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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 RNU6-789P, FAM86HP, 169 more genes
    nsv6112709copy number variation1nstd102humanPathogenic GRCh37 chr3: 123,000,000-129,700,000 , GRCh38.p12 chr3: 123,281,153-129,981,157 OR7E97P, MARK3P3, 160 more genes
    nsv5954561insertion1nstd209human GRCh38 chr3: 129,465,635-129,465,635 , GRCh37.p13 chr3: 129,184,478-129,184,478 IFT122
    nsv5906118copy number variation1nstd209human GRCh38 chr3: 129,426,491-129,446,350 , GRCh37.p13 chr3: 129,145,334-129,165,193 IFT122, MBD4, 1 more genes
    nsv5897732copy number variation1nstd209human GRCh38 chr3: 129,465,624-129,465,933 , GRCh37.p13 chr3: 129,184,467-129,184,776 IFT122
    nsv5892095copy number variation1nstd209human GRCh38 chr3: 129,516,132-129,516,229 , GRCh37.p13 chr3: 129,234,975-129,235,072 IFT122
    nsv5833985copy number variation1nstd209human GRCh38 chr3: 129,426,412-129,445,475 , GRCh37.p13 chr3: 129,145,255-129,164,318 MBD4, EFCAB12, 1 more genes
    nsv5718022mobile element insertion1nstd211human GRCh38 chr3: 129,475,003-129,475,003 , GRCh37.p13 chr3: 129,193,846-129,193,846 IFT122
    nsv5574279copy number variation1nstd207human GRCh38 chr3: 129,465,624-129,465,933 , GRCh37.p13 chr3: 129,184,467-129,184,776 IFT122
    nsv5451171copy number variation1nstd206human GRCh38 chr3: 129,380,519-129,487,453 , GRCh37.p13 chr3: 129,099,362-129,206,296 IFT122, EFCAB12, 3 more genes
    nsv5442058copy number variation1nstd206human GRCh38 chr3: 129,465,643-129,465,934 , GRCh37.p13 chr3: 129,184,486-129,184,777 IFT122
    nsv5381960mobile element deletion2nstd186human GRCh37 chr3: 129,184,486-129,184,777 , GRCh38.p12 chr3: 129,465,643-129,465,934 IFT122
    nsv5381590copy number variation1nstd102humanUncertain significance GRCh37 chr3: 129,234,311-129,252,561 , GRCh38.p12 chr3: 129,515,468-129,533,718 RHO, IFT122
    nsv5204982mobile element deletion1nstd204human GRCh38.p13 chr3: 129,465,643-129,465,934 , GRCh37.p13 chr3: 129,184,486-129,184,777 IFT122
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4920074copy number variation1nstd200human GRCh38 chr3: 129,515,411-129,517,020 , GRCh37.p13 chr3: 129,234,254-129,235,863 IFT122
    nsv4914756copy number variation1nstd200human GRCh38 chr3: 129,384,416-129,491,454 , GRCh37.p13 chr3: 129,103,259-129,210,297 IFT122, EFCAB12, 3 more genes
    nsv4870029mobile element deletion1nstd200human GRCh38 chr3: 129,465,643-129,465,934 , GRCh37.p13 chr3: 129,184,486-129,184,777 IFT122
    nsv4791017copy number variation1nstd200human GRCh37 chr3: 129,234,879-129,235,688 , GRCh38.p12 chr3: 129,516,036-129,516,845 IFT122
    nsv4791016copy number variation1nstd200human GRCh37 chr3: 129,234,254-129,235,863 , GRCh38.p12 chr3: 129,515,411-129,517,020 IFT122
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