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Items: 1 to 20 of 910

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138131copy number variation1nstd232human GRCh37.p13 chr10: 29,883,209-29,883,263 , GRCh38.p12 chr10: 29,594,280-29,594,334 SVIL
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7076630inversion1nstd229human GRCh38 chr10: 29,313,096-30,347,685 , GRCh37.p13 chr10: 29,602,025-30,636,614 LOC105376475, RNU6-598P, 22 more genes
    nsv7070202inversion1nstd229human GRCh38 chr10: 27,330,033-30,802,827 , GRCh37.p13 chr10: 27,618,962-31,091,756 LINC00837, RPL21P93, 77 more genes
    nsv7058187inversion1nstd229human GRCh38 chr10: 27,002,297-30,809,591 , GRCh37.p13 chr10: 27,291,226-31,098,520 RNU6-490P, LOC105376474, 87 more genes
    nsv6898086copy number variation1nstd229human GRCh38 chr10: 29,729,755-29,736,375 , GRCh37.p13 chr10: 30,018,684-30,025,304 SVIL
    nsv6896210copy number variation1nstd229human GRCh38 chr10: 29,603,201-29,681,900 , GRCh37.p13 chr10: 29,892,130-29,970,829 SVIL
    nsv6895430copy number variation1nstd229human GRCh38 chr10: 29,533,649-29,538,757 , GRCh37.p13 chr10: 29,822,578-29,827,686 SVIL
    nsv6894377copy number variation1nstd229human GRCh38 chr10: 28,466,728-36,061,502 , GRCh37.p13 chr10: 28,755,657-36,350,430 LOC105376482, LOC101929431, 130 more genes
    nsv6894162copy number variation1nstd229human GRCh38 chr10: 29,610,260-29,616,004 , GRCh37.p13 chr10: 29,899,189-29,904,933 SVIL
    nsv6892924copy number variation1nstd229human GRCh38 chr10: 29,711,134-29,711,861 , GRCh37.p13 chr10: 30,000,063-30,000,790 RNU6-908P, SVIL
    nsv6892524copy number variation1nstd229human GRCh38 chr10: 29,591,101-29,599,200 , GRCh37.p13 chr10: 29,880,030-29,888,129 SVIL
    nsv6891841copy number variation1nstd229human GRCh38 chr10: 29,619,481-29,623,426 , GRCh37.p13 chr10: 29,908,410-29,912,355 SVIL
    nsv6891803copy number variation1nstd229human GRCh38 chr10: 29,433,839-29,460,846 , GRCh37.p13 chr10: 29,722,768-29,749,775 SVIL-AS1, SVIL
    nsv6891239copy number variation1nstd229human GRCh38 chr10: 29,560,636-29,561,140 , GRCh37.p13 chr10: 29,849,565-29,850,069 SVIL
    nsv6890786copy number variation1nstd229human GRCh38 chr10: 29,627,761-29,634,139 , GRCh37.p13 chr10: 29,916,690-29,923,068 SVIL
    nsv6890156copy number variation1nstd229human GRCh38 chr10: 29,629,595-29,630,062 , GRCh37.p13 chr10: 29,918,524-29,918,991 SVIL
    nsv6889903copy number variation1nstd229human GRCh38 chr10: 29,610,174-29,619,576 , GRCh37.p13 chr10: 29,899,103-29,908,505 SVIL
    nsv6889299copy number variation1nstd229human GRCh38 chr10: 29,546,001-29,548,700 , GRCh37.p13 chr10: 29,834,930-29,837,629 SVIL
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