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Items: 1 to 20 of 359

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960448insertion1nstd209human GRCh38 chr9: 115,095,456-115,095,456 , GRCh37.p13 chr9: 117,857,735-117,857,735 TNC
    nsv5709198mobile element insertion2nstd211human GRCh38 chr9: 115,073,178-115,073,178 , GRCh37.p13 chr9: 117,835,457-117,835,457 TNC
    nsv5706175mobile element insertion1nstd211human GRCh38 chr9: 115,095,555-115,095,555 , GRCh37.p13 chr9: 117,857,834-117,857,834 TNC
    nsv5696293mobile element insertion1nstd211human GRCh38 chr9: 115,077,666-115,077,666 , GRCh37.p13 chr9: 117,839,945-117,839,945 TNC
    nsv5636075insertion1nstd207human GRCh38 chr9: 115,095,598-115,095,598 , GRCh37.p13 chr9: 117,857,877-117,857,877 TNC
    nsv5635119insertion1nstd207human GRCh38 chr9: 115,069,662-115,069,662 , GRCh37.p13 chr9: 117,831,941-117,831,941 TNC
    nsv5600552copy number variation1nstd207human GRCh38 chr9: 115,069,666-115,069,725 , GRCh37.p13 chr9: 117,831,945-117,832,004 TNC
    nsv5589564copy number variation1nstd207human GRCh38 chr9: 115,095,450-115,095,607 , GRCh37.p13 chr9: 117,857,729-117,857,886 TNC
    nsv5491051copy number variation1nstd206human GRCh38 chr9: 115,077,316-115,077,478 , GRCh37.p13 chr9: 117,839,595-117,839,757 TNC
    nsv5487310copy number variation1nstd206human GRCh38 chr9: 115,095,491-115,095,672 , GRCh37.p13 chr9: 117,857,770-117,857,951 TNC
    nsv5400630mobile element insertion1nstd206human GRCh38 chr9: 115,073,178-115,073,229 , GRCh37.p13 chr9: 117,835,457-117,835,508 TNC
    nsv5332700translocation1nstd200human GRCh37 chr9: 117,877,022-117,877,022 , GRCh37 chr9: 117,876,861-117,876,861 , GRCh38.p12 chr9: 115,114,582-115,114,582 , GRCh38.p12 chr9: 115,114,743-115,114,743 TNC
    nsv5136643mobile element insertion1nstd203human GRCh38 chr9: 115,033,968-115,033,978 , GRCh37.p13 chr9: 117,796,247-117,796,257 TNC
    nsv5133474mobile element insertion1nstd203human GRCh38 chr9: 115,080,755-115,080,761 , GRCh37.p13 chr9: 117,843,034-117,843,040 TNC
    nsv5121602mobile element insertion1nstd203human GRCh38 chr9: 115,055,649-115,055,660 , GRCh37.p13 chr9: 117,817,928-117,817,939 TNC
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983317copy number variation1nstd200human GRCh38 chr9: 115,111,916-115,111,990 , GRCh37.p13 chr9: 117,874,195-117,874,269 TNC
    nsv4983316copy number variation1nstd200human GRCh38 chr9: 115,098,241-115,098,324 , GRCh37.p13 chr9: 117,860,520-117,860,603 TNC
    nsv4983315copy number variation1nstd200human GRCh38 chr9: 115,086,716-115,086,800 , GRCh37.p13 chr9: 117,848,995-117,849,079 TNC
    nsv4983314copy number variation1nstd200human GRCh38 chr9: 115,077,345-115,077,450 , GRCh37.p13 chr9: 117,839,624-117,839,729 TNC
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