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Items: 1 to 20 of 295

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124566insertion1nstd186human GRCh37 chr7: 26,351,486-26,351,486 , GRCh38.p12 chr7: 26,311,866-26,311,866 SNX10
    nsv5959433insertion1nstd209human GRCh38 chr7: 26,311,855-26,311,855 , GRCh37.p13 chr7: 26,351,475-26,351,475 SNX10
    nsv5909256copy number variation1nstd209human GRCh38 chr7: 26,331,769-26,344,208 , GRCh37.p13 chr7: 26,371,389-26,383,828 SNX10
    nsv5846910copy number variation2nstd209human GRCh38 chr7: 26,334,129-26,335,528 , GRCh37.p13 chr7: 26,373,749-26,375,148 SNX10
    nsv5846211copy number variation1nstd209human GRCh38 chr7: 26,331,729-26,335,378 , GRCh37.p13 chr7: 26,371,349-26,374,998 SNX10
    nsv5692915mobile element insertion2nstd211human GRCh38 chr7: 26,311,869-26,311,869 , GRCh37.p13 chr7: 26,351,489-26,351,489 SNX10
    nsv5673846copy number variation1nstd102humanPathogenic GRCh37 chr7: 26,400,575-26,404,785 , GRCh38.p12 chr7: 26,360,955-26,365,165 SNX10
    nsv5629260insertion1nstd207human GRCh38 chr7: 26,311,866-26,311,866 , GRCh37.p13 chr7: 26,351,486-26,351,486 SNX10
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5551789insertion1nstd206human GRCh38 chr7: 26,291,957-26,291,973 , GRCh37.p13 chr7: 26,331,577-26,331,593 SNX10
    nsv5538733insertion1nstd206human GRCh38 chr7: 26,311,866-26,311,866 , GRCh37.p13 chr7: 26,351,486-26,351,486 SNX10
    nsv5493252copy number variation1nstd206human GRCh38 chr7: 26,290,462-26,320,723 , GRCh37.p13 chr7: 26,330,082-26,360,343 SNX10
    nsv5490811copy number variation1nstd206human GRCh38 chr7: 26,312,478-26,313,933 , GRCh37.p13 chr7: 26,352,098-26,353,553 SNX10
    nsv5370466translocation1nstd200human GRCh38 chr7: 26,320,116-26,320,116 , GRCh38 chr7: 26,321,868-26,321,868 , GRCh37.p13 chr7: 26,361,488-26,361,488 , GRCh37.p13 chr7: 26,359,736-26,359,736 SNX10
    nsv5370465translocation1nstd200human GRCh38 chr7: 26,313,933-26,313,933 , GRCh38 chr7: 26,312,478-26,312,478 , GRCh37.p13 chr7: 26,352,098-26,352,098 , GRCh37.p13 chr7: 26,353,553-26,353,553 SNX10
    nsv5339739translocation1nstd200human GRCh37 chr7: 26,352,098-26,352,098 , GRCh37 chr7: 26,353,553-26,353,553 , GRCh38.p12 chr7: 26,312,478-26,312,478 , GRCh38.p12 chr7: 26,313,933-26,313,933 SNX10
    nsv5181350mobile element insertion1nstd203human GRCh38 chr7: 26,356,852-26,356,864 , GRCh37.p13 chr7: 26,396,472-26,396,484 SNX10
    nsv5118107mobile element insertion1nstd203human GRCh38 chr7: 26,311,861-26,311,869 , GRCh37.p13 chr7: 26,351,481-26,351,489 SNX10
    nsv5116840mobile element insertion1nstd203human GRCh38 chr7: 26,311,856-26,311,869 , GRCh37.p13 chr7: 26,351,476-26,351,489 SNX10
    nsv5115901mobile element insertion1nstd203human GRCh38 chr7: 26,314,994-26,315,009 , GRCh37.p13 chr7: 26,354,614-26,354,629 SNX10
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