GA[4], XM_047433159.1:c.*1486_*1489del, XM_047433159.1:c.*1486GA[1], XM_047433159.1:c.*1486GA[4], XM_017022656.2:c.*1486_*1489del, XM_017022656.2:c.*1486GA[1], XM_017022656.2:c.*1486GA[4], XM_017022656.1:c.*1486_*1489del, XM_017022656.1:c.*1486GA[1], XM_017022656.1:c.*1486GA[4], XM_047433158.1:c.*1486_*1489del, XM_047433158.1:c.*1486GA[1], XM_047433158.1:c.*1486GA[4], XM_047433153.1:c.*1486_*1489del, XM_047433153.1:c.*1486GA[1], XM_047433153.1:c.*1486GA[4], XM_047433163.1:c.*1486_*1489del, XM_047433163.1:c.*1486GA[1], XM_047433163.1:c.*1486GA[4], XM_047433154.1:c.*1486_*1489del, XM_047433154.1:c.*1486GA[1], XM_047433154.1:c.*1486GA[4], XM_047433152.1:c.*1486_*1489del, XM_047433152.1:c.*1486GA[1], XM_047433152.1:c.*1486GA[4], XM_047433156.1:c.*1486_*1489del, XM_047433156.1:c.*1486GA[1], XM_047433156.1:c.*1486GA[4], XM_047433150.1:c.*1486_*1489del, XM_047433150.1:c.*1486GA[1], XM_047433150.1:c.*1486GA[4], XM_047433151.1:c.*1486_*1489del, XM_047433151.1:c.*1486GA[1], XM_047433151.1:c.*1486GA[4], XM_047433162.1:c.*1486_*1489del, XM_047433162.1:c.*1486GA[1], XM_047433162.1:c.*1486GA[4], XM_047433160.1:c.*1486_*1489del, XM_047433160.1:c.*1486GA[1], XM_047433160.1:c.*1486GA[4], XM_047433157.1:c.*1486_*1489del, XM_047433157.1:c.*1486GA[1], XM_047433157.1:c.*1486GA[4], XM_047433161.1:c.*1486_*1489del, XM_047433161.1:c.*1486GA[1], XM_047433161.1:c.*1486GA[4], XM_047433155.1:c.*1486_*1489del, XM_047433155.1:c.*1486GA[1], XM_047433155.1:c.*1486GA[4]

                  9.

                  rs1491157226 has merged into rs146187627 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    ->GTTA [Show Flanks]
                    Chromosome:
                    15:22867541 (GRCh38)
                    15:23005522 (GRCh37)
                    Canonical SPDI:
                    NC_000015.10:22867541:AGTTA:AGTTAGTTA
                    Gene:
                    CYFIP1 (Varview), NIPA2 (Varview)
                    Functional Consequence:
                    3_prime_UTR_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    AGTTAGTTA=0.00843/100 (ALFA)
                    AGTT=0.01178/3118 (TOPMED)
                    AGTT=0.01192/1671 (GnomAD)
                    AGTT=0.012336/62 (1000Genomes)
                    HGVS:
                    NC_000015.10:g.22867543_22867546dup, NC_000015.9:g.23005523_23005526dup, NG_054889.1:g.118362_118365dup, NM_014608.6:c.*2483_*2486dup, NM_014608.5:c.*2483_*2486dup, NM_001287810.4:c.*2483_*2486dup, NM_001287810.3:c.*2483_*2486dup, NM_001324122.3:c.*2483_*2486dup, NM_001324122.2:c.*2483_*2486dup, NM_001324123.3:c.*2483_*2486dup, NM_001324123.2:c.*2483_*2486dup, NM_001324124.3:c.*2483_*2486dup, NM_001324124.2:c.*2483_*2486dup, NM_001324126.3:c.*2483_*2486dup, NM_001324126.2:c.*2483_*2486dup, NM_001324125.3:c.*2483_*2486dup, NM_001324125.2:c.*2483_*2486dup, NM_001033028.3:c.*2483_*2486dup, NM_001033028.2:c.*2483_*2486dup, NM_001324120.2:c.*2483_*2486dup, NM_001324119.2:c.*2483_*2486dup, NG_021303.1:g.33903_33906dup, NM_030922.7:c.*696_*699dup, NM_030922.6:c.*696_*699dup, NM_001008860.3:c.*696_*699dup, NM_001008860.2:c.*696_*699dup, NM_001008892.3:c.*696_*699dup, NM_001008892.2:c.*696_*699dup, NM_001008894.3:c.*696_*699dup, NM_001008894.2:c.*696_*699dup, NM_001184889.2:c.*696_*699dup, NM_001184889.1:c.*696_*699dup, NM_001184888.2:c.*696_*699dup, NM_001184888.1:c.*696_*699dup, NW_021160017.1:g.3761618_3761621dup, XM_005272548.4:c.*696_*699dup, XM_005272548.3:c.*696_*699dup, XM_005272548.2:c.*696_*699dup, XM_005272548.1:c.*696_*699dup, XM_005272553.6:c.*696_*699dup, XM_005272553.5:c.*696_*699dup, XM_005272553.4:c.*696_*699dup, XM_005272553.3:c.*696_*699dup, XM_005272553.2:c.*696_*699dup, XM_005272553.1:c.*696_*699dup, XM_011543878.4:c.*696_*699dup, XM_011543878.3:c.*696_*699dup, XM_011543878.2:c.*696_*699dup, XM_011543878.1:c.*696_*699dup, XM_005272546.4:c.*696_*699dup, XM_005272546.3:c.*696_*699dup, XM_005272546.2:c.*696_*699dup, XM_005272546.1:c.*696_*699dup, XM_005272547.5:c.*696_*699dup, XM_005272547.4:c.*696_*699dup, XM_005272547.3:c.*696_*699dup, XM_005272547.2:c.*696_*699dup, XM_005272547.1:c.*696_*699dup, XM_005272552.5:c.*696_*699dup, XM_005272552.4:c.*696_*699dup, XM_005272552.3:c.*696_*699dup, XM_005272552.2:c.*696_*699dup, XM_005272552.1:c.*696_*699dup, XM_011543880.4:c.*696_*699dup, XM_011543880.3:c.*696_*699dup, XM_011543880.2:c.*696_*699dup, XM_011543880.1:c.*696_*699dup, XM_005272550.4:c.*696_*699dup, XM_005272550.3:c.*696_*699dup, XM_005272550.2:c.*696_*699dup, XM_005272550.1:c.*696_*699dup, XM_011543879.4:c.*696_*699dup, XM_011543879.3:c.*696_*699dup, XM_011543879.2:c.*696_*699dup, XM_011543879.1:c.*696_*699dup, XM_017022651.3:c.*696_*699dup, XM_017022651.2:c.*696_*699dup, XM_017022651.1:c.*696_*699dup, XM_017022653.3:c.*696_*699dup, XM_017022653.2:c.*696_*699dup, XM_017022653.1:c.*696_*699dup, XM_011543877.3:c.*696_*699dup, XM_011543877.2:c.*696_*699dup, XM_011543877.1:c.*696_*699dup, XM_017022649.3:c.*696_*699dup, XM_017022649.2:c.*696_*699dup, XM_017022649.1:c.*696_*699dup, XM_017022650.3:c.*696_*699dup, XM_017022650.2:c.*696_*699dup, XM_017022650.1:c.*696_*699dup, XM_006720364.3:c.*696_*699dup, XM_006720364.2:c.*696_*699dup, XM_006720364.1:c.*696_*699dup, XM_017022652.3:c.*696_*699dup, XM_017022652.2:c.*696_*699dup, XM_017022652.1:c.*696_*699dup, XM_017022654.3:c.*696_*699dup, XM_017022654.2:c.*696_*699dup, XM_017022654.1:c.*696_*699dup, XM_017022645.2:c.*696_*699dup, XM_017022645.1:c.*696_*699dup, XM_017022646.2:c.*696_*699dup, XM_017022646.1:c.*696_*699dup, XM_017022647.2:c.*696_*699dup, XM_017022647.1:c.*696_*699dup, XM_017022660.2:c.*696_*699dup, XM_017022660.1:c.*696_*699dup, XM_017022657.2:c.*696_*699dup, XM_017022657.1:c.*696_*699dup, XM_017022659.2:c.*696_*699dup, XM_017022659.1:c.*696_*699dup, XM_017022656.2:c.*696_*699dup, XM_017022656.1:c.*696_*699dup, XM_017022655.2:c.*696_*699dup, XM_017022655.1:c.*696_*699dup, XM_017022662.2:c.*696_*699dup, XM_017022662.1:c.*696_*699dup, XM_017022661.2:c.*696_*699dup, XM_017022661.1:c.*696_*699dup, XM_017022658.2:c.*696_*699dup, XM_017022658.1:c.*696_*699dup, XM_017022663.2:c.*696_*699dup, XM_017022663.1:c.*696_*699dup, XM_017022648.2:c.*696_*699dup, XM_017022648.1:c.*696_*699dup, XM_006720367.2:c.*696_*699dup, XM_006720367.1:c.*696_*699dup, XM_047433156.1:c.*696_*699dup, XM_047433150.1:c.*696_*699dup, XM_047433155.1:c.*696_*699dup, XM_047433158.1:c.*696_*699dup, XM_047433151.1:c.*696_*699dup, XM_047433162.1:c.*696_*699dup, XM_047433154.1:c.*696_*699dup, XM_047433157.1:c.*696_*699dup, XM_047433153.1:c.*696_*699dup, XM_047433163.1:c.*696_*699dup, XM_047433152.1:c.*696_*699dup, XM_047433161.1:c.*696_*699dup, XM_047433159.1:c.*696_*699dup, XM_047433160.1:c.*696_*699dup

                    10.

                    rs1491135183 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      ->GTT,TGTT [Show Flanks]
                      Chromosome:
                      15:22867696 (GRCh38)
                      15:23005368 (GRCh37)
                      Canonical SPDI:
                      NC_000015.10:22867696:TGTT:TGTTGTT,NC_000015.10:22867696:TGTT:TGTTTGTT
                      Gene:
                      CYFIP1 (Varview), NIPA2 (Varview)
                      Functional Consequence:
                      3_prime_UTR_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      TGTTTGTT=0./0 (ALFA)
                      TGT=0.000007/1 (GnomAD)
                      HGVS:
                      NC_000015.10:g.22867698_22867700dup, NC_000015.10:g.22867697_22867700dup, NC_000015.9:g.23005369_23005371dup, NC_000015.9:g.23005368_23005371dup, NG_054889.1:g.118208_118210dup, NG_054889.1:g.118207_118210dup, NM_014608.6:c.*2329_*2331dup, NM_014608.6:c.*2328_*2331dup, NM_014608.5:c.*2329_*2331dup, NM_014608.5:c.*2328_*2331dup, NM_001287810.4:c.*2329_*2331dup, NM_001287810.4:c.*2328_*2331dup, NM_001287810.3:c.*2329_*2331dup, NM_001287810.3:c.*2328_*2331dup, NM_001324122.3:c.*2329_*2331dup, NM_001324122.3:c.*2328_*2331dup, NM_001324122.2:c.*2329_*2331dup, NM_001324122.2:c.*2328_*2331dup, NM_001324123.3:c.*2329_*2331dup, NM_001324123.3:c.*2328_*2331dup, NM_001324123.2:c.*2329_*2331dup, NM_001324123.2:c.*2328_*2331dup, NM_001324124.3:c.*2329_*2331dup, NM_001324124.3:c.*2328_*2331dup, NM_001324124.2:c.*2329_*2331dup, NM_001324124.2:c.*2328_*2331dup, NM_001324126.3:c.*2329_*2331dup, NM_001324126.3:c.*2328_*2331dup, NM_001324126.2:c.*2329_*2331dup, NM_001324126.2:c.*2328_*2331dup, NM_001324125.3:c.*2329_*2331dup, NM_001324125.3:c.*2328_*2331dup, NM_001324125.2:c.*2329_*2331dup, NM_001324125.2:c.*2328_*2331dup, NM_001033028.3:c.*2329_*2331dup, NM_001033028.3:c.*2328_*2331dup, NM_001033028.2:c.*2329_*2331dup, NM_001033028.2:c.*2328_*2331dup, NM_001324120.2:c.*2329_*2331dup, NM_001324120.2:c.*2328_*2331dup, NM_001324119.2:c.*2329_*2331dup, NM_001324119.2:c.*2328_*2331dup, NG_021303.1:g.34058_34060dup, NG_021303.1:g.34057_34060dup, NM_030922.7:c.*851_*853dup, NM_030922.7:c.*850_*853dup, NM_030922.6:c.*851_*853dup, NM_030922.6:c.*850_*853dup, NM_001008860.3:c.*851_*853dup, NM_001008860.3:c.*850_*853dup, NM_001008860.2:c.*851_*853dup, NM_001008860.2:c.*850_*853dup, NM_001008892.3:c.*851_*853dup, NM_001008892.3:c.*850_*853dup, NM_001008892.2:c.*851_*853dup, NM_001008892.2:c.*850_*853dup, NM_001008894.3:c.*851_*853dup, NM_001008894.3:c.*850_*853dup, NM_001008894.2:c.*851_*853dup, NM_001008894.2:c.*850_*853dup, NM_001184889.2:c.*851_*853dup, NM_001184889.2:c.*850_*853dup, NM_001184889.1:c.*851_*853dup, NM_001184889.1:c.*850_*853dup, NM_001184888.2:c.*851_*853dup, NM_001184888.2:c.*850_*853dup, NM_001184888.1:c.*851_*853dup, NM_001184888.1:c.*850_*853dup, NW_021160017.1:g.3761774_3761776dup, NW_021160017.1:g.3761773_3761776dup, XM_005272548.4:c.*851_*853dup, XM_005272548.4:c.*850_*853dup, XM_005272548.3:c.*851_*853dup, XM_005272548.3:c.*850_*853dup, XM_005272548.2:c.*851_*853dup, XM_005272548.2:c.*850_*853dup, XM_005272548.1:c.*851_*853dup, XM_005272548.1:c.*850_*853dup, XM_005272553.6:c.*851_*853dup, XM_005272553.6:c.*850_*853dup, XM_005272553.5:c.*851_*853dup, XM_005272553.5:c.*850_*853dup, XM_005272553.4:c.*851_*853dup, XM_005272553.4:c.*850_*853dup, XM_005272553.3:c.*851_*853dup, XM_005272553.3:c.*850_*853dup, XM_005272553.2:c.*851_*853dup, XM_005272553.2:c.*850_*853dup, XM_005272553.1:c.*851_*853dup, XM_005272553.1:c.*850_*853dup, XM_011543878.4:c.*851_*853dup, XM_011543878.4:c.*850_*853dup, XM_011543878.3:c.*851_*853dup, XM_011543878.3:c.*850_*853dup, XM_011543878.2:c.*851_*853dup, XM_011543878.2:c.*850_*853dup, XM_011543878.1:c.*851_*853dup, XM_011543878.1:c.*850_*853dup, XM_005272546.4:c.*851_*853dup, XM_005272546.4:c.*850_*853dup, XM_005272546.3:c.*851_*853dup, XM_005272546.3:c.*850_*853dup, XM_005272546.2:c.*851_*853dup, XM_005272546.2:c.*850_*853dup, XM_005272546.1:c.*851_*853dup, XM_005272546.1:c.*850_*853dup, XM_005272547.5:c.*851_*853dup, XM_005272547.5:c.*850_*853dup, XM_005272547.4:c.*851_*853dup, XM_005272547.4:c.*850_*853dup, XM_005272547.3:c.*851_*853dup, XM_005272547.3:c.*850_*853dup, XM_005272547.2:c.*851_*853dup, XM_005272547.2:c.*850_*853dup, XM_005272547.1:c.*851_*853dup, XM_005272547.1:c.*850_*853dup, XM_005272552.5:c.*851_*853dup, XM_005272552.5:c.*850_*853dup, XM_005272552.4:c.*851_*853dup, XM_005272552.4:c.*850_*853dup, XM_005272552.3:c.*851_*853dup, XM_005272552.3:c.*850_*853dup, XM_005272552.2:c.*851_*853dup, XM_005272552.2:c.*850_*853dup, XM_005272552.1:c.*851_*853dup, XM_005272552.1:c.*850_*853dup, XM_011543880.4:c.*851_*853dup, XM_011543880.4:c.*850_*853dup, XM_011543880.3:c.*851_*853dup, XM_011543880.3:c.*850_*853dup, XM_011543880.2:c.*851_*853dup, XM_011543880.2:c.*850_*853dup, XM_011543880.1:c.*851_*853dup, XM_011543880.1:c.*850_*853dup, XM_005272550.4:c.*851_*853dup, XM_005272550.4:c.*850_*853dup, XM_005272550.3:c.*851_*853dup, XM_005272550.3:c.*850_*853dup, XM_005272550.2:c.*851_*853dup, XM_005272550.2:c.*850_*853dup, XM_005272550.1:c.*851_*853dup, XM_005272550.1:c.*850_*853dup, XM_011543879.4:c.*851_*853dup, XM_011543879.4:c.*850_*853dup, XM_011543879.3:c.*851_*853dup, XM_011543879.3:c.*850_*853dup, XM_011543879.2:c.*851_*853dup, XM_011543879.2:c.*850_*853dup, XM_011543879.1:c.*851_*853dup, XM_011543879.1:c.*850_*853dup, XM_017022651.3:c.*851_*853dup, XM_017022651.3:c.*850_*853dup, XM_017022651.2:c.*851_*853dup, XM_017022651.2:c.*850_*853dup, XM_017022651.1:c.*851_*853dup, XM_017022651.1:c.*850_*853dup, XM_017022653.3:c.*851_*853dup, XM_017022653.3:c.*850_*853dup, XM_017022653.2:c.*851_*853dup, XM_017022653.2:c.*850_*853dup, XM_017022653.1:c.*851_*853dup, XM_017022653.1:c.*850_*853dup, XM_011543877.3:c.*851_*853dup, XM_011543877.3:c.*850_*853dup, XM_011543877.2:c.*851_*853dup, XM_011543877.2:c.*850_*853dup, XM_011543877.1:c.*851_*853dup, XM_011543877.1:c.*850_*853dup, XM_017022649.3:c.*851_*853dup, XM_017022649.3:c.*850_*853dup, XM_017022649.2:c.*851_*853dup, XM_017022649.2:c.*850_*853dup, XM_017022649.1:c.*851_*853dup, XM_017022649.1:c.*850_*853dup, XM_017022650.3:c.*851_*853dup, XM_017022650.3:c.*850_*853dup, XM_017022650.2:c.*851_*853dup, XM_017022650.2:c.*850_*853dup, XM_017022650.1:c.*851_*853dup, XM_017022650.1:c.*850_*853dup, XM_006720364.3:c.*851_*853dup, XM_006720364.3:c.*850_*853dup, XM_006720364.2:c.*851_*853dup, XM_006720364.2:c.*850_*853dup, XM_006720364.1:c.*851_*853dup, XM_006720364.1:c.*850_*853dup, XM_017022652.3:c.*851_*853dup, XM_017022652.3:c.*850_*853dup, XM_017022652.2:c.*851_*853dup, XM_017022652.2:c.*850_*853dup, XM_017022652.1:c.*851_*853dup, XM_017022652.1:c.*850_*853dup, XM_017022654.3:c.*851_*853dup, XM_017022654.3:c.*850_*853dup, XM_017022654.2:c.*851_*853dup, XM_017022654.2:c.*850_*853dup, XM_017022654.1:c.*851_*853dup, XM_017022654.1:c.*850_*853dup, XM_017022645.2:c.*851_*853dup, XM_017022645.2:c.*850_*853dup, XM_017022645.1:c.*851_*853dup, XM_017022645.1:c.*850_*853dup, XM_017022646.2:c.*851_*853dup, XM_017022646.2:c.*850_*853dup, XM_017022646.1:c.*851_*853dup, XM_017022646.1:c.*850_*853dup, XM_017022647.2:c.*851_*853dup, XM_017022647.2:c.*850_*853dup, XM_017022647.1:c.*851_*853dup, XM_017022647.1:c.*850_*853dup, XM_017022660.2:c.*851_*853dup, XM_017022660.2:c.*850_*853dup, XM_017022660.1:c.*851_*853dup, XM_017022660.1:c.*850_*853dup, XM_017022657.2:c.*851_*853dup, XM_017022657.2:c.*850_*853dup, XM_017022657.1:c.*851_*853dup, XM_017022657.1:c.*850_*853dup, XM_017022659.2:c.*851_*853dup, XM_017022659.2:c.*850_*853dup, XM_017022659.1:c.*851_*853dup, XM_017022659.1:c.*850_*853dup, XM_017022656.2:c.*851_*853dup, XM_017022656.2:c.*850_*853dup, XM_017022656.1:c.*851_*853dup, XM_017022656.1:c.*850_*853dup, XM_017022655.2:c.*851_*853dup, XM_017022655.2:c.*850_*853dup, XM_017022655.1:c.*851_*853dup, XM_017022655.1:c.*850_*853dup, XM_017022662.2:c.*851_*853dup, XM_017022662.2:c.*850_*853dup, XM_017022662.1:c.*851_*853dup, XM_017022662.1:c.*850_*853dup, XM_017022661.2:c.*851_*853dup, XM_017022661.2:c.*850_*853dup, XM_017022661.1:c.*851_*853dup, XM_017022661.1:c.*850_*853dup, XM_017022658.2:c.*851_*853dup, XM_017022658.2:c.*850_*853dup, XM_017022658.1:c.*851_*853dup, XM_017022658.1:c.*850_*853dup, XM_017022663.2:c.*851_*853dup, XM_017022663.2:c.*850_*853dup, XM_017022663.1:c.*851_*853dup, XM_017022663.1:c.*850_*853dup, XM_017022648.2:c.*851_*853dup, XM_017022648.2:c.*850_*853dup, XM_017022648.1:c.*851_*853dup, XM_017022648.1:c.*850_*853dup, XM_006720367.2:c.*851_*853dup, XM_006720367.2:c.*850_*853dup, XM_006720367.1:c.*851_*853dup, XM_006720367.1:c.*850_*853dup, XM_047433156.1:c.*851_*853dup, XM_047433156.1:c.*850_*853dup, XM_047433150.1:c.*851_*853dup, XM_047433150.1:c.*850_*853dup, XM_047433155.1:c.*851_*853dup, XM_047433155.1:c.*850_*853dup, XM_047433158.1:c.*851_*853dup, XM_047433158.1:c.*850_*853dup, XM_047433151.1:c.*851_*853dup, XM_047433151.1:c.*850_*853dup, XM_047433162.1:c.*851_*853dup, XM_047433162.1:c.*850_*853dup, XM_047433154.1:c.*851_*853dup, XM_047433154.1:c.*850_*853dup, XM_047433157.1:c.*851_*853dup, XM_047433157.1:c.*850_*853dup, XM_047433153.1:c.*851_*853dup, XM_047433153.1:c.*850_*853dup, XM_047433163.1:c.*851_*853dup, XM_047433163.1:c.*850_*853dup, XM_047433152.1:c.*851_*853dup, XM_047433152.1:c.*850_*853dup, XM_047433161.1:c.*851_*853dup, XM_047433161.1:c.*850_*853dup, XM_047433159.1:c.*851_*853dup, XM_047433159.1:c.*850_*853dup, XM_047433160.1:c.*851_*853dup, XM_047433160.1:c.*850_*853dup

                      11.

                      rs1491113493 [Homo sapiens]
                        Variant type:
                        DEL
                        Alleles:
                        AT>- [Show Flanks]
                        Chromosome:
                        15:22867696 (GRCh38)
                        15:23005371 (GRCh37)
                        Canonical SPDI:
                        NC_000015.10:22867695:AT:
                        Gene:
                        CYFIP1 (Varview), NIPA2 (Varview)
                        Functional Consequence:
                        3_prime_UTR_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        -=0./0 (ALFA)
                        -=0.000128/34 (TOPMED)
                        -=0.000143/20 (GnomAD)
                        HGVS:
                        NC_000015.10:g.22867696_22867697del, NC_000015.9:g.23005371_23005372del, NG_054889.1:g.118210_118211del, NM_014608.6:c.*2331_*2332del, NM_014608.5:c.*2331_*2332del, NM_001287810.4:c.*2331_*2332del, NM_001287810.3:c.*2331_*2332del, NM_001324122.3:c.*2331_*2332del, NM_001324122.2:c.*2331_*2332del, NM_001324123.3:c.*2331_*2332del, NM_001324123.2:c.*2331_*2332del, NM_001324124.3:c.*2331_*2332del, NM_001324124.2:c.*2331_*2332del, NM_001324126.3:c.*2331_*2332del, NM_001324126.2:c.*2331_*2332del, NM_001324125.3:c.*2331_*2332del, NM_001324125.2:c.*2331_*2332del, NM_001033028.3:c.*2331_*2332del, NM_001033028.2:c.*2331_*2332del, NM_001324120.2:c.*2331_*2332del, NM_001324119.2:c.*2331_*2332del, NG_021303.1:g.34056_34057del, NM_030922.7:c.*849_*850del, NM_030922.6:c.*849_*850del, NM_001008860.3:c.*849_*850del, NM_001008860.2:c.*849_*850del, NM_001008892.3:c.*849_*850del, NM_001008892.2:c.*849_*850del, NM_001008894.3:c.*849_*850del, NM_001008894.2:c.*849_*850del, NM_001184889.2:c.*849_*850del, NM_001184889.1:c.*849_*850del, NM_001184888.2:c.*849_*850del, NM_001184888.1:c.*849_*850del, NW_021160017.1:g.3761772_3761773del, XM_005272548.4:c.*849_*850del, XM_005272548.3:c.*849_*850del, XM_005272548.2:c.*849_*850del, XM_005272548.1:c.*849_*850del, XM_005272553.6:c.*849_*850del, XM_005272553.5:c.*849_*850del, XM_005272553.4:c.*849_*850del, XM_005272553.3:c.*849_*850del, XM_005272553.2:c.*849_*850del, XM_005272553.1:c.*849_*850del, XM_011543878.4:c.*849_*850del, XM_011543878.3:c.*849_*850del, XM_011543878.2:c.*849_*850del, XM_011543878.1:c.*849_*850del, XM_005272546.4:c.*849_*850del, XM_005272546.3:c.*849_*850del, XM_005272546.2:c.*849_*850del, XM_005272546.1:c.*849_*850del, XM_005272547.5:c.*849_*850del, XM_005272547.4:c.*849_*850del, XM_005272547.3:c.*849_*850del, XM_005272547.2:c.*849_*850del, XM_005272547.1:c.*849_*850del, XM_005272552.5:c.*849_*850del, XM_005272552.4:c.*849_*850del, XM_005272552.3:c.*849_*850del, XM_005272552.2:c.*849_*850del, XM_005272552.1:c.*849_*850del, XM_011543880.4:c.*849_*850del, XM_011543880.3:c.*849_*850del, XM_011543880.2:c.*849_*850del, XM_011543880.1:c.*849_*850del, XM_005272550.4:c.*849_*850del, XM_005272550.3:c.*849_*850del, XM_005272550.2:c.*849_*850del, XM_005272550.1:c.*849_*850del, XM_011543879.4:c.*849_*850del, XM_011543879.3:c.*849_*850del, XM_011543879.2:c.*849_*850del, XM_011543879.1:c.*849_*850del, XM_017022651.3:c.*849_*850del, XM_017022651.2:c.*849_*850del, XM_017022651.1:c.*849_*850del, XM_017022653.3:c.*849_*850del, XM_017022653.2:c.*849_*850del, XM_017022653.1:c.*849_*850del, XM_011543877.3:c.*849_*850del, XM_011543877.2:c.*849_*850del, XM_011543877.1:c.*849_*850del, XM_017022649.3:c.*849_*850del, XM_017022649.2:c.*849_*850del, XM_017022649.1:c.*849_*850del, XM_017022650.3:c.*849_*850del, XM_017022650.2:c.*849_*850del, XM_017022650.1:c.*849_*850del, XM_006720364.3:c.*849_*850del, XM_006720364.2:c.*849_*850del, XM_006720364.1:c.*849_*850del, XM_017022652.3:c.*849_*850del, XM_017022652.2:c.*849_*850del, XM_017022652.1:c.*849_*850del, XM_017022654.3:c.*849_*850del, XM_017022654.2:c.*849_*850del, XM_017022654.1:c.*849_*850del, XM_017022645.2:c.*849_*850del, XM_017022645.1:c.*849_*850del, XM_017022646.2:c.*849_*850del, XM_017022646.1:c.*849_*850del, XM_017022647.2:c.*849_*850del, XM_017022647.1:c.*849_*850del, XM_017022660.2:c.*849_*850del, XM_017022660.1:c.*849_*850del, XM_017022657.2:c.*849_*850del, XM_017022657.1:c.*849_*850del, XM_017022659.2:c.*849_*850del, XM_017022659.1:c.*849_*850del, XM_017022656.2:c.*849_*850del, XM_017022656.1:c.*849_*850del, XM_017022655.2:c.*849_*850del, XM_017022655.1:c.*849_*850del, XM_017022662.2:c.*849_*850del, XM_017022662.1:c.*849_*850del, XM_017022661.2:c.*849_*850del, XM_017022661.1:c.*849_*850del, XM_017022658.2:c.*849_*850del, XM_017022658.1:c.*849_*850del, XM_017022663.2:c.*849_*850del, XM_017022663.1:c.*849_*850del, XM_017022648.2:c.*849_*850del, XM_017022648.1:c.*849_*850del, XM_006720367.2:c.*849_*850del, XM_006720367.1:c.*849_*850del, XM_047433156.1:c.*849_*850del, XM_047433150.1:c.*849_*850del, XM_047433155.1:c.*849_*850del, XM_047433158.1:c.*849_*850del, XM_047433151.1:c.*849_*850del, XM_047433162.1:c.*849_*850del, XM_047433154.1:c.*849_*850del, XM_047433157.1:c.*849_*850del, XM_047433153.1:c.*849_*850del, XM_047433163.1:c.*849_*850del, XM_047433152.1:c.*849_*850del, XM_047433161.1:c.*849_*850del, XM_047433159.1:c.*849_*850del, XM_047433160.1:c.*849_*850del

                        12.

                        rs1491078441 has merged into rs565918417 [Homo sapiens]
                          Variant type:
                          DELINS
                          Alleles:
                          GA>- [Show Flanks]
                          Chromosome:
                          15:22868306 (GRCh38)
                          15:23004762 (GRCh37)
                          Canonical SPDI:
                          NC_000015.10:22868304:AGA:A
                          Gene:
                          CYFIP1 (Varview), NIPA2 (Varview)
                          Functional Consequence:
                          3_prime_UTR_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          A=0.000996/14 (ALFA)
                          -=0.000998/5 (1000Genomes)
                          -=0.001069/150 (GnomAD)
                          -=0.001111/294 (TOPMED)
                          HGVS:
                          NC_000015.10:g.22868306_22868307del, NC_000015.9:g.23004762_23004763del, NG_054889.1:g.117601_117602del, NM_014608.6:c.*1722_*1723del, NM_014608.5:c.*1722_*1723del, NM_001287810.4:c.*1722_*1723del, NM_001287810.3:c.*1722_*1723del, NM_001324122.3:c.*1722_*1723del, NM_001324122.2:c.*1722_*1723del, NM_001324123.3:c.*1722_*1723del, NM_001324123.2:c.*1722_*1723del, NM_001324124.3:c.*1722_*1723del, NM_001324124.2:c.*1722_*1723del, NM_001324126.3:c.*1722_*1723del, NM_001324126.2:c.*1722_*1723del, NM_001324125.3:c.*1722_*1723del, NM_001324125.2:c.*1722_*1723del, NM_001033028.3:c.*1722_*1723del, NM_001033028.2:c.*1722_*1723del, NM_001324120.2:c.*1722_*1723del, NM_001324119.2:c.*1722_*1723del, NG_021303.1:g.34666_34667del, NM_030922.7:c.*1459_*1460del, NM_030922.6:c.*1459_*1460del, NM_001008860.3:c.*1459_*1460del, NM_001008860.2:c.*1459_*1460del, NM_001008892.3:c.*1459_*1460del, NM_001008892.2:c.*1459_*1460del, NM_001008894.3:c.*1459_*1460del, NM_001008894.2:c.*1459_*1460del, NM_001184889.2:c.*1459_*1460del, NM_001184889.1:c.*1459_*1460del, NM_001184888.2:c.*1459_*1460del, NM_001184888.1:c.*1459_*1460del, NW_021160017.1:g.3762386_3762387del, XM_005272548.4:c.*1459_*1460del, XM_005272548.3:c.*1459_*1460del, XM_005272548.2:c.*1459_*1460del, XM_005272548.1:c.*1459_*1460del, XM_005272553.6:c.*1459_*1460del, XM_005272553.5:c.*1459_*1460del, XM_005272553.4:c.*1459_*1460del, XM_005272553.3:c.*1459_*1460del, XM_005272553.2:c.*1459_*1460del, XM_005272553.1:c.*1459_*1460del, XM_011543878.4:c.*1459_*1460del, XM_011543878.3:c.*1459_*1460del, XM_011543878.2:c.*1459_*1460del, XM_011543878.1:c.*1459_*1460del, XM_005272546.4:c.*1459_*1460del, XM_005272546.3:c.*1459_*1460del, XM_005272546.2:c.*1459_*1460del, XM_005272546.1:c.*1459_*1460del, XM_005272547.5:c.*1459_*1460del, XM_005272547.4:c.*1459_*1460del, XM_005272547.3:c.*1459_*1460del, XM_005272547.2:c.*1459_*1460del, XM_005272547.1:c.*1459_*1460del, XM_005272552.5:c.*1459_*1460del, XM_005272552.4:c.*1459_*1460del, XM_005272552.3:c.*1459_*1460del, XM_005272552.2:c.*1459_*1460del, XM_005272552.1:c.*1459_*1460del, XM_011543880.4:c.*1459_*1460del, XM_011543880.3:c.*1459_*1460del, XM_011543880.2:c.*1459_*1460del, XM_011543880.1:c.*1459_*1460del, XM_005272550.4:c.*1459_*1460del, XM_005272550.3:c.*1459_*1460del, XM_005272550.2:c.*1459_*1460del, XM_005272550.1:c.*1459_*1460del, XM_011543879.4:c.*1459_*1460del, XM_011543879.3:c.*1459_*1460del, XM_011543879.2:c.*1459_*1460del, XM_011543879.1:c.*1459_*1460del, XM_017022651.3:c.*1459_*1460del, XM_017022651.2:c.*1459_*1460del, XM_017022651.1:c.*1459_*1460del, XM_017022653.3:c.*1459_*1460del, XM_017022653.2:c.*1459_*1460del, XM_017022653.1:c.*1459_*1460del, XM_011543877.3:c.*1459_*1460del, XM_011543877.2:c.*1459_*1460del, XM_011543877.1:c.*1459_*1460del, XM_017022649.3:c.*1459_*1460del, XM_017022649.2:c.*1459_*1460del, XM_017022649.1:c.*1459_*1460del, XM_017022650.3:c.*1459_*1460del, XM_017022650.2:c.*1459_*1460del, XM_017022650.1:c.*1459_*1460del, XM_006720364.3:c.*1459_*1460del, XM_006720364.2:c.*1459_*1460del, XM_006720364.1:c.*1459_*1460del, XM_017022652.3:c.*1459_*1460del, XM_017022652.2:c.*1459_*1460del, XM_017022652.1:c.*1459_*1460del, XM_017022654.3:c.*1459_*1460del, XM_017022654.2:c.*1459_*1460del, XM_017022654.1:c.*1459_*1460del, XM_017022645.2:c.*1459_*1460del, XM_017022645.1:c.*1459_*1460del, XM_017022648.2:c.*1459_*1460del, XM_017022648.1:c.*1459_*1460del, XM_006720367.2:c.*1459_*1460del, XM_006720367.1:c.*1459_*1460del, XM_017022646.2:c.*1459_*1460del, XM_017022646.1:c.*1459_*1460del, XM_017022647.2:c.*1459_*1460del, XM_017022647.1:c.*1459_*1460del, XM_017022660.2:c.*1459_*1460del, XM_017022660.1:c.*1459_*1460del, XM_017022657.2:c.*1459_*1460del, XM_017022657.1:c.*1459_*1460del, XM_017022659.2:c.*1459_*1460del, XM_017022659.1:c.*1459_*1460del, XM_017022655.2:c.*1459_*1460del, XM_017022655.1:c.*1459_*1460del, XM_017022662.2:c.*1459_*1460del, XM_017022662.1:c.*1459_*1460del, XM_017022661.2:c.*1459_*1460del, XM_017022661.1:c.*1459_*1460del, XM_017022658.2:c.*1459_*1460del, XM_017022658.1:c.*1459_*1460del, XM_017022663.2:c.*1459_*1460del, XM_017022663.1:c.*1459_*1460del, XM_047433159.1:c.*1459_*1460del, XM_017022656.2:c.*1459_*1460del, XM_017022656.1:c.*1459_*1460del, XM_047433158.1:c.*1459_*1460del, XM_047433153.1:c.*1459_*1460del, XM_047433163.1:c.*1459_*1460del, XM_047433154.1:c.*1459_*1460del, XM_047433152.1:c.*1459_*1460del, XM_047433156.1:c.*1459_*1460del, XM_047433150.1:c.*1459_*1460del, XM_047433151.1:c.*1459_*1460del, XM_047433162.1:c.*1459_*1460del, XM_047433160.1:c.*1459_*1460del, XM_047433157.1:c.*1459_*1460del, XM_047433161.1:c.*1459_*1460del, XM_047433155.1:c.*1459_*1460del

                          13.

                          rs1491019226 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            ->TT [Show Flanks]
                            Chromosome:
                            15:22868624 (GRCh38)
                            15:23004442 (GRCh37)
                            Canonical SPDI:
                            NC_000015.10:22868624:TT:TTTT
                            Gene:
                            CYFIP1 (Varview), NIPA2 (Varview)
                            Functional Consequence:
                            3_prime_UTR_variant,downstream_transcript_variant,500B_downstream_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            TTTT=0./0 (ALFA)
                            TT=0.000007/1 (GnomAD)
                            TT=0.000015/4 (TOPMED)
                            AA=0.000597/10 (TOMMO)
                            HGVS:

                            14.

                            rs1490965509 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              C>G [Show Flanks]
                              Chromosome:
                              15:22870123 (GRCh38)
                              15:23002945 (GRCh37)
                              Canonical SPDI:
                              NC_000015.10:22870122:C:G
                              Gene:
                              CYFIP1 (Varview)
                              Functional Consequence:
                              missense_variant,coding_sequence_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              G=0./0 (ALFA)
                              G=0.000004/1 (TOPMED)
                              G=0.000007/1 (GnomAD)
                              HGVS:
                              NC_000015.10:g.22870123C>G, NC_000015.9:g.23002945G>C, NG_054889.1:g.115784G>C, NM_014608.6:c.3667G>C, NM_014608.5:c.3667G>C, NM_014608.4:c.3667G>C, NM_014608.3:c.3667G>C, NM_014608.2:c.3667G>C, NM_001287810.4:c.3667G>C, NM_001287810.3:c.3667G>C, NM_001287810.2:c.3667G>C, NM_001287810.1:c.3667G>C, NM_001324122.3:c.1987G>C, NM_001324122.2:c.1987G>C, NM_001324122.1:c.1987G>C, NM_001324123.3:c.3667G>C, NM_001324123.2:c.3667G>C, NM_001324123.1:c.3667G>C, NM_001324124.3:c.3577G>C, NM_001324124.2:c.3577G>C, NM_001324124.1:c.3577G>C, NM_001324126.3:c.3565G>C, NM_001324126.2:c.3565G>C, NM_001324126.1:c.3565G>C, NM_001324125.3:c.3301G>C, NM_001324125.2:c.3301G>C, NM_001324125.1:c.3301G>C, NM_001033028.3:c.2374G>C, NM_001033028.2:c.2374G>C, NM_001033028.1:c.2374G>C, NM_001324120.2:c.3667G>C, NM_001324120.1:c.3667G>C, NM_001324119.2:c.3769G>C, NM_001324119.1:c.3769G>C, NG_021303.1:g.36483C>G, NW_021160017.1:g.3764199C>G, NP_055423.1:p.Asp1223His, NP_001274739.1:p.Asp1223His, NP_001311051.1:p.Asp663His, NP_001311052.1:p.Asp1223His, NP_001311053.1:p.Asp1193His, NP_001311055.1:p.Asp1189His, NP_001311054.1:p.Asp1101His, NP_001028200.1:p.Asp792His, NP_001311049.1:p.Asp1223His, NP_001311048.1:p.Asp1257His

                              15.

                              rs1490940258 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                G>T [Show Flanks]
                                Chromosome:
                                15:22869456 (GRCh38)
                                15:23003612 (GRCh37)
                                Canonical SPDI:
                                NC_000015.10:22869455:G:T
                                Gene:
                                CYFIP1 (Varview)
                                Functional Consequence:
                                3_prime_UTR_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                T=0./0 (ALFA)
                                HGVS:

                                16.

                                rs1490166991 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>A [Show Flanks]
                                  Chromosome:
                                  15:22932235 (GRCh38)
                                  15:22940833 (GRCh37)
                                  Canonical SPDI:
                                  NC_000015.10:22932234:G:A
                                  Gene:
                                  CYFIP1 (Varview)
                                  Functional Consequence:
                                  5_prime_UTR_variant,genic_upstream_transcript_variant,coding_sequence_variant,synonymous_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  A=0.000028/1 (ALFA)
                                  T=0.000004/1 (GnomAD_exomes)
                                  A=0.000015/4 (TOPMED)
                                  HGVS:
                                  NC_000015.10:g.22932235G>A, NC_000015.9:g.22940833C>T, NG_054889.1:g.53672C>T, NM_014608.6:c.1098C>T, NM_014608.5:c.1098C>T, NM_014608.4:c.1098C>T, NM_014608.3:c.1098C>T, NM_014608.2:c.1098C>T, NM_001287810.4:c.1098C>T, NM_001287810.3:c.1098C>T, NM_001287810.2:c.1098C>T, NM_001287810.1:c.1098C>T, NM_001324122.3:c.-731C>T, NM_001324122.2:c.-731C>T, NM_001324122.1:c.-731C>T, NM_001324123.3:c.1098C>T, NM_001324123.2:c.1098C>T, NM_001324123.1:c.1098C>T, NM_001324124.3:c.1008C>T, NM_001324124.2:c.1008C>T, NM_001324124.1:c.1008C>T, NM_001324126.3:c.996C>T, NM_001324126.2:c.996C>T, NM_001324126.1:c.996C>T, NM_001324125.3:c.732C>T, NM_001324125.2:c.732C>T, NM_001324125.1:c.732C>T, NM_001324120.2:c.1098C>T, NM_001324120.1:c.1098C>T, NM_001324119.2:c.1200C>T, NM_001324119.1:c.1200C>T, NW_021160017.1:g.3826320G>A, NT_187603.1:g.29264G>A

                                  17.

                                  rs1489986504 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    A>G [Show Flanks]
                                    Chromosome:
                                    15:22869527 (GRCh38)
                                    15:23003541 (GRCh37)
                                    Canonical SPDI:
                                    NC_000015.10:22869526:A:G
                                    Gene:
                                    CYFIP1 (Varview)
                                    Functional Consequence:
                                    3_prime_UTR_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    G=0./0 (ALFA)
                                    G=0.000008/2 (TOPMED)
                                    G=0.000014/2 (GnomAD)
                                    HGVS:
                                    NC_000015.10:g.22869527A>G, NC_000015.9:g.23003541T>C, NG_054889.1:g.116380T>C, NM_014608.6:c.*501T>C, NM_014608.5:c.*501T>C, NM_014608.4:c.*501T>C, NM_014608.3:c.*501T>C, NM_014608.2:c.*501T>C, NM_001287810.4:c.*501T>C, NM_001287810.3:c.*501T>C, NM_001287810.2:c.*501T>C, NM_001287810.1:c.*501T>C, NM_001324122.3:c.*501T>C, NM_001324122.2:c.*501T>C, NM_001324122.1:c.*501T>C, NM_001324123.3:c.*501T>C, NM_001324123.2:c.*501T>C, NM_001324123.1:c.*501T>C, NM_001324124.3:c.*501T>C, NM_001324124.2:c.*501T>C, NM_001324124.1:c.*501T>C, NM_001324126.3:c.*501T>C, NM_001324126.2:c.*501T>C, NM_001324126.1:c.*501T>C, NM_001324125.3:c.*501T>C, NM_001324125.2:c.*501T>C, NM_001324125.1:c.*501T>C, NM_001033028.3:c.*501T>C, NM_001033028.2:c.*501T>C, NM_001033028.1:c.*501T>C, NM_001324120.2:c.*501T>C, NM_001324120.1:c.*501T>C, NM_001324119.2:c.*501T>C, NM_001324119.1:c.*501T>C, NG_021303.1:g.35887A>G, NW_021160017.1:g.3763603A>G

                                    18.

                                    rs1489960384 [Homo sapiens]
                                      Variant type:
                                      DELINS
                                      Alleles:
                                      ->CTTT [Show Flanks]
                                      Chromosome:
                                      15:22868921 (GRCh38)
                                      15:23004142 (GRCh37)
                                      Canonical SPDI:
                                      NC_000015.10:22868921:TCTTT:TCTTTCTTT
                                      Gene:
                                      CYFIP1 (Varview)
                                      Functional Consequence:
                                      3_prime_UTR_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      TCTTTCTTT=0.000071/1 (ALFA)
                                      TCTT=0./0 (GnomAD)
                                      TCTT=0.000015/4 (TOPMED)
                                      HGVS:

                                      19.

                                      rs1488388549 [Homo sapiens]
                                        Variant type:
                                        DELINS
                                        Alleles:
                                        ->CTTTG [Show Flanks]
                                        Chromosome:
                                        15:22868289 (GRCh38)
                                        15:23004772 (GRCh37)
                                        Canonical SPDI:
                                        NC_000015.10:22868289:TGCTTTG:TGCTTTGCTTTG
                                        Gene:
                                        CYFIP1 (Varview), NIPA2 (Varview)
                                        Functional Consequence:
                                        3_prime_UTR_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        TGCTTTGCTTTG=0.000071/1 (ALFA)
                                        TGCTT=0.000034/9 (TOPMED)
                                        TGCTT=0.000036/5 (GnomAD)
                                        HGVS:
                                        NC_000015.10:g.22868292_22868296dup, NC_000015.9:g.23004774_23004778dup, NG_054889.1:g.117613_117617dup, NM_014608.6:c.*1734_*1738dup, NM_014608.5:c.*1734_*1738dup, NM_001287810.4:c.*1734_*1738dup, NM_001287810.3:c.*1734_*1738dup, NM_001324122.3:c.*1734_*1738dup, NM_001324122.2:c.*1734_*1738dup, NM_001324123.3:c.*1734_*1738dup, NM_001324123.2:c.*1734_*1738dup, NM_001324124.3:c.*1734_*1738dup, NM_001324124.2:c.*1734_*1738dup, NM_001324126.3:c.*1734_*1738dup, NM_001324126.2:c.*1734_*1738dup, NM_001324125.3:c.*1734_*1738dup, NM_001324125.2:c.*1734_*1738dup, NM_001033028.3:c.*1734_*1738dup, NM_001033028.2:c.*1734_*1738dup, NM_001324120.2:c.*1734_*1738dup, NM_001324119.2:c.*1734_*1738dup, NG_021303.1:g.34652_34656dup, NM_030922.7:c.*1445_*1449dup, NM_030922.6:c.*1445_*1449dup, NM_001008860.3:c.*1445_*1449dup, NM_001008860.2:c.*1445_*1449dup, NM_001008892.3:c.*1445_*1449dup, NM_001008892.2:c.*1445_*1449dup, NM_001008894.3:c.*1445_*1449dup, NM_001008894.2:c.*1445_*1449dup, NM_001184889.2:c.*1445_*1449dup, NM_001184889.1:c.*1445_*1449dup, NM_001184888.2:c.*1445_*1449dup, NM_001184888.1:c.*1445_*1449dup, NW_021160017.1:g.3762372_3762376dup, XM_005272548.4:c.*1445_*1449dup, XM_005272548.3:c.*1445_*1449dup, XM_005272548.2:c.*1445_*1449dup, XM_005272548.1:c.*1445_*1449dup, XM_005272553.6:c.*1445_*1449dup, XM_005272553.5:c.*1445_*1449dup, XM_005272553.4:c.*1445_*1449dup, XM_005272553.3:c.*1445_*1449dup, XM_005272553.2:c.*1445_*1449dup, XM_005272553.1:c.*1445_*1449dup, XM_011543878.4:c.*1445_*1449dup, XM_011543878.3:c.*1445_*1449dup, XM_011543878.2:c.*1445_*1449dup, XM_011543878.1:c.*1445_*1449dup, XM_005272546.4:c.*1445_*1449dup, XM_005272546.3:c.*1445_*1449dup, XM_005272546.2:c.*1445_*1449dup, XM_005272546.1:c.*1445_*1449dup, XM_005272547.5:c.*1445_*1449dup, XM_005272547.4:c.*1445_*1449dup, XM_005272547.3:c.*1445_*1449dup, XM_005272547.2:c.*1445_*1449dup, XM_005272547.1:c.*1445_*1449dup, XM_005272552.5:c.*1445_*1449dup, XM_005272552.4:c.*1445_*1449dup, XM_005272552.3:c.*1445_*1449dup, XM_005272552.2:c.*1445_*1449dup, XM_005272552.1:c.*1445_*1449dup, XM_011543880.4:c.*1445_*1449dup, XM_011543880.3:c.*1445_*1449dup, XM_011543880.2:c.*1445_*1449dup, XM_011543880.1:c.*1445_*1449dup, XM_005272550.4:c.*1445_*1449dup, XM_005272550.3:c.*1445_*1449dup, XM_005272550.2:c.*1445_*1449dup, XM_005272550.1:c.*1445_*1449dup, XM_011543879.4:c.*1445_*1449dup, XM_011543879.3:c.*1445_*1449dup, XM_011543879.2:c.*1445_*1449dup, XM_011543879.1:c.*1445_*1449dup, XM_017022651.3:c.*1445_*1449dup, XM_017022651.2:c.*1445_*1449dup, XM_017022651.1:c.*1445_*1449dup, XM_017022653.3:c.*1445_*1449dup, XM_017022653.2:c.*1445_*1449dup, XM_017022653.1:c.*1445_*1449dup, XM_011543877.3:c.*1445_*1449dup, XM_011543877.2:c.*1445_*1449dup, XM_011543877.1:c.*1445_*1449dup, XM_017022649.3:c.*1445_*1449dup, XM_017022649.2:c.*1445_*1449dup, XM_017022649.1:c.*1445_*1449dup, XM_017022650.3:c.*1445_*1449dup, XM_017022650.2:c.*1445_*1449dup, XM_017022650.1:c.*1445_*1449dup, XM_006720364.3:c.*1445_*1449dup, XM_006720364.2:c.*1445_*1449dup, XM_006720364.1:c.*1445_*1449dup, XM_017022652.3:c.*1445_*1449dup, XM_017022652.2:c.*1445_*1449dup, XM_017022652.1:c.*1445_*1449dup, XM_017022654.3:c.*1445_*1449dup, XM_017022654.2:c.*1445_*1449dup, XM_017022654.1:c.*1445_*1449dup, XM_017022645.2:c.*1445_*1449dup, XM_017022645.1:c.*1445_*1449dup, XM_017022646.2:c.*1445_*1449dup, XM_017022646.1:c.*1445_*1449dup, XM_017022647.2:c.*1445_*1449dup, XM_017022647.1:c.*1445_*1449dup, XM_017022660.2:c.*1445_*1449dup, XM_017022660.1:c.*1445_*1449dup, XM_017022657.2:c.*1445_*1449dup, XM_017022657.1:c.*1445_*1449dup, XM_017022659.2:c.*1445_*1449dup, XM_017022659.1:c.*1445_*1449dup, XM_017022656.2:c.*1445_*1449dup, XM_017022656.1:c.*1445_*1449dup, XM_017022655.2:c.*1445_*1449dup, XM_017022655.1:c.*1445_*1449dup, XM_017022662.2:c.*1445_*1449dup, XM_017022662.1:c.*1445_*1449dup, XM_017022661.2:c.*1445_*1449dup, XM_017022661.1:c.*1445_*1449dup, XM_017022658.2:c.*1445_*1449dup, XM_017022658.1:c.*1445_*1449dup, XM_017022663.2:c.*1445_*1449dup, XM_017022663.1:c.*1445_*1449dup, XM_017022648.2:c.*1445_*1449dup, XM_017022648.1:c.*1445_*1449dup, XM_006720367.2:c.*1445_*1449dup, XM_006720367.1:c.*1445_*1449dup, XM_047433156.1:c.*1445_*1449dup, XM_047433150.1:c.*1445_*1449dup, XM_047433155.1:c.*1445_*1449dup, XM_047433158.1:c.*1445_*1449dup, XM_047433151.1:c.*1445_*1449dup, XM_047433162.1:c.*1445_*1449dup, XM_047433154.1:c.*1445_*1449dup, XM_047433157.1:c.*1445_*1449dup, XM_047433153.1:c.*1445_*1449dup, XM_047433163.1:c.*1445_*1449dup, XM_047433152.1:c.*1445_*1449dup, XM_047433161.1:c.*1445_*1449dup, XM_047433159.1:c.*1445_*1449dup, XM_047433160.1:c.*1445_*1449dup

                                        20.

                                        rs1488198336 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          C>A [Show Flanks]
                                          Chromosome:
                                          15:22868524 (GRCh38)
                                          15:23004544 (GRCh37)
                                          Canonical SPDI:
                                          NC_000015.10:22868523:C:A
                                          Gene:
                                          CYFIP1 (Varview), NIPA2 (Varview)
                                          Functional Consequence:
                                          3_prime_UTR_variant,downstream_transcript_variant,500B_downstream_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          A=0./0 (ALFA)
                                          A=0.000019/5 (TOPMED)
                                          HGVS:

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