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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7094213copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-4,796,274 , GRCh38.p12 chr12: 4,259,186-4,687,108 RPS15P7, RAD51AP1, 11 more genes
    nsv7094047copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-9,027,607 , GRCh38.p12 chr12: 4,259,186-8,875,011 ACRBP, OR7E148P, 165 more genes
    nsv7094046copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-5,155,155 , GRCh38.p12 chr12: 4,259,186-5,045,989 RPS15P7, CCND2, 18 more genes
    nsv7077218inversion1nstd229human GRCh38 chr12: 4,327,468-4,340,520 , GRCh37.p13 chr12: 4,436,634-4,449,686 TIGAR
    nsv7072221inversion1nstd229human GRCh38 chr12: 4,055,290-11,695,188 , GRCh37.p13 chr12: 4,164,456-11,848,122 RN7SL69P, KLRA1P, 285 more genes
    nsv7068624inversion1nstd229human GRCh38 chr12: 2,500,360-5,372,895 , GRCh37.p13 chr12: 2,609,526-5,482,061 LOC105369607, IQSEC3P1, 62 more genes
    nsv7067673inversion1nstd229human GRCh38 chr12: 4,264,356-4,363,276 , GRCh37.p13 chr12: 4,373,522-4,472,442 RPS15P7, CCND2-AS1, 2 more genes
    nsv7062176inversion1nstd229human GRCh38 chr12: 4,309,330-4,334,351 , GRCh37.p13 chr12: 4,418,496-4,443,517 TIGAR, RPS15P7
    nsv6935680copy number variation1nstd229human GRCh38 chr12: 4,357,842-4,358,159 , GRCh37.p13 chr12: 4,467,008-4,467,325 TIGAR
    nsv6934949copy number variation1nstd229human GRCh38 chr12: 4,322,801-4,325,400 , GRCh37.p13 chr12: 4,431,967-4,434,566 TIGAR, RPS15P7
    nsv6934495copy number variation1nstd229human GRCh38 chr12: 4,358,239-4,365,694 , GRCh37.p13 chr12: 4,467,405-4,474,860 TIGAR
    nsv6931013copy number variation1nstd229human GRCh38 chr12: 4,335,593-4,573,659 , GRCh37.p13 chr12: 4,444,759-4,682,825 TIGAR, FGF6, 4 more genes
    nsv6920853copy number variation1nstd229human GRCh38 chr12: 4,319,789-4,319,873 , GRCh37.p13 chr12: 4,428,955-4,429,039 TIGAR
    nsv6919549copy number variation1nstd229human GRCh38 chr12: 4,340,166-4,348,779 , GRCh37.p13 chr12: 4,449,332-4,457,945 TIGAR
    nsv6913746copy number variation1nstd229human GRCh38 chr12: 3,972,756-5,647,610 , GRCh37.p13 chr12: 4,081,922-5,756,776 LOC101901829, LOC100420673, 29 more genes
    nsv6637376copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,787-8,320,544 , GRCh38.p12 chr12: 64,621-8,167,948 GCSHP4, RNU7-1, 220 more genes
    nsv6594791inversion1nstd223human GRCh38 chr12: 4,337,311-4,338,098 , GRCh37.p13 chr12: 4,446,477-4,447,264 TIGAR
    nsv6594677inversion1nstd223human GRCh38 chr12: 4,324,943-4,325,576 , GRCh37.p13 chr12: 4,434,109-4,434,742 RPS15P7, TIGAR
    nsv6473617copy number variation1nstd223human GRCh38 chr12: 3,972,756-5,647,610 , GRCh37.p13 chr12: 4,081,922-5,756,776 KCNA5, LINC02443, 29 more genes
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