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Items: 1 to 20 of 475

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115708mobile element insertion1nstd186human GRCh37 chr12: 76,823,043-76,823,043 , GRCh38.p12 chr12: 76,429,263-76,429,263 OSBPL8
    nsv5969238insertion1nstd209human GRCh38 chr12: 76,429,263-76,429,263 , GRCh37.p13 chr12: 76,823,043-76,823,043 OSBPL8
    nsv5941783copy number variation1nstd209human GRCh38 chr12: 76,379,030-76,381,977 , GRCh37.p13 chr12: 76,772,810-76,775,757 OSBPL8
    nsv5937623copy number variation1nstd209human GRCh38 chr12: 76,506,919-76,508,031 , GRCh37.p13 chr12: 76,900,699-76,901,811 OSBPL8
    nsv5864429copy number variation1nstd209human GRCh38 chr12: 76,379,054-76,381,453 , GRCh37.p13 chr12: 76,772,834-76,775,233 OSBPL8
    nsv5858485copy number variation1nstd209human GRCh38 chr12: 76,506,927-76,508,067 , GRCh37.p13 chr12: 76,900,707-76,901,847 OSBPL8
    nsv5854589copy number variation2nstd209human GRCh38 chr12: 76,496,574-76,497,573 , GRCh37.p13 chr12: 76,890,354-76,891,353 OSBPL8
    nsv5730209mobile element insertion1nstd211human GRCh38 chr12: 76,405,478-76,405,478 , GRCh37.p13 chr12: 76,799,258-76,799,258 OSBPL8
    nsv5724422mobile element insertion1nstd211human GRCh38 chr12: 76,391,976-76,391,976 , GRCh37.p13 chr12: 76,785,756-76,785,756 OSBPL8
    nsv5707487mobile element insertion1nstd211human GRCh38 chr12: 76,539,075-76,539,075 , GRCh37.p13 chr12: 76,932,855-76,932,855 OSBPL8
    nsv5704654mobile element insertion2nstd211human GRCh38 chr12: 76,411,517-76,411,517 , GRCh37.p13 chr12: 76,805,297-76,805,297 OSBPL8
    nsv5703983mobile element insertion1nstd211human GRCh38 chr12: 76,398,080-76,398,080 , GRCh37.p13 chr12: 76,791,860-76,791,860 OSBPL8
    nsv5703868mobile element insertion2nstd211human GRCh38 chr12: 76,429,278-76,429,278 , GRCh37.p13 chr12: 76,823,058-76,823,058 OSBPL8
    nsv5703840mobile element insertion2nstd211human GRCh38 chr12: 76,556,306-76,556,306 , GRCh37.p13 chr12: 76,950,086-76,950,086 OSBPL8
    nsv5651376insertion1nstd207human GRCh38 chr12: 76,411,500-76,411,500 , GRCh37.p13 chr12: 76,805,280-76,805,280 OSBPL8
    nsv5648659insertion1nstd207human GRCh38 chr12: 76,429,263-76,429,263 , GRCh37.p13 chr12: 76,823,043-76,823,043 OSBPL8
    nsv5599769copy number variation1nstd207human GRCh38 chr12: 76,506,918-76,508,028 , GRCh37.p13 chr12: 76,900,698-76,901,808 OSBPL8
    nsv5563970sequence alteration1nstd206human GRCh38 chr12: 76,420,062-76,420,063 , GRCh37.p13 chr12: 76,813,842-76,813,843 OSBPL8
    nsv5511492copy number variation1nstd206human GRCh38 chr12: 76,506,919-76,508,032 , GRCh37.p13 chr12: 76,900,699-76,901,812 OSBPL8
    nsv5509253copy number variation1nstd206human GRCh38 chr12: 76,441,864-76,444,813 , GRCh37.p13 chr12: 76,835,644-76,838,593 OSBPL8
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