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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095898copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,223,339-44,638,757 , GRCh38.p12 chr20: 43,594,699-46,010,118 ADA, CCN5, 99 more genes
    nsv7075825inversion1nstd229human GRCh38 chr20: 45,232,922-45,712,689 , GRCh37.p13 chr20: 43,861,563-44,341,328 PIGT, LOC105372630, 33 more genes
    nsv7028861copy number variation1nstd229human GRCh38 chr20: 45,663,583-45,669,422 , GRCh37.p13 chr20: 44,292,222-44,298,061 WFDC11
    nsv7025925copy number variation1nstd229human GRCh38 chr20: 45,651,401-45,665,700 , GRCh37.p13 chr20: 44,280,040-44,294,339 WFDC11
    nsv6552592copy number variation1nstd223human GRCh38 chr20: 45,637,501-45,647,100 , GRCh37.p13 chr20: 44,266,140-44,275,739 RPS2P7, WFDC11
    nsv6290315copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,985,044-48,599,046 , GRCh38.p12 chr20: 44,356,404-49,982,509 PABPC1L, LOC107985401, 170 more genes
    nsv6289696insertion1nstd214human GRCh38 chr20: 45,651,763-45,651,763 , GRCh37.p13 chr20: 44,280,402-44,280,402 WFDC11
    nsv6134034copy number variation1nstd213human GRCh37 chr20: 44,070,000-44,320,001 , GRCh38.p12 chr20: 45,441,360-45,691,362 EPPIN, RPL5P2, 15 more genes
    nsv6133816copy number variation1nstd213human GRCh37 chr20: 43,650,000-45,170,001 , GRCh38.p12 chr20: 45,021,359-46,541,362 MMP9, PI3, 76 more genes
    nsv5671837insertion1nstd207human GRCh38 chr20: 45,651,763-45,651,763 , GRCh37.p13 chr20: 44,280,402-44,280,402 WFDC11
    nsv5183058mobile element insertion1nstd203human GRCh38 chr20: 45,652,843-45,652,856 , GRCh37.p13 chr20: 44,281,482-44,281,495 WFDC11
    nsv5178189mobile element insertion1nstd203human GRCh38 chr20: 45,669,713-45,669,727 , GRCh37.p13 chr20: 44,298,352-44,298,366 WFDC11
    nsv5172061mobile element insertion1nstd203human GRCh38 chr20: 45,656,916-45,656,931 , GRCh37.p13 chr20: 44,285,555-44,285,570 WFDC11
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv5012840copy number variation1nstd200human GRCh38 chr20: 45,659,749-45,661,402 , GRCh37.p13 chr20: 44,288,388-44,290,041 WFDC11
    nsv4868593copy number variation1nstd200human GRCh37 chr20: 31,164,049-45,167,425 , GRCh38.p12 chr20: 32,576,247-46,538,786 , MMP24-AS1-EDEM2, 350 more genes
    nsv4853668copy number variation1nstd200human GRCh37 chr20: 44,288,388-44,290,041 , GRCh38.p12 chr20: 45,659,749-45,661,402 WFDC11
    nsv4853667copy number variation1nstd200human GRCh37 chr20: 44,287,800-44,289,517 , GRCh38.p12 chr20: 45,659,161-45,660,878 WFDC11
    nsv4674805copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 34,980,430-46,806,549 , GRCh38.p12 chr20: 36,352,027-48,177,806 ADA, BPI, 266 more genes
    nsv4641390copy number variation1nstd186human GRCh37 chr20: 44,280,402-44,280,457 , GRCh38.p12 chr20: 45,651,763-45,651,818 WFDC11
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