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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940786copy number variation1nstd209human GRCh38 chr19: 10,369,981-10,370,450 , GRCh37.p13 chr19: 10,480,657-10,481,126 TYK2
    nsv5664151insertion1nstd207human GRCh38 chr19: 10,361,635-10,361,635 , GRCh37.p13 chr19: 10,472,311-10,472,311 TYK2
    nsv5650909insertion1nstd207human GRCh38 chr19: 10,377,665-10,377,665 , GRCh37.p13 chr19: 10,488,341-10,488,341 TYK2
    nsv5533888copy number variation1nstd206human GRCh38 chr19: 10,358,873-10,359,828 , GRCh37.p13 chr19: 10,469,549-10,470,504 TYK2
    nsv5527824copy number variation1nstd206human GRCh38 chr19: 10,370,132-10,371,467 , GRCh37.p13 chr19: 10,480,808-10,482,143 TYK2
    nsv5522778copy number variation1nstd206human GRCh38 chr19: 10,375,341-10,376,645 , GRCh37.p13 chr19: 10,486,017-10,487,321 TYK2
    nsv5519889copy number variation1nstd206human GRCh38 chr19: 10,372,205-10,388,807 , GRCh37.p13 chr19: 10,482,881-10,499,483 TYK2
    nsv5514959copy number variation1nstd206human GRCh38 chr19: 10,369,981-10,370,093 , GRCh37.p13 chr19: 10,480,657-10,480,769 TYK2
    nsv5335828translocation1nstd200human GRCh37 chr19: 10,467,508-10,467,508 , GRCh37 chr19: 10,467,442-10,467,442 , GRCh38.p12 chr19: 10,356,766-10,356,766 , GRCh38.p12 chr19: 10,356,832-10,356,832 TYK2
    nsv5295515copy number variation1nstd204human GRCh38.p13 chr19: 10,379,410-10,382,603 , GRCh37.p13 chr19: 10,490,086-10,493,279 TYK2
    nsv5291380copy number variation1nstd204human GRCh38.p13 chr19: 10,335,201-10,670,200 , GRCh37.p13 chr19: 10,445,877-10,780,876 ICAM3, MIR1181, 15 more genes
    nsv5287330copy number variation1nstd204human GRCh38.p13 chr19: 10,335,601-11,755,400 , GRCh37.p13 chr19: 10,446,277-11,866,215 AP1M2, C19orf38, 64 more genes
    nsv5284675copy number variation1nstd204human GRCh38.p13 chr19: 10,375,668-10,380,453 , GRCh37.p13 chr19: 10,486,344-10,491,129 TYK2
    nsv5281427copy number variation1nstd204human GRCh38.p13 chr19: 10,376,101-10,382,200 , GRCh37.p13 chr19: 10,486,777-10,492,876 TYK2
    nsv5014505copy number variation1nstd200human GRCh38 chr19: 10,370,084-10,371,473 , GRCh37.p13 chr19: 10,480,760-10,482,149 TYK2
    nsv5011609copy number variation1nstd200human GRCh38 chr19: 10,375,340-10,376,645 , GRCh37.p13 chr19: 10,486,016-10,487,321 TYK2
    nsv5011608copy number variation1nstd200human GRCh38 chr19: 10,347,542-10,350,151 , GRCh37.p13 chr19: 10,458,218-10,460,827 TYK2
    nsv4864917copy number variation1nstd200human GRCh37 chr19: 10,486,910-10,505,533 , GRCh38.p12 chr19: 10,376,234-10,394,857 CDC37, TYK2
    nsv4852985copy number variation1nstd200human GRCh37 chr19: 10,458,246-10,460,800 , GRCh38.p12 chr19: 10,347,570-10,350,124 TYK2
    nsv4753359insertion1nstd199human GRCh37 chr19: 10,488,308-10,488,308 , GRCh38.p12 chr19: 10,377,632-10,377,632 TYK2
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