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Items: 1 to 20 of 237

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965604insertion1nstd209human GRCh38 chr3: 185,592,011-185,592,011 , GRCh37.p13 chr3: 185,309,799-185,309,799 SENP2
    nsv5948726insertion1nstd209human GRCh38 chr3: 185,587,570-185,587,570 , GRCh37.p13 chr3: 185,305,358-185,305,358 SENP2
    nsv5895485copy number variation1nstd209human GRCh38 chr3: 185,632,478-185,632,766 , GRCh37.p13 chr3: 185,350,266-185,350,554 SENP2
    nsv5895026copy number variation1nstd209human GRCh38 chr3: 185,627,663-185,628,757 , GRCh37.p13 chr3: 185,345,451-185,346,545 SENP2
    nsv5835705copy number variation1nstd209human GRCh38 chr3: 185,633,042-185,656,158 , GRCh37.p13 chr3: 185,350,830-185,373,946 IGF2BP2, SENP2
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5449864copy number variation1nstd206human GRCh38 chr3: 185,601,265-185,601,858 , GRCh37.p13 chr3: 185,319,053-185,319,646 SENP2
    nsv5449086copy number variation1nstd206human GRCh38 chr3: 185,591,174-185,592,821 , GRCh37.p13 chr3: 185,308,962-185,310,609 SENP2
    nsv5447866copy number variation1nstd206human GRCh38 chr3: 185,607,512-185,607,585 , GRCh37.p13 chr3: 185,325,300-185,325,373 SENP2
    nsv5443723copy number variation1nstd206human GRCh38 chr3: 185,629,000-185,629,101 , GRCh37.p13 chr3: 185,346,788-185,346,889 SENP2
    nsv5438339copy number variation1nstd206human GRCh38 chr3: 185,571,100-185,625,574 , GRCh37.p13 chr3: 185,288,888-185,343,362 RPL34P10, SENP2
    nsv5308583copy number variation1nstd204human GRCh38.p13 chr3: 185,591,162-185,592,808 , GRCh37.p13 chr3: 185,308,950-185,310,596 SENP2
    nsv5193653mobile element insertion1nstd203human GRCh38 chr3: 185,613,990-185,614,001 , GRCh37.p13 chr3: 185,331,778-185,331,789 SENP2
    nsv5098431mobile element insertion1nstd203human GRCh38 chr3: 185,588,038-185,588,050 , GRCh37.p13 chr3: 185,305,826-185,305,838 SENP2
    nsv5085725mobile element insertion1nstd203human GRCh38 chr3: 185,601,951-185,601,965 , GRCh37.p13 chr3: 185,319,739-185,319,753 SENP2
    nsv5085462mobile element insertion1nstd203human GRCh38 chr3: 185,599,711-185,599,723 , GRCh37.p13 chr3: 185,317,499-185,317,511 SENP2
    nsv5083509mobile element insertion1nstd203human GRCh38 chr3: 185,634,031-185,634,041 , GRCh37.p13 chr3: 185,351,819-185,351,829 SENP2
    nsv4924959copy number variation1nstd200human GRCh38 chr3: 185,596,142-185,598,026 , GRCh37.p13 chr3: 185,313,930-185,315,814 SENP2
    nsv4924957copy number variation1nstd200human GRCh38 chr3: 185,541,868-185,592,859 , GRCh37.p13 chr3: 185,259,656-185,310,647 , SENP2, 1 more genes
    nsv4924956copy number variation1nstd200human GRCh38 chr3: 185,453,868-185,804,751 , GRCh37.p13 chr3: 185,171,656-185,522,539 , LIPH, 9 more genes
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