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Items: 1 to 20 of 243

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128786insertion1nstd186human GRCh37 chr3: 124,753,039-124,753,087 , GRCh38.p12 chr3: 125,034,195-125,034,243 HEG1
    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
    nsv5948375insertion1nstd209human GRCh38 chr3: 125,034,192-125,034,192 , GRCh37.p13 chr3: 124,753,036-124,753,036 HEG1
    nsv5893678copy number variation1nstd209human GRCh38 chr3: 125,028,024-125,028,099 , GRCh37.p13 chr3: 124,746,868-124,746,943 HEG1
    nsv5617758insertion1nstd207human GRCh38 chr3: 124,987,952-124,987,952 , GRCh37.p13 chr3: 124,706,796-124,706,796 HEG1
    nsv5605162insertion1nstd207human GRCh38 chr3: 125,034,192-125,034,192 , GRCh37.p13 chr3: 124,753,036-124,753,036 HEG1
    nsv5563808inversion1nstd206human GRCh38 chr3: 125,018,836-125,019,767 , GRCh37.p13 chr3: 124,737,680-124,738,611 HEG1
    nsv5561131sequence alteration1nstd206human GRCh38 chr3: 125,018,861-125,019,724 , GRCh37.p13 chr3: 124,737,705-124,738,568 HEG1
    nsv5537173insertion1nstd206human GRCh38 chr3: 125,034,195-125,034,243 , GRCh37.p13 chr3: 124,753,039-124,753,087 HEG1
    nsv5453393copy number variation1nstd206human GRCh38 chr3: 125,028,027-125,028,094 , GRCh37.p13 chr3: 124,746,871-124,746,938 HEG1
    nsv5346490translocation1nstd200human GRCh38 chr3: 125,028,094-125,028,094 , GRCh38 chr3: 125,028,027-125,028,027 , GRCh37.p13 chr3: 124,746,871-124,746,871 , GRCh37.p13 chr3: 124,746,938-124,746,938 HEG1
    nsv5306632copy number variation1nstd204human GRCh38.p13 chr3: 125,028,022-125,028,098 , GRCh37.p13 chr3: 124,746,866-124,746,942 HEG1
    nsv5238107copy number variation1nstd204human GRCh38.p13 chr3: 124,981,832-124,982,978 , GRCh37.p13 chr3: 124,700,676-124,701,822 HEG1
    nsv5227855copy number variation1nstd204human GRCh38.p13 chr3: 124,981,732-124,984,208 , GRCh37.p13 chr3: 124,700,576-124,703,052 HEG1
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4919921copy number variation1nstd200human GRCh38 chr3: 124,999,989-125,000,251 , GRCh37.p13 chr3: 124,718,833-124,719,095 HEG1
    nsv4919920copy number variation1nstd200human GRCh38 chr3: 124,985,874-124,987,613 , GRCh37.p13 chr3: 124,704,718-124,706,457 HEG1
    nsv4762979insertion1nstd199human GRCh37 chr3: 124,706,794-124,706,794 , GRCh38.p12 chr3: 124,987,950-124,987,950 HEG1
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