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Items: 1 to 20 of 14034

1.

rs1491586785 has merged into rs763370326 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    TT>-,T,TTT [Show Flanks]
    Chromosome:
    Y:2714411 (GRCh38)
    Y:2582452 (GRCh37)
    Canonical SPDI:
    NC_000024.10:2714405:TTTTTTT:TTTTT,NC_000024.10:2714405:TTTTTTT:TTTTTT,NC_000024.10:2714405:TTTTTTT:TTTTTTTT
    Gene:
    CD99 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    TTTTTTTT=0./0 (ALFA)
    -=0.000016/2 (ExAC)
    -=0.000021/5 (GnomAD_exomes)
    HGVS:

    2.

    rs1491528630 [Homo sapiens]
      Variant type:
      DEL
      Alleles:
      CA>- [Show Flanks]
      Chromosome:
      Y:2730929 (GRCh38)
      Y:2598970 (GRCh37)
      Canonical SPDI:
      NC_000024.10:2730928:CA:
      Gene:
      CD99 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa
      MAF:
      -=0.00034/4 (ALFA)
      -=0.00085/24 (TOMMO)
      HGVS:

      3.

      rs1491493304 [Homo sapiens]
        Variant type:
        DEL
        Alleles:
        CT>- [Show Flanks]
        Chromosome:
        Y:2688381 (GRCh38)
        Y:2556422 (GRCh37)
        Canonical SPDI:
        NC_000024.10:2688380:CT:
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        -=0.000506/6 (ALFA)
        -=0.00106/111 (GnomAD)
        HGVS:

        4.

        rs1491456414 [Homo sapiens]
          Variant type:
          INS
          Alleles:
          ->TTA [Show Flanks]
          Chromosome:
          Y:2688398 (GRCh38)
          Y:2556440 (GRCh37)
          Canonical SPDI:
          NC_000024.10:2688398::TTA
          HGVS:

          5.

          rs1491261098 has merged into rs66911350 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTTT [Show Flanks]
            Chromosome:
            Y:2742034 (GRCh38)
            Y:2610075 (GRCh37)
            Canonical SPDI:
            NC_000024.10:2742019:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000024.10:2742019:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000024.10:2742019:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000024.10:2742019:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000024.10:2742019:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000024.10:2742019:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742019:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            TTTTTTTTTTTTTTTT=0./0 (ALFA)
            HGVS:
            NC_000024.10:g.2742034_2742037del, NC_000024.10:g.2742035_2742037del, NC_000024.10:g.2742036_2742037del, NC_000024.10:g.2742037del, NC_000024.10:g.2742037dup, NC_000024.10:g.2742036_2742037dup, NC_000024.10:g.2742034_2742037dup, NC_000024.9:g.2610075_2610078del, NC_000024.9:g.2610076_2610078del, NC_000024.9:g.2610077_2610078del, NC_000024.9:g.2610078del, NC_000024.9:g.2610078dup, NC_000024.9:g.2610077_2610078dup, NC_000024.9:g.2610075_2610078dup, NG_009174.1:g.55848_55851del, NG_009174.1:g.55849_55851del, NG_009174.1:g.55850_55851del, NG_009174.1:g.55851del, NG_009174.1:g.55851dup, NG_009174.1:g.55850_55851dup, NG_009174.1:g.55848_55851dup, NC_000023.11:g.2742034_2742037del, NC_000023.11:g.2742035_2742037del, NC_000023.11:g.2742036_2742037del, NC_000023.11:g.2742037del, NC_000023.11:g.2742037dup, NC_000023.11:g.2742036_2742037dup, NC_000023.11:g.2742034_2742037dup, NC_000023.10:g.2660075_2660078del, NC_000023.10:g.2660076_2660078del, NC_000023.10:g.2660077_2660078del, NC_000023.10:g.2660078del, NC_000023.10:g.2660078dup, NC_000023.10:g.2660077_2660078dup, NC_000023.10:g.2660075_2660078dup

            6.

            rs1491239248 has merged into rs556444956 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT>-,GT,GTGT,GTGTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT [Show Flanks]
              Chromosome:
              Y:2703620 (GRCh38)
              Y:2571661 (GRCh37)
              Canonical SPDI:
              NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000024.10:2703605:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
              Gene:
              CD99 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              GTGTGTGTGTGTGT=0./0 (ALFA)
              HGVS:
              NC_000024.10:g.2703606GT[7], NC_000024.10:g.2703606GT[8], NC_000024.10:g.2703606GT[9], NC_000024.10:g.2703606GT[10], NC_000024.10:g.2703606GT[11], NC_000024.10:g.2703606GT[12], NC_000024.10:g.2703606GT[13], NC_000024.10:g.2703606GT[14], NC_000024.10:g.2703606GT[15], NC_000024.10:g.2703606GT[16], NC_000024.10:g.2703606GT[17], NC_000024.10:g.2703606GT[18], NC_000024.10:g.2703606GT[19], NC_000024.10:g.2703606GT[20], NC_000024.10:g.2703606GT[21], NC_000024.10:g.2703606GT[22], NC_000024.10:g.2703606GT[24], NC_000024.10:g.2703606GT[25], NC_000024.10:g.2703606GT[26], NC_000024.10:g.2703606GT[27], NC_000024.10:g.2703606GT[28], NC_000024.10:g.2703606GT[29], NC_000024.10:g.2703606GT[30], NC_000024.10:g.2703606GT[31], NC_000024.10:g.2703606GT[32], NC_000024.10:g.2703606GT[33], NC_000024.10:g.2703606GT[34], NC_000024.9:g.2571647GT[7], NC_000024.9:g.2571647GT[8], NC_000024.9:g.2571647GT[9], NC_000024.9:g.2571647GT[10], NC_000024.9:g.2571647GT[11], NC_000024.9:g.2571647GT[12], NC_000024.9:g.2571647GT[13], NC_000024.9:g.2571647GT[14], NC_000024.9:g.2571647GT[15], NC_000024.9:g.2571647GT[16], NC_000024.9:g.2571647GT[17], NC_000024.9:g.2571647GT[18], NC_000024.9:g.2571647GT[19], NC_000024.9:g.2571647GT[20], NC_000024.9:g.2571647GT[21], NC_000024.9:g.2571647GT[22], NC_000024.9:g.2571647GT[24], NC_000024.9:g.2571647GT[25], NC_000024.9:g.2571647GT[26], NC_000024.9:g.2571647GT[27], NC_000024.9:g.2571647GT[28], NC_000024.9:g.2571647GT[29], NC_000024.9:g.2571647GT[30], NC_000024.9:g.2571647GT[31], NC_000024.9:g.2571647GT[32], NC_000024.9:g.2571647GT[33], NC_000024.9:g.2571647GT[34], NG_009174.1:g.17420GT[7], NG_009174.1:g.17420GT[8], NG_009174.1:g.17420GT[9], NG_009174.1:g.17420GT[10], NG_009174.1:g.17420GT[11], NG_009174.1:g.17420GT[12], NG_009174.1:g.17420GT[13], NG_009174.1:g.17420GT[14], NG_009174.1:g.17420GT[15], NG_009174.1:g.17420GT[16], NG_009174.1:g.17420GT[17], NG_009174.1:g.17420GT[18], NG_009174.1:g.17420GT[19], NG_009174.1:g.17420GT[20], NG_009174.1:g.17420GT[21], NG_009174.1:g.17420GT[22], NG_009174.1:g.17420GT[24], NG_009174.1:g.17420GT[25], NG_009174.1:g.17420GT[26], NG_009174.1:g.17420GT[27], NG_009174.1:g.17420GT[28], NG_009174.1:g.17420GT[29], NG_009174.1:g.17420GT[30], NG_009174.1:g.17420GT[31], NG_009174.1:g.17420GT[32], NG_009174.1:g.17420GT[33], NG_009174.1:g.17420GT[34], NC_000023.11:g.2703606GT[7], NC_000023.11:g.2703606GT[8], NC_000023.11:g.2703606GT[9], NC_000023.11:g.2703606GT[10], NC_000023.11:g.2703606GT[11], NC_000023.11:g.2703606GT[12], NC_000023.11:g.2703606GT[13], NC_000023.11:g.2703606GT[14], NC_000023.11:g.2703606GT[15], NC_000023.11:g.2703606GT[16], NC_000023.11:g.2703606GT[17], NC_000023.11:g.2703606GT[18], NC_000023.11:g.2703606GT[19], NC_000023.11:g.2703606GT[20], NC_000023.11:g.2703606GT[21], NC_000023.11:g.2703606GT[22], NC_000023.11:g.2703606GT[24], NC_000023.11:g.2703606GT[25], NC_000023.11:g.2703606GT[26], NC_000023.11:g.2703606GT[27], NC_000023.11:g.2703606GT[28], NC_000023.11:g.2703606GT[29], NC_000023.11:g.2703606GT[30], NC_000023.11:g.2703606GT[31], NC_000023.11:g.2703606GT[32], NC_000023.11:g.2703606GT[33], NC_000023.11:g.2703606GT[34], NC_000023.10:g.2621647GT[7], NC_000023.10:g.2621647GT[8], NC_000023.10:g.2621647GT[9], NC_000023.10:g.2621647GT[10], NC_000023.10:g.2621647GT[11], NC_000023.10:g.2621647GT[12], NC_000023.10:g.2621647GT[13], NC_000023.10:g.2621647GT[14], NC_000023.10:g.2621647GT[15], NC_000023.10:g.2621647GT[16], NC_000023.10:g.2621647GT[17], NC_000023.10:g.2621647GT[18], NC_000023.10:g.2621647GT[19], NC_000023.10:g.2621647GT[20], NC_000023.10:g.2621647GT[21], NC_000023.10:g.2621647GT[22], NC_000023.10:g.2621647GT[24], NC_000023.10:g.2621647GT[25], NC_000023.10:g.2621647GT[26], NC_000023.10:g.2621647GT[27], NC_000023.10:g.2621647GT[28], NC_000023.10:g.2621647GT[29], NC_000023.10:g.2621647GT[30], NC_000023.10:g.2621647GT[31], NC_000023.10:g.2621647GT[32], NC_000023.10:g.2621647GT[33], NC_000023.10:g.2621647GT[34]

              7.

              rs1491236184 has merged into rs1158289378 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                TTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                Chromosome:
                Y:2742654 (GRCh38)
                Y:2610695 (GRCh37)
                Canonical SPDI:
                NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000024.10:2742640:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                TTTTTTTTTTTTT=0./0 (ALFA)
                HGVS:
                NC_000024.10:g.2742654_2742671del, NC_000024.10:g.2742655_2742671del, NC_000024.10:g.2742656_2742671del, NC_000024.10:g.2742657_2742671del, NC_000024.10:g.2742658_2742671del, NC_000024.10:g.2742659_2742671del, NC_000024.10:g.2742660_2742671del, NC_000024.10:g.2742661_2742671del, NC_000024.10:g.2742662_2742671del, NC_000024.10:g.2742663_2742671del, NC_000024.10:g.2742664_2742671del, NC_000024.10:g.2742665_2742671del, NC_000024.10:g.2742666_2742671del, NC_000024.10:g.2742667_2742671del, NC_000024.10:g.2742668_2742671del, NC_000024.10:g.2742669_2742671del, NC_000024.10:g.2742670_2742671del, NC_000024.10:g.2742671del, NC_000024.10:g.2742671dup, NC_000024.10:g.2742670_2742671dup, NC_000024.10:g.2742641_2742671T[33]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000024.10:g.2742669_2742671dup, NC_000024.10:g.2742668_2742671dup, NC_000024.10:g.2742667_2742671dup, NC_000024.10:g.2742666_2742671dup, NC_000024.10:g.2742665_2742671dup, NC_000024.10:g.2742664_2742671dup, NC_000024.10:g.2742663_2742671dup, NC_000024.10:g.2742662_2742671dup, NC_000024.10:g.2742661_2742671dup, NC_000024.10:g.2742660_2742671dup, NC_000024.10:g.2742659_2742671dup, NC_000024.10:g.2742658_2742671dup, NC_000024.10:g.2742656_2742671dup, NC_000024.10:g.2742655_2742671dup, NC_000024.10:g.2742654_2742671dup, NC_000024.10:g.2742653_2742671dup, NC_000024.10:g.2742643_2742671dup, NC_000024.10:g.2742642_2742671dup, NC_000024.10:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.10:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.10:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.10:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.10:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.10:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.10:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.10:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.10:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.10:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.10:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.10:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.9:g.2610695_2610712del, NC_000024.9:g.2610696_2610712del, NC_000024.9:g.2610697_2610712del, NC_000024.9:g.2610698_2610712del, NC_000024.9:g.2610699_2610712del, NC_000024.9:g.2610700_2610712del, NC_000024.9:g.2610701_2610712del, NC_000024.9:g.2610702_2610712del, NC_000024.9:g.2610703_2610712del, NC_000024.9:g.2610704_2610712del, NC_000024.9:g.2610705_2610712del, NC_000024.9:g.2610706_2610712del, NC_000024.9:g.2610707_2610712del, NC_000024.9:g.2610708_2610712del, NC_000024.9:g.2610709_2610712del, NC_000024.9:g.2610710_2610712del, NC_000024.9:g.2610711_2610712del, NC_000024.9:g.2610712del, NC_000024.9:g.2610712dup, NC_000024.9:g.2610711_2610712dup, NC_000024.9:g.2610682_2610712T[33]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000024.9:g.2610710_2610712dup, NC_000024.9:g.2610709_2610712dup, NC_000024.9:g.2610708_2610712dup, NC_000024.9:g.2610707_2610712dup, NC_000024.9:g.2610706_2610712dup, NC_000024.9:g.2610705_2610712dup, NC_000024.9:g.2610704_2610712dup, NC_000024.9:g.2610703_2610712dup, NC_000024.9:g.2610702_2610712dup, NC_000024.9:g.2610701_2610712dup, NC_000024.9:g.2610700_2610712dup, NC_000024.9:g.2610699_2610712dup, NC_000024.9:g.2610697_2610712dup, NC_000024.9:g.2610696_2610712dup, NC_000024.9:g.2610695_2610712dup, NC_000024.9:g.2610694_2610712dup, NC_000024.9:g.2610684_2610712dup, NC_000024.9:g.2610683_2610712dup, NC_000024.9:g.2610712_2610713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.9:g.2610712_2610713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.9:g.2610712_2610713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.9:g.2610712_2610713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.9:g.2610712_2610713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.9:g.2610712_2610713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.9:g.2610712_2610713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.9:g.2610712_2610713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.9:g.2610712_2610713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.9:g.2610712_2610713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.9:g.2610712_2610713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000024.9:g.2610712_2610713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_009174.1:g.56468_56485del, NG_009174.1:g.56469_56485del, NG_009174.1:g.56470_56485del, NG_009174.1:g.56471_56485del, NG_009174.1:g.56472_56485del, NG_009174.1:g.56473_56485del, NG_009174.1:g.56474_56485del, NG_009174.1:g.56475_56485del, NG_009174.1:g.56476_56485del, NG_009174.1:g.56477_56485del, NG_009174.1:g.56478_56485del, NG_009174.1:g.56479_56485del, NG_009174.1:g.56480_56485del, NG_009174.1:g.56481_56485del, NG_009174.1:g.56482_56485del, NG_009174.1:g.56483_56485del, NG_009174.1:g.56484_56485del, NG_009174.1:g.56485del, NG_009174.1:g.56485dup, NG_009174.1:g.56484_56485dup, NG_009174.1:g.56455_56485T[33]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_009174.1:g.56483_56485dup, NG_009174.1:g.56482_56485dup, NG_009174.1:g.56481_56485dup, NG_009174.1:g.56480_56485dup, NG_009174.1:g.56479_56485dup, NG_009174.1:g.56478_56485dup, NG_009174.1:g.56477_56485dup, NG_009174.1:g.56476_56485dup, NG_009174.1:g.56475_56485dup, NG_009174.1:g.56474_56485dup, NG_009174.1:g.56473_56485dup, NG_009174.1:g.56472_56485dup, NG_009174.1:g.56470_56485dup, NG_009174.1:g.56469_56485dup, NG_009174.1:g.56468_56485dup, NG_009174.1:g.56467_56485dup, NG_009174.1:g.56457_56485dup, NG_009174.1:g.56456_56485dup, NG_009174.1:g.56485_56486insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_009174.1:g.56485_56486insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_009174.1:g.56485_56486insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_009174.1:g.56485_56486insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_009174.1:g.56485_56486insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_009174.1:g.56485_56486insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_009174.1:g.56485_56486insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_009174.1:g.56485_56486insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_009174.1:g.56485_56486insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_009174.1:g.56485_56486insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_009174.1:g.56485_56486insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_009174.1:g.56485_56486insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.11:g.2742654_2742671del, NC_000023.11:g.2742655_2742671del, NC_000023.11:g.2742656_2742671del, NC_000023.11:g.2742657_2742671del, NC_000023.11:g.2742658_2742671del, NC_000023.11:g.2742659_2742671del, NC_000023.11:g.2742660_2742671del, NC_000023.11:g.2742661_2742671del, NC_000023.11:g.2742662_2742671del, NC_000023.11:g.2742663_2742671del, NC_000023.11:g.2742664_2742671del, NC_000023.11:g.2742665_2742671del, NC_000023.11:g.2742666_2742671del, NC_000023.11:g.2742667_2742671del, NC_000023.11:g.2742668_2742671del, NC_000023.11:g.2742669_2742671del, NC_000023.11:g.2742670_2742671del, NC_000023.11:g.2742671del, NC_000023.11:g.2742671dup, NC_000023.11:g.2742670_2742671dup, NC_000023.11:g.2742641_2742671T[33]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000023.11:g.2742669_2742671dup, NC_000023.11:g.2742668_2742671dup, NC_000023.11:g.2742667_2742671dup, NC_000023.11:g.2742666_2742671dup, NC_000023.11:g.2742665_2742671dup, NC_000023.11:g.2742664_2742671dup, NC_000023.11:g.2742663_2742671dup, NC_000023.11:g.2742662_2742671dup, NC_000023.11:g.2742661_2742671dup, NC_000023.11:g.2742660_2742671dup, NC_000023.11:g.2742659_2742671dup, NC_000023.11:g.2742658_2742671dup, NC_000023.11:g.2742656_2742671dup, NC_000023.11:g.2742655_2742671dup, NC_000023.11:g.2742654_2742671dup, NC_000023.11:g.2742653_2742671dup, NC_000023.11:g.2742643_2742671dup, NC_000023.11:g.2742642_2742671dup, NC_000023.11:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.11:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.11:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.11:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.11:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.11:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.11:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.11:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.11:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.11:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.11:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.11:g.2742671_2742672insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.2660695_2660712del, NC_000023.10:g.2660696_2660712del, NC_000023.10:g.2660697_2660712del, NC_000023.10:g.2660698_2660712del, NC_000023.10:g.2660699_2660712del, NC_000023.10:g.2660700_2660712del, NC_000023.10:g.2660701_2660712del, NC_000023.10:g.2660702_2660712del, NC_000023.10:g.2660703_2660712del, NC_000023.10:g.2660704_2660712del, NC_000023.10:g.2660705_2660712del, NC_000023.10:g.2660706_2660712del, NC_000023.10:g.2660707_2660712del, NC_000023.10:g.2660708_2660712del, NC_000023.10:g.2660709_2660712del, NC_000023.10:g.2660710_2660712del, NC_000023.10:g.2660711_2660712del, NC_000023.10:g.2660712del, NC_000023.10:g.2660712dup, NC_000023.10:g.2660711_2660712dup, NC_000023.10:g.2660682_2660712T[33]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000023.10:g.2660710_2660712dup, NC_000023.10:g.2660709_2660712dup, NC_000023.10:g.2660708_2660712dup, NC_000023.10:g.2660707_2660712dup, NC_000023.10:g.2660706_2660712dup, NC_000023.10:g.2660705_2660712dup, NC_000023.10:g.2660704_2660712dup, NC_000023.10:g.2660703_2660712dup, NC_000023.10:g.2660702_2660712dup, NC_000023.10:g.2660701_2660712dup, NC_000023.10:g.2660700_2660712dup, NC_000023.10:g.2660699_2660712dup, NC_000023.10:g.2660697_2660712dup, NC_000023.10:g.2660696_2660712dup, NC_000023.10:g.2660695_2660712dup, NC_000023.10:g.2660694_2660712dup, NC_000023.10:g.2660684_2660712dup, NC_000023.10:g.2660683_2660712dup, NC_000023.10:g.2660712_2660713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.2660712_2660713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.2660712_2660713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.2660712_2660713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.2660712_2660713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.2660712_2660713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.2660712_2660713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.2660712_2660713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.2660712_2660713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.2660712_2660713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.2660712_2660713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.2660712_2660713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

                8.

                rs1491193233 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  ->AG [Show Flanks]
                  Chromosome:
                  Y:2703604 (GRCh38)
                  Y:2571646 (GRCh37)
                  Canonical SPDI:
                  NC_000024.10:2703604:AG:AGAG
                  Gene:
                  CD99 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  AGAG=0./0 (ALFA)
                  AG=0.000035/1 (TOMMO)
                  AG=0.000136/14 (GnomAD)
                  HGVS:

                  9.

                  rs1491184430 has merged into rs4034603 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    AAAAAAAAAAA>-,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA [Show Flanks]
                    Chromosome:
                    Y:2730938 (GRCh38)
                    Y:2598979 (GRCh37)
                    Canonical SPDI:
                    NC_000024.10:2730929:AAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000024.10:2730929:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000024.10:2730929:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000024.10:2730929:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000024.10:2730929:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000024.10:2730929:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000024.10:2730929:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000024.10:2730929:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000024.10:2730929:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000024.10:2730929:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000024.10:2730929:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000024.10:2730929:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000024.10:2730929:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA
                    Gene:
                    CD99 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    AAAAAAAAAAAAA=0./0 (ALFA)
                    HGVS:
                    NC_000024.10:g.2730938_2730948del, NC_000024.10:g.2730943_2730948del, NC_000024.10:g.2730944_2730948del, NC_000024.10:g.2730945_2730948del, NC_000024.10:g.2730946_2730948del, NC_000024.10:g.2730947_2730948del, NC_000024.10:g.2730948del, NC_000024.10:g.2730948dup, NC_000024.10:g.2730947_2730948dup, NC_000024.10:g.2730946_2730948dup, NC_000024.10:g.2730945_2730948dup, NC_000024.10:g.2730944_2730948dup, NC_000024.10:g.2730943_2730948dup, NC_000024.9:g.2598979_2598989del, NC_000024.9:g.2598984_2598989del, NC_000024.9:g.2598985_2598989del, NC_000024.9:g.2598986_2598989del, NC_000024.9:g.2598987_2598989del, NC_000024.9:g.2598988_2598989del, NC_000024.9:g.2598989del, NC_000024.9:g.2598989dup, NC_000024.9:g.2598988_2598989dup, NC_000024.9:g.2598987_2598989dup, NC_000024.9:g.2598986_2598989dup, NC_000024.9:g.2598985_2598989dup, NC_000024.9:g.2598984_2598989dup, NG_009174.1:g.44752_44762del, NG_009174.1:g.44757_44762del, NG_009174.1:g.44758_44762del, NG_009174.1:g.44759_44762del, NG_009174.1:g.44760_44762del, NG_009174.1:g.44761_44762del, NG_009174.1:g.44762del, NG_009174.1:g.44762dup, NG_009174.1:g.44761_44762dup, NG_009174.1:g.44760_44762dup, NG_009174.1:g.44759_44762dup, NG_009174.1:g.44758_44762dup, NG_009174.1:g.44757_44762dup, NC_000023.11:g.2730938_2730948del, NC_000023.11:g.2730943_2730948del, NC_000023.11:g.2730944_2730948del, NC_000023.11:g.2730945_2730948del, NC_000023.11:g.2730946_2730948del, NC_000023.11:g.2730947_2730948del, NC_000023.11:g.2730948del, NC_000023.11:g.2730948dup, NC_000023.11:g.2730947_2730948dup, NC_000023.11:g.2730946_2730948dup, NC_000023.11:g.2730945_2730948dup, NC_000023.11:g.2730944_2730948dup, NC_000023.11:g.2730943_2730948dup, NC_000023.10:g.2648979_2648989del, NC_000023.10:g.2648984_2648989del, NC_000023.10:g.2648985_2648989del, NC_000023.10:g.2648986_2648989del, NC_000023.10:g.2648987_2648989del, NC_000023.10:g.2648988_2648989del, NC_000023.10:g.2648989del, NC_000023.10:g.2648989dup, NC_000023.10:g.2648988_2648989dup, NC_000023.10:g.2648987_2648989dup, NC_000023.10:g.2648986_2648989dup, NC_000023.10:g.2648985_2648989dup, NC_000023.10:g.2648984_2648989dup

                    10.

                    rs1491159192 [Homo sapiens]
                      Variant type:
                      INS
                      Alleles:
                      ->G [Show Flanks]
                      Chromosome:
                      Y:2742020 (GRCh38)
                      Y:2610062 (GRCh37)
                      Canonical SPDI:
                      NC_000024.10:2742020::G
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      G=0./0 (ALFA)
                      G=0.000004/1 (TOPMED)
                      HGVS:

                      11.

                      rs1491150868 has merged into rs906271637 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        TTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT [Show Flanks]
                        Chromosome:
                        Y:2688393 (GRCh38)
                        Y:2556434 (GRCh37)
                        Canonical SPDI:
                        NC_000024.10:2688381:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000024.10:2688381:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000024.10:2688381:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000024.10:2688381:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000024.10:2688381:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000024.10:2688381:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000024.10:2688381:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000024.10:2688381:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000024.10:2688381:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        TTTTTTTTTTTTTT=0./0 (ALFA)
                        HGVS:
                        NC_000024.10:g.2688393_2688398del, NC_000024.10:g.2688395_2688398del, NC_000024.10:g.2688396_2688398del, NC_000024.10:g.2688397_2688398del, NC_000024.10:g.2688398del, NC_000024.10:g.2688398dup, NC_000024.10:g.2688397_2688398dup, NC_000024.10:g.2688396_2688398dup, NC_000024.10:g.2688395_2688398dup, NC_000024.9:g.2556434_2556439del, NC_000024.9:g.2556436_2556439del, NC_000024.9:g.2556437_2556439del, NC_000024.9:g.2556438_2556439del, NC_000024.9:g.2556439del, NC_000024.9:g.2556439dup, NC_000024.9:g.2556438_2556439dup, NC_000024.9:g.2556437_2556439dup, NC_000024.9:g.2556436_2556439dup, NG_009174.1:g.2207_2212del, NG_009174.1:g.2209_2212del, NG_009174.1:g.2210_2212del, NG_009174.1:g.2211_2212del, NG_009174.1:g.2212del, NG_009174.1:g.2212dup, NG_009174.1:g.2211_2212dup, NG_009174.1:g.2210_2212dup, NG_009174.1:g.2209_2212dup, NC_000023.11:g.2688393_2688398del, NC_000023.11:g.2688395_2688398del, NC_000023.11:g.2688396_2688398del, NC_000023.11:g.2688397_2688398del, NC_000023.11:g.2688398del, NC_000023.11:g.2688398dup, NC_000023.11:g.2688397_2688398dup, NC_000023.11:g.2688396_2688398dup, NC_000023.11:g.2688395_2688398dup, NC_000023.10:g.2606434_2606439del, NC_000023.10:g.2606436_2606439del, NC_000023.10:g.2606437_2606439del, NC_000023.10:g.2606438_2606439del, NC_000023.10:g.2606439del, NC_000023.10:g.2606439dup, NC_000023.10:g.2606438_2606439dup, NC_000023.10:g.2606437_2606439dup, NC_000023.10:g.2606436_2606439dup

                        12.

                        rs1491144131 [Homo sapiens]
                          Variant type:
                          DEL
                          Alleles:
                          CT>- [Show Flanks]
                          Chromosome:
                          Y:2742640 (GRCh38)
                          Y:2610681 (GRCh37)
                          Canonical SPDI:
                          NC_000024.10:2742639:CT:
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          -=0.00008/1 (ALFA)
                          -=0.00086/70 (GnomAD)
                          HGVS:

                          13.

                          rs1491121829 [Homo sapiens]
                            Variant type:
                            DEL
                            Alleles:
                            CC>- [Show Flanks]
                            Chromosome:
                            Y:2732877 (GRCh38)
                            Y:2600918 (GRCh37)
                            Canonical SPDI:
                            NC_000024.10:2732876:CC:
                            Gene:
                            CD99 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            -=0./0 (ALFA)
                            -=0.000007/1 (GnomAD)
                            HGVS:

                            14.

                            rs1491108050 [Homo sapiens]
                              Variant type:
                              DEL
                              Alleles:
                              AA>- [Show Flanks]
                              Chromosome:
                              Y:2703604 (GRCh38)
                              Y:2571645 (GRCh37)
                              Canonical SPDI:
                              NC_000024.10:2703603:AA:
                              Gene:
                              CD99 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              -=0.001621/19 (ALFA)
                              -=0.000035/1 (TOMMO)
                              -=0.016847/2123 (GnomAD)
                              HGVS:

                              15.

                              rs1491094933 [Homo sapiens]
                                Variant type:
                                DEL
                                Alleles:
                                TG>- [Show Flanks]
                                Chromosome:
                                Y:2688398 (GRCh38)
                                Y:2556439 (GRCh37)
                                Canonical SPDI:
                                NC_000024.10:2688397:TG:
                                HGVS:

                                16.

                                rs1491062619 has merged into rs200451375 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  TT>-,T,TTTT [Show Flanks]
                                  Chromosome:
                                  Y:2732576 (GRCh38)
                                  Y:2600617 (GRCh37)
                                  Canonical SPDI:
                                  NC_000024.10:2732573:TTTT:TT,NC_000024.10:2732573:TTTT:TTT,NC_000024.10:2732573:TTTT:TTTTTT
                                  Gene:
                                  CD99 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  TTTT=0.000071/1 (ALFA)
                                  -=0.000044/1 (TOMMO)
                                  -=0.000052/7 (GnomAD)
                                  -=0.000076/20 (TOPMED)
                                  HGVS:

                                  17.

                                  rs1490938090 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>T [Show Flanks]
                                    Chromosome:
                                    Y:2733279 (GRCh38)
                                    Y:2601320 (GRCh37)
                                    Canonical SPDI:
                                    NC_000024.10:2733278:G:T
                                    Gene:
                                    CD99 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    T=0./0 (ALFA)
                                    T=0.000004/1 (TOPMED)
                                    HGVS:

                                    18.

                                    rs1490919425 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      G>A [Show Flanks]
                                      Chromosome:
                                      Y:2688205 (GRCh38)
                                      Y:2556246 (GRCh37)
                                      Canonical SPDI:
                                      NC_000024.10:2688204:G:A
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      A=0./0 (ALFA)
                                      HGVS:

                                      19.

                                      rs1490862611 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>C [Show Flanks]
                                        Chromosome:
                                        Y:2689048 (GRCh38)
                                        Y:2557089 (GRCh37)
                                        Canonical SPDI:
                                        NC_000024.10:2689047:T:C
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        C=0.000071/1 (ALFA)
                                        C=0.000008/2 (TOPMED)
                                        C=0.000014/2 (GnomAD)
                                        C=0.000035/1 (TOMMO)
                                        HGVS:

                                        20.

                                        rs1490850433 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>C [Show Flanks]
                                          Chromosome:
                                          Y:2701354 (GRCh38)
                                          Y:2569395 (GRCh37)
                                          Canonical SPDI:
                                          NC_000024.10:2701353:G:C
                                          Gene:
                                          CD99 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          C=0./0 (ALFA)
                                          C=0.000004/1 (TOPMED)
                                          HGVS:

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