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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052094inversion1nstd229human GRCh38 chr3: 132,609,279-139,052,095 , GRCh37.p13 chr3: 132,328,123-138,770,937 RNU6-789P, UBA5, 98 more genes
    nsv7044513inversion1nstd229human GRCh38 chr3: 131,210,998-138,882,695 , GRCh37.p13 chr3: 130,929,842-138,601,537 HSPA8P9, RNU6-1174P, 114 more genes
    nsv7040149inversion1nstd229human GRCh38 chr3: 137,187,995-138,131,845 , GRCh37.p13 chr3: 136,906,837-137,850,687 LINC01210, LOC105374127, 11 more genes
    nsv7039302inversion1nstd229human GRCh38 chr3: 133,378,933-139,551,784 , GRCh37.p13 chr3: 133,097,777-139,270,626 ESYT3, DONSONP1, 99 more genes
    nsv7039034inversion1nstd229human GRCh38 chr3: 136,134,661-138,768,814 , GRCh37.p13 chr3: 135,853,503-138,487,656 KRT8P36, RPL31P23, 37 more genes
    nsv6733058copy number variation1nstd229human GRCh38 chr3: 138,026,905-138,032,772 , GRCh37.p13 chr3: 137,745,747-137,751,614 CLDN18
    nsv6723393copy number variation1nstd229human GRCh38 chr3: 137,996,939-138,101,267 , GRCh37.p13 chr3: 137,715,781-137,820,109 LOC105374128, KRT8P36, 3 more genes
    nsv6722937copy number variation1nstd229human GRCh38 chr3: 136,813,721-138,134,157 , GRCh37.p13 chr3: 136,532,563-137,852,999 LOC105374128, IL20RB-AS1, 17 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6628447copy number variation1nstd224human GRCh37 chr3: 137,717,711-137,748,979 , GRCh38.p12 chr3: 137,998,869-138,030,137 CLDN18, LOC105374127
    nsv6364787copy number variation1nstd223human GRCh38 chr3: 137,990,378-138,008,195 , GRCh37.p13 chr3: 137,709,220-137,727,037 CLDN18
    nsv6289867copy number variation1nstd102humanUncertain significance GRCh37 chr3: 137,727,844-137,778,355 , GRCh38.p12 chr3: 138,009,002-138,059,513 CLDN18, LOC105374127, 1 more genes
    nsv6134785copy number variation1nstd213human GRCh37 chr3: 135,840,000-139,360,001 , GRCh38.p12 chr3: 136,121,158-139,641,159 ACTG1P1, FOXL2, 59 more genes
    nsv5889866copy number variation1nstd209human GRCh38 chr3: 137,097,814-139,588,879 , GRCh37.p13 chr3: 136,816,656-139,307,721 , LOC105374127, 42 more genes
    nsv5834677copy number variation1nstd209human GRCh38 chr3: 138,005,972-138,007,771 , GRCh37.p13 chr3: 137,724,814-137,726,613 CLDN18
    nsv5834329copy number variation1nstd209human GRCh38 chr3: 137,989,496-138,007,771 , GRCh37.p13 chr3: 137,708,338-137,726,613 CLDN18
    nsv5676538mobile element insertion1nstd211human GRCh38 chr3: 138,004,542-138,004,542 , GRCh37.p13 chr3: 137,723,384-137,723,384 CLDN18
    nsv5403762mobile element insertion1nstd206human GRCh38 chr3: 138,004,542-138,004,593 , GRCh37.p13 chr3: 137,723,384-137,723,435 CLDN18
    nsv5099799mobile element insertion1nstd203human GRCh38 chr3: 138,033,474-138,033,488 , GRCh37.p13 chr3: 137,752,316-137,752,330 CLDN18
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
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