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Items: 1 to 20 of 16834

1.

rs1491526885 has merged into rs3045400 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    TGTGTGTGTGTGTGTGTG>-,TG,TGTG,TGTGTG,TGTGTGTG,TGTGTGTGTG,TGTGTGTGTGTG,TGTGTGTGTGTGTG,TGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG [Show Flanks]
    Chromosome:
    1:147587779 (GRCh38)
    1:147059584 (GRCh37)
    Canonical SPDI:
    NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:147587756:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
    Gene:
    BCL9 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    TGTGTGTGTGTGTGTGTGTGTGTG=0./0 (ALFA)
    TGTGTGTGTGTGTGTG=0.000004/1 (TOPMED)
    -=0.466653/2337 (1000Genomes)
    HGVS:
    NC_000001.11:g.147587757TG[11], NC_000001.11:g.147587757TG[12], NC_000001.11:g.147587757TG[13], NC_000001.11:g.147587757TG[14], NC_000001.11:g.147587757TG[15], NC_000001.11:g.147587757TG[16], NC_000001.11:g.147587757TG[17], NC_000001.11:g.147587757TG[18], NC_000001.11:g.147587757TG[19], NC_000001.11:g.147587757TG[21], NC_000001.11:g.147587757TG[22], NC_000001.11:g.147587757TG[23], NC_000001.11:g.147587757TG[24], NC_000001.11:g.147587757TG[25], NC_000001.11:g.147587757TG[26], NC_000001.11:g.147587757TG[27], NC_000001.11:g.147587757TG[28], NC_000001.11:g.147587757TG[34], NW_003871055.3:g.4403170TG[11], NW_003871055.3:g.4403170TG[12], NW_003871055.3:g.4403170TG[13], NW_003871055.3:g.4403170TG[14], NW_003871055.3:g.4403170TG[15], NW_003871055.3:g.4403170TG[16], NW_003871055.3:g.4403170TG[17], NW_003871055.3:g.4403170TG[18], NW_003871055.3:g.4403170TG[19], NW_003871055.3:g.4403170TG[21], NW_003871055.3:g.4403170TG[22], NW_003871055.3:g.4403170TG[23], NW_003871055.3:g.4403170TG[24], NW_003871055.3:g.4403170TG[25], NW_003871055.3:g.4403170TG[26], NW_003871055.3:g.4403170TG[27], NW_003871055.3:g.4403170TG[28], NW_003871055.3:g.4403170TG[34], NC_000001.10:g.147059562TG[20], NC_000001.10:g.147059562TG[11], NC_000001.10:g.147059562TG[12], NC_000001.10:g.147059562TG[13], NC_000001.10:g.147059562TG[14], NC_000001.10:g.147059562TG[15], NC_000001.10:g.147059562TG[16], NC_000001.10:g.147059562TG[18], NC_000001.10:g.147059562TG[19], NC_000001.10:g.147059562TG[21], NC_000001.10:g.147059562TG[22], NC_000001.10:g.147059562TG[23], NC_000001.10:g.147059562TG[24], NC_000001.10:g.147059562TG[25], NC_000001.10:g.147059562TG[26], NC_000001.10:g.147059562TG[27], NC_000001.10:g.147059562TG[28], NC_000001.10:g.147059562TG[34]

    2.

    rs1491475694 has merged into rs72473603 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      TTTTTTTTTTT>-,T,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTCTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
      Chromosome:
      1:147548986 (GRCh38)
      1:147020757 (GRCh37)
      Canonical SPDI:
      NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTCTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
      Gene:
      BCL9 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      TTTTTT=0./0 (ALFA)
      -=0.000004/1 (TOPMED)
      HGVS:
      NC_000001.11:g.147548986_147548996del, NC_000001.11:g.147548987_147548996del, NC_000001.11:g.147548989_147548996del, NC_000001.11:g.147548990_147548996del, NC_000001.11:g.147548991_147548996del, NC_000001.11:g.147548993_147548996del, NC_000001.11:g.147548994_147548996del, NC_000001.11:g.147548995_147548996del, NC_000001.11:g.147548996del, NC_000001.11:g.147548996dup, NC_000001.11:g.147548995_147548996dup, NC_000001.11:g.147548994_147548996dup, NC_000001.11:g.147548993_147548996dup, NC_000001.11:g.147548992_147548996dup, NC_000001.11:g.147548991_147548996dup, NC_000001.11:g.147548990_147548996dup, NC_000001.11:g.147548989_147548996dup, NC_000001.11:g.147548988_147548996dup, NC_000001.11:g.147548987_147548996dup, NC_000001.11:g.147548986_147548996dup, NC_000001.11:g.147548985_147548996dup, NC_000001.11:g.147548984_147548996dup, NC_000001.11:g.147548983_147548996dup, NC_000001.11:g.147548982_147548996dup, NC_000001.11:g.147548980_147548996T[32]GTTTTTTTTTTTTTTTTTT[1], NC_000001.11:g.147548981_147548996dup, NC_000001.11:g.147548980_147548996dup, NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTT, NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.147548980_147548996T[39]CTTT[3]T[17], NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.4364399_4364409del, NW_003871055.3:g.4364400_4364409del, NW_003871055.3:g.4364402_4364409del, NW_003871055.3:g.4364403_4364409del, NW_003871055.3:g.4364404_4364409del, NW_003871055.3:g.4364406_4364409del, NW_003871055.3:g.4364407_4364409del, NW_003871055.3:g.4364408_4364409del, NW_003871055.3:g.4364409del, NW_003871055.3:g.4364409dup, NW_003871055.3:g.4364408_4364409dup, NW_003871055.3:g.4364407_4364409dup, NW_003871055.3:g.4364406_4364409dup, NW_003871055.3:g.4364405_4364409dup, NW_003871055.3:g.4364404_4364409dup, NW_003871055.3:g.4364403_4364409dup, NW_003871055.3:g.4364402_4364409dup, NW_003871055.3:g.4364401_4364409dup, NW_003871055.3:g.4364400_4364409dup, NW_003871055.3:g.4364399_4364409dup, NW_003871055.3:g.4364398_4364409dup, NW_003871055.3:g.4364397_4364409dup, NW_003871055.3:g.4364396_4364409dup, NW_003871055.3:g.4364395_4364409dup, NW_003871055.3:g.4364393_4364409T[32]GTTTTTTTTTTTTTTTTTT[1], NW_003871055.3:g.4364394_4364409dup, NW_003871055.3:g.4364393_4364409dup, NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.4364393_4364409T[39]CTTT[3]T[17], NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.147020759_147020769del, NC_000001.10:g.147020760_147020769del, NC_000001.10:g.147020762_147020769del, NC_000001.10:g.147020763_147020769del, NC_000001.10:g.147020764_147020769del, NC_000001.10:g.147020766_147020769del, NC_000001.10:g.147020767_147020769del, NC_000001.10:g.147020768_147020769del, NC_000001.10:g.147020769del, NC_000001.10:g.147020769dup, NC_000001.10:g.147020768_147020769dup, NC_000001.10:g.147020767_147020769dup, NC_000001.10:g.147020766_147020769dup, NC_000001.10:g.147020765_147020769dup, NC_000001.10:g.147020764_147020769dup, NC_000001.10:g.147020763_147020769dup, NC_000001.10:g.147020762_147020769dup, NC_000001.10:g.147020761_147020769dup, NC_000001.10:g.147020760_147020769dup, NC_000001.10:g.147020759_147020769dup, NC_000001.10:g.147020758_147020769dup, NC_000001.10:g.147020757_147020769dup, NC_000001.10:g.147020756_147020769dup, NC_000001.10:g.147020755_147020769dup, NC_000001.10:g.147020752_147020769T[33]GTTTTTTTTTTTTTTTTTT[1], NC_000001.10:g.147020754_147020769dup, NC_000001.10:g.147020753_147020769dup, NC_000001.10:g.147020752_147020769dup, NC_000001.10:g.147020751_147020769dup, NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.147020751_147020769T[41]CTTT[3]T[17], NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

      3.

      rs1491455940 has merged into rs202085114 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        T>-,TT,TTT,TTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTTTTTT [Show Flanks]
        Chromosome:
        1:147622969 (GRCh38)
        1:147094770 (GRCh37)
        Canonical SPDI:
        NC_000001.11:147622968:TTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:147622968:TTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:147622968:TTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:147622968:TTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:147622968:TTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:147622968:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:147622968:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:147622968:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
        Gene:
        BCL9 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        TTTTTTTTTTTTTT=0./0 (ALFA)
        T=0.0002/1 (1000Genomes)
        HGVS:
        NC_000001.11:g.147622979del, NC_000001.11:g.147622979dup, NC_000001.11:g.147622978_147622979dup, NC_000001.11:g.147622977_147622979dup, NC_000001.11:g.147622974_147622979dup, NC_000001.11:g.147622973_147622979dup, NC_000001.11:g.147622972_147622979dup, NC_000001.11:g.147622979_147622980insTTTTTTTTTTTTTT, NW_003871055.3:g.4438392del, NW_003871055.3:g.4438392dup, NW_003871055.3:g.4438391_4438392dup, NW_003871055.3:g.4438390_4438392dup, NW_003871055.3:g.4438387_4438392dup, NW_003871055.3:g.4438386_4438392dup, NW_003871055.3:g.4438385_4438392dup, NW_003871055.3:g.4438392_4438393insTTTTTTTTTTTTTT, NC_000001.10:g.147094781del, NC_000001.10:g.147094781dup, NC_000001.10:g.147094780_147094781dup, NC_000001.10:g.147094779_147094781dup, NC_000001.10:g.147094776_147094781dup, NC_000001.10:g.147094775_147094781dup, NC_000001.10:g.147094774_147094781dup, NC_000001.10:g.147094781_147094782insTTTTTTTTTTTTTT

        4.

        rs1491390215 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          CT>- [Show Flanks]
          Chromosome:
          1:147596411 (GRCh38)
          1:147068202 (GRCh37)
          Canonical SPDI:
          NC_000001.11:147596409:TCT:T
          Gene:
          BCL9 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          T=0.00008/1 (ALFA)
          -=0.00308/2 (GnomAD)
          HGVS:

          5.

          rs1491335167 [Homo sapiens]
            Variant type:
            INS
            Alleles:
            ->G [Show Flanks]
            Chromosome:
            1:147599489 (GRCh38)
            1:147071283 (GRCh37)
            Canonical SPDI:
            NC_000001.11:147599489::G
            Gene:
            BCL9 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            G=0./0 (ALFA)
            G=0.000004/1 (TOPMED)
            G=0.000048/6 (GnomAD)
            HGVS:

            6.

            rs1491306981 has merged into rs1553200491 [Homo sapiens]
              Variant type:
              INS
              Alleles:
              ->TTC,TTCTTTC [Show Flanks]
              Chromosome:
              1:147596410 (GRCh38)
              1:147068202 (GRCh37)
              Canonical SPDI:
              NC_000001.11:147596410::TTC,NC_000001.11:147596410::TTCTTTC
              Gene:
              BCL9 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              TTCTTTC=0./0 (ALFA)
              TTC=0.00078/5 (1000Genomes)
              TTC=0.00125/1 (GnomAD)
              HGVS:

              7.

              rs1491271185 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                ->CTTT,GTTT [Show Flanks]
                Chromosome:
                1:147548980 (GRCh38)
                1:147020754 (GRCh37)
                Canonical SPDI:
                NC_000001.11:147548980:TTT:TTTCTTT,NC_000001.11:147548980:TTT:TTTGTTT
                Gene:
                BCL9 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                TTTGTTT=0./0 (ALFA)
                HGVS:

                8.

                rs1491264242 has merged into rs11292399 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  TTTTTT>-,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT [Show Flanks]
                  Chromosome:
                  1:147559135 (GRCh38)
                  1:147030911 (GRCh37)
                  Canonical SPDI:
                  NC_000001.11:147559128:TTTTTTTTTTTT:TTTTTT,NC_000001.11:147559128:TTTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:147559128:TTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:147559128:TTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:147559128:TTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:147559128:TTTTTTTTTTTT:TTTTTTTTTTTTTTT
                  Gene:
                  BCL9 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  TTTTTTTTTTT=0./0 (ALFA)
                  HGVS:

                  9.

                  rs1491149528 [Homo sapiens]
                    Variant type:
                    DEL
                    Alleles:
                    CT>- [Show Flanks]
                    Chromosome:
                    1:147622968 (GRCh38)
                    1:-1 (GRCh37)
                    Canonical SPDI:
                    NC_000001.11:147622967:CT:
                    Gene:
                    BCL9 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    -=0.00007/1 (ALFA)
                    -=0.00018/1 (GnomAD)
                    HGVS:

                    10.

                    rs1491057681 has merged into rs34799247 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      GC>-,GCGC [Show Flanks]
                      Chromosome:
                      1:147599494 (GRCh38)
                      1:147071288 (GRCh37)
                      Canonical SPDI:
                      NC_000001.11:147599492:CGC:C,NC_000001.11:147599492:CGC:CGCGC
                      Gene:
                      BCL9 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      C=0.016512/232 (ALFA)
                      CG=0.000073/1 (TOMMO)
                      -=0.012543/3320 (TOPMED)
                      -=0.014679/1839 (GnomAD)
                      HGVS:

                      11.

                      rs1491043330 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        GA>- [Show Flanks]
                        Chromosome:
                        1:147569489 (GRCh38)
                        1:147041273 (GRCh37)
                        Canonical SPDI:
                        NC_000001.11:147569487:AGA:A
                        Gene:
                        BCL9 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        A=0.00017/2 (ALFA)
                        -=0.00186/50 (TOMMO)
                        -=0.02653/13 (GnomAD)
                        HGVS:

                        12.

                        rs1491001266 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          T>C [Show Flanks]
                          Chromosome:
                          1:147565248 (GRCh38)
                          1:147037027 (GRCh37)
                          Canonical SPDI:
                          NC_000001.11:147565247:T:C
                          Gene:
                          BCL9 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          C=0./0 (ALFA)
                          C=0.000007/1 (GnomAD)
                          C=0.000008/2 (TOPMED)
                          HGVS:

                          13.

                          rs1490957282 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            T>C [Show Flanks]
                            Chromosome:
                            1:147622887 (GRCh38)
                            1:147094688 (GRCh37)
                            Canonical SPDI:
                            NC_000001.11:147622886:T:C
                            Gene:
                            BCL9 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            C=0./0 (ALFA)
                            C=0.000004/1 (TOPMED)
                            HGVS:

                            14.

                            rs1490950222 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              C>T [Show Flanks]
                              Chromosome:
                              1:147566292 (GRCh38)
                              1:147038071 (GRCh37)
                              Canonical SPDI:
                              NC_000001.11:147566291:C:T
                              Gene:
                              BCL9 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              T=0./0 (ALFA)
                              T=0.000014/2 (GnomAD)
                              T=0.000015/4 (TOPMED)
                              HGVS:

                              15.

                              rs1490921549 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>A [Show Flanks]
                                Chromosome:
                                1:147581157 (GRCh38)
                                1:147052957 (GRCh37)
                                Canonical SPDI:
                                NC_000001.11:147581156:C:A
                                Gene:
                                BCL9 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                A=0.000071/1 (ALFA)
                                A=0.000021/3 (GnomAD)
                                A=0.000034/9 (TOPMED)
                                HGVS:

                                16.

                                rs1490855783 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  C>G [Show Flanks]
                                  Chromosome:
                                  1:147582322 (GRCh38)
                                  1:147054122 (GRCh37)
                                  Canonical SPDI:
                                  NC_000001.11:147582321:C:G
                                  Gene:
                                  BCL9 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  G=0./0 (ALFA)
                                  G=0.000004/1 (TOPMED)
                                  G=0.000007/1 (GnomAD)
                                  HGVS:

                                  17.

                                  rs1490820729 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    T>A [Show Flanks]
                                    Chromosome:
                                    1:147573527 (GRCh38)
                                    1:147045318 (GRCh37)
                                    Canonical SPDI:
                                    NC_000001.11:147573526:T:A
                                    Gene:
                                    BCL9 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    A=0./0 (ALFA)
                                    A=0.000007/1 (GnomAD)
                                    A=0.000011/3 (TOPMED)
                                    HGVS:

                                    18.

                                    rs1490741678 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      T>A,C [Show Flanks]
                                      Chromosome:
                                      1:147590719 (GRCh38)
                                      1:147062508 (GRCh37)
                                      Canonical SPDI:
                                      NC_000001.11:147590718:T:A,NC_000001.11:147590718:T:C
                                      Gene:
                                      BCL9 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      A=0.000071/1 (ALFA)
                                      A=0.000007/1 (GnomAD)
                                      A=0.000011/3 (TOPMED)
                                      HGVS:

                                      19.

                                      rs1490719006 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>C [Show Flanks]
                                        Chromosome:
                                        1:147604774 (GRCh38)
                                        1:147076567 (GRCh37)
                                        Canonical SPDI:
                                        NC_000001.11:147604773:T:C
                                        Gene:
                                        BCL9 (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        C=0.000071/1 (ALFA)
                                        C=0.000004/1 (TOPMED)
                                        HGVS:

                                        20.

                                        rs1490657211 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          A>C,T [Show Flanks]
                                          Chromosome:
                                          1:147539603 (GRCh38)
                                          1:147011424 (GRCh37)
                                          Canonical SPDI:
                                          NC_000001.11:147539602:A:C,NC_000001.11:147539602:A:T
                                          Gene:
                                          BCL9 (Varview)
                                          Functional Consequence:
                                          upstream_transcript_variant,2KB_upstream_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          T=0./0 (ALFA)
                                          T=0.000019/5 (TOPMED)
                                          T=0.000021/3 (GnomAD)
                                          HGVS:

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