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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5685922mobile element insertion1nstd211human GRCh38 chr3: 119,221,837-119,221,837 , GRCh37.p13 chr3: 118,940,684-118,940,684 B4GALT4
    nsv5605501insertion1nstd207human GRCh38 chr3: 119,210,532-119,210,532 , GRCh37.p13 chr3: 118,929,379-118,929,379 B4GALT4
    nsv5447678copy number variation1nstd206human GRCh38 chr3: 119,136,526-119,283,873 , GRCh37.p13 chr3: 118,855,373-119,002,720 IGSF11, UPK1B, 3 more genes
    nsv5438780copy number variation1nstd206human GRCh38 chr3: 119,228,790-119,228,848 , GRCh37.p13 chr3: 118,947,637-118,947,695 B4GALT4-AS1, B4GALT4
    nsv5361874translocation1nstd200human GRCh38 chr3: 119,211,634-119,211,634 , GRCh38 chr3: 119,210,235-119,210,235 , GRCh37.p13 chr3: 118,929,082-118,929,082 , GRCh37.p13 chr3: 118,930,481-118,930,481 B4GALT4
    nsv5361873translocation1nstd200human GRCh38 chr3: 119,210,230-119,210,230 , GRCh38 chr3: 119,211,821-119,211,821 , GRCh37.p13 chr3: 118,930,668-118,930,668 , GRCh37.p13 chr3: 118,929,077-118,929,077 B4GALT4
    nsv5175018mobile element insertion1nstd203human GRCh38 chr3: 119,231,833-119,231,850 , GRCh37.p13 chr3: 118,950,680-118,950,697 B4GALT4-AS1, B4GALT4
    nsv5093453mobile element insertion1nstd203human GRCh38 chr3: 119,226,566-119,226,580 , GRCh37.p13 chr3: 118,945,413-118,945,427 B4GALT4-AS1, B4GALT4
    nsv5091050mobile element insertion1nstd203human GRCh38 chr3: 119,226,564-119,226,580 , GRCh37.p13 chr3: 118,945,411-118,945,427 B4GALT4, B4GALT4-AS1
    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
    nsv4919755copy number variation1nstd200human GRCh38 chr3: 118,773,498-119,384,319 , GRCh37.p13 chr3: 118,492,345-119,103,166 TEX55, LOC105374060, 10 more genes
    nsv4914686copy number variation1nstd200human GRCh38 chr3: 119,207,027-119,209,986 , GRCh37.p13 chr3: 118,925,874-118,928,833 B4GALT4
    nsv4806918copy number variation1nstd200human GRCh37 chr3: 118,855,373-119,002,720 , GRCh38.p12 chr3: 119,136,526-119,283,873 TEX55, B4GALT4, 3 more genes
    nsv4794315copy number variation1nstd200human GRCh37 chr3: 118,953,915-118,958,778 , GRCh38.p12 chr3: 119,235,068-119,239,931 B4GALT4-AS1, B4GALT4
    nsv4728686copy number variation1nstd102humanUncertain significance GRCh37 chr3: 118,733,449-118,963,249 , GRCh38.p12 chr3: 119,014,602-119,244,402 IGSF11, TEX55, 3 more genes
    nsv4637675copy number variation1nstd186human GRCh37 chr3: 118,947,435-118,947,695 , GRCh38.p12 chr3: 119,228,588-119,228,848 B4GALT4, B4GALT4-AS1
    nsv4595991copy number variation2nstd183human GRCh37 chr3: 118,855,337-119,000,251 , GRCh38.p12 chr3: 119,136,490-119,281,404 UPK1B, IGSF11, 3 more genes
    nsv4468313mobile element insertion1nstd166human GRCh37.p13 chr3: 118,945,413-118,945,413 , GRCh38.p12 chr3: 119,226,566-119,226,566 B4GALT4-AS1, B4GALT4
    nsv4467970mobile element insertion1nstd166human GRCh37.p13 chr3: 118,947,673-118,947,673 , GRCh38.p12 chr3: 119,228,826-119,228,826 B4GALT4, B4GALT4-AS1
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