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Items: 1 to 20 of 450

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv6129481mobile element insertion1nstd186human GRCh37 chr21: 17,134,461-17,134,512 , GRCh38.p12 chr21: 15,762,142-15,762,193 USP25
    nsv5977628insertion1nstd209human GRCh38 chr21: 15,762,129-15,762,129 , GRCh37.p13 chr21: 17,134,448-17,134,448 USP25
    nsv5965857copy number variation1nstd209human GRCh38 chr21: 14,377,888-22,678,896 , GRCh37.p13 chr21: 15,750,209-24,051,216 , LOC107985508, 80 more genes
    nsv5961944copy number variation1nstd209human GRCh38 chr21: 15,744,366-15,744,627 , GRCh37.p13 chr21: 17,116,685-17,116,946 USP25, RBPMSLP
    nsv5720216mobile element insertion2nstd211human GRCh38 chr21: 15,762,142-15,762,142 , GRCh37.p13 chr21: 17,134,461-17,134,461 USP25
    nsv5712040mobile element insertion1nstd211human GRCh38 chr21: 15,854,985-15,854,985 , GRCh37.p13 chr21: 17,227,304-17,227,304 USP25
    nsv5702877mobile element insertion2nstd211human GRCh38 chr21: 15,842,242-15,842,242 , GRCh37.p13 chr21: 17,214,561-17,214,561 USP25
    nsv5702559mobile element insertion1nstd211human GRCh38 chr21: 15,751,233-15,751,233 , GRCh37.p13 chr21: 17,123,552-17,123,552 USP25
    nsv5670715insertion1nstd207human GRCh38 chr21: 15,762,129-15,762,129 , GRCh37.p13 chr21: 17,134,448-17,134,448 USP25
    nsv5670064insertion1nstd207human GRCh38 chr21: 15,740,673-15,740,673 , GRCh37.p13 chr21: 17,112,992-17,112,992 USP25
    nsv5666883insertion1nstd207human GRCh38 chr21: 15,836,926-15,836,926 , GRCh37.p13 chr21: 17,209,245-17,209,245 USP25
    nsv5602046copy number variation1nstd207human GRCh38 chr21: 15,836,926-15,837,007 , GRCh37.p13 chr21: 17,209,245-17,209,326 USP25
    nsv5585474copy number variation1nstd207human GRCh38 chr21: 15,836,874-15,837,119 , GRCh37.p13 chr21: 17,209,193-17,209,438 USP25
    nsv5554416mobile element insertion1nstd206human GRCh38 chr21: 15,762,142-15,762,193 , GRCh37.p13 chr21: 17,134,461-17,134,512 USP25
    nsv5539790insertion1nstd206human GRCh38 chr21: 5,227,438-39,583,816 , GRCh37.p13 chr21: 10,697,897-44,966,043 , LOC100419041, 557 more genes
    nsv5518921copy number variation1nstd206human GRCh38 chr21: 15,836,748-15,837,442 , GRCh37.p13 chr21: 17,209,067-17,209,761 USP25
    nsv5514204copy number variation1nstd206human GRCh38 chr21: 15,842,207-15,842,350 , GRCh37.p13 chr21: 17,214,526-17,214,669 USP25
    nsv5425363mobile element insertion1nstd206human GRCh38 chr21: 15,751,233-15,751,284 , GRCh37.p13 chr21: 17,123,552-17,123,603 USP25
    nsv5423183mobile element insertion1nstd206human GRCh38 chr21: 15,854,985-15,855,036 , GRCh37.p13 chr21: 17,227,304-17,227,355 USP25
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