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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6112688copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144 RNU4-62P, MTCO1P29, 169 more genes
    nsv5899617copy number variation1nstd209human GRCh38 chr3: 126,524,098-126,529,359 , GRCh37.p13 chr3: 126,242,941-126,248,202 C3orf22, CHST13
    nsv5898503copy number variation1nstd209human GRCh38 chr3: 126,539,488-126,539,631 , GRCh37.p13 chr3: 126,258,331-126,258,474 CHST13, C3orf22
    nsv5891726copy number variation1nstd209human GRCh38 chr3: 126,535,061-126,535,556 , GRCh37.p13 chr3: 126,253,904-126,254,399 CHST13, C3orf22
    nsv5890794copy number variation1nstd209human GRCh38 chr3: 126,556,879-126,556,930 , GRCh37.p13 chr3: 126,275,722-126,275,773 C3orf22
    nsv5834637copy number variation2nstd209human GRCh38 chr3: 126,525,717-126,526,848 , GRCh37.p13 chr3: 126,244,560-126,245,691 C3orf22, CHST13
    nsv5834580copy number variation1nstd209human GRCh38 chr3: 126,524,075-126,529,927 , GRCh37.p13 chr3: 126,242,918-126,248,770 C3orf22, CHST13
    nsv5608325insertion1nstd207human GRCh38 chr3: 126,539,875-126,539,875 , GRCh37.p13 chr3: 126,258,718-126,258,718 C3orf22, CHST13
    nsv5544096insertion1nstd206human GRCh38 chr3: 126,539,880-126,539,926 , GRCh37.p13 chr3: 126,258,723-126,258,769 CHST13, C3orf22
    nsv5541637insertion1nstd206human GRCh38 chr3: 126,559,162-126,559,162 , GRCh37.p13 chr3: 126,278,005-126,278,005 C3orf22, LOC105374090
    nsv5444652copy number variation1nstd206human GRCh38 chr3: 126,535,093-126,535,529 , GRCh37.p13 chr3: 126,253,936-126,254,372 C3orf22, CHST13
    nsv5354685translocation1nstd200human GRCh38 chr1: 16,352,221-16,352,221 , GRCh38 chr3: 126,559,162-126,559,162 , GRCh37.p13 chr1: 16,678,716-16,678,716 , GRCh37.p13 chr3: 126,278,005-126,278,005 FBXO42, C3orf22, 1 more genes
    nsv5343032translocation1nstd200human GRCh37 chr1: 16,678,716-16,678,716 , GRCh37 chr3: 126,278,005-126,278,005 , GRCh38.p12 chr1: 16,352,221-16,352,221 , GRCh38.p12 chr3: 126,559,162-126,559,162 FBXO42, C3orf22, 1 more genes
    nsv5329331translocation1nstd204human GRCh37.p13 chr3: 126,278,005-126,278,005 , GRCh38.p13 chr3: 126,559,162-126,559,162 , GRCh38.p13 chr1: 16,352,221-16,352,221 , GRCh37.p13 chr1: 16,678,716-16,678,716 FBXO42, C3orf22, 1 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4919961copy number variation1nstd200human GRCh38 chr3: 126,557,885-126,563,880 , GRCh37.p13 chr3: 126,276,728-126,282,723 C3orf22, RNA5SP138, 1 more genes
    nsv4919960copy number variation1nstd200human GRCh38 chr3: 126,525,753-126,526,575 , GRCh37.p13 chr3: 126,244,596-126,245,418 C3orf22, CHST13
    nsv4914726copy number variation1nstd200human GRCh38 chr3: 126,551,479-126,551,812 , GRCh37.p13 chr3: 126,270,322-126,270,655 C3orf22
    nsv4807069copy number variation1nstd200human GRCh37 chr3: 126,276,728-126,282,723 , GRCh38.p12 chr3: 126,557,885-126,563,880 RNA5SP138, C3orf22, 1 more genes
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