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Items: 1 to 20 of 840

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5954870insertion1nstd209human GRCh38 chr3: 8,987,642-8,987,642 , GRCh37.p13 chr3: 9,029,326-9,029,326 SRGAP3
    nsv5904753copy number variation1nstd209human GRCh38 chr3: 9,077,373-9,077,431 , GRCh37.p13 chr3: 9,119,057-9,119,115 SRGAP3
    nsv5896948copy number variation1nstd209human GRCh38 chr3: 9,235,693-9,242,538 , GRCh37.p13 chr3: 9,277,377-9,284,222 SRGAP3
    nsv5896642copy number variation1nstd209human GRCh38 chr3: 9,212,489-9,212,582 , GRCh37.p13 chr3: 9,254,173-9,254,266 SRGAP3
    nsv5893995copy number variation1nstd209human GRCh38 chr3: 9,086,726-9,086,804 , GRCh37.p13 chr3: 9,128,410-9,128,488 SRGAP3
    nsv5892284copy number variation1nstd209human GRCh38 chr3: 9,283,869-9,290,191 , GRCh37.p13 chr3: 9,325,553-9,331,875 SRGAP3
    nsv5888259copy number variation1nstd209human GRCh38 chr3: 9,353,884-9,354,088 , GRCh37.p13 chr3: 9,395,568-9,395,772 SRGAP3
    nsv5837230copy number variation1nstd209human GRCh38 chr3: 9,235,093-9,242,505 , GRCh37.p13 chr3: 9,276,777-9,284,189 SRGAP3
    nsv5837181copy number variation1nstd209human GRCh38 chr3: 9,283,833-9,290,181 , GRCh37.p13 chr3: 9,325,517-9,331,865 SRGAP3
    nsv5719119mobile element insertion1nstd211human GRCh38 chr3: 9,031,874-9,031,874 , GRCh37.p13 chr3: 9,073,558-9,073,558 SRGAP3
    nsv5689969mobile element insertion1nstd211human GRCh38 chr3: 9,145,953-9,145,953 , GRCh37.p13 chr3: 9,187,637-9,187,637 SRGAP3
    nsv5689128mobile element insertion2nstd211human GRCh38 chr3: 9,320,954-9,320,954 , GRCh37.p13 chr3: 9,362,638-9,362,638 SRGAP3
    nsv5676209mobile element insertion1nstd211human GRCh38 chr3: 9,243,875-9,243,875 , GRCh37.p13 chr3: 9,285,559-9,285,559 SRGAP3
    nsv5620304insertion1nstd207human GRCh38 chr3: 9,300,174-9,300,174 , GRCh37.p13 chr3: 9,341,858-9,341,858 SRGAP3
    nsv5611661insertion1nstd207human GRCh38 chr3: 8,987,642-8,987,642 , GRCh37.p13 chr3: 9,029,326-9,029,326 SRGAP3
    nsv5604539insertion1nstd207human GRCh38 chr3: 9,086,726-9,086,726 , GRCh37.p13 chr3: 9,128,410-9,128,410 SRGAP3
    nsv5574124copy number variation1nstd207human GRCh38 chr3: 9,212,489-9,212,582 , GRCh37.p13 chr3: 9,254,173-9,254,266 SRGAP3
    nsv5557885sequence alteration1nstd206human GRCh37.p13 chr3: 9,254,033-9,464,050 , GRCh38 chr3: 9,212,349-9,422,366 SRGAP3, THUMPD3, 5 more genes
    nsv5539658insertion1nstd206human GRCh38 chr3: 8,987,660-8,987,693 , GRCh37.p13 chr3: 9,029,344-9,029,377 SRGAP3
    nsv5453427copy number variation1nstd206human GRCh38 chr3: 9,180,775-9,183,520 , GRCh37.p13 chr3: 9,222,459-9,225,204 SRGAP3
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