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Items: 1 to 20 of 198

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5523587copy number variation1nstd206human GRCh38 chr20: 33,435,349-33,435,990 , GRCh37.p13 chr20: 32,023,155-32,023,796 SNTA1
    nsv5381306copy number variation1nstd102humanUncertain significance GRCh37 chr20: 32,026,637-32,031,436 , GRCh38.p12 chr20: 33,438,831-33,443,630 SNTA1
    nsv5025522copy number variation1nstd200human GRCh38 chr20: 33,431,441-33,461,985 , GRCh37.p13 chr20: 32,019,247-32,049,791 SNTA1
    nsv5025521copy number variation1nstd200human GRCh38 chr20: 33,426,450-33,460,292 , GRCh37.p13 chr20: 32,014,256-32,048,098 SNTA1
    nsv5025520copy number variation1nstd200human GRCh38 chr20: 33,371,456-33,468,046 , GRCh37.p13 chr20: 31,959,262-32,055,852 CDK5RAP1, SNTA1
    nsv5025519copy number variation1nstd200human GRCh38 chr20: 33,313,823-33,665,851 , GRCh37.p13 chr20: 31,901,629-32,253,657 CBFA2T2, C20orf144, 6 more genes
    nsv5022343copy number variation1nstd200human GRCh38 chr20: 32,602,560-45,347,064 , GRCh37.p13 chr20: 31,190,362-43,975,704 , SNHG11, 286 more genes
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv5022326copy number variation1nstd200human GRCh38 chr20: 32,216,214-44,981,731 , GRCh37.p13 chr20: 30,804,017-43,610,372 , HNF4A, 279 more genes
    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
    nsv4868578copy number variation1nstd200human GRCh37 chr20: 30,804,017-43,610,372 , GRCh38.p12 chr20: 32,216,214-44,981,731 , SNORA71C, 279 more genes
    nsv4865529copy number variation1nstd200human GRCh37 chr20: 31,959,223-32,055,949 , GRCh38.p12 chr20: 33,371,417-33,468,143 CDK5RAP1, SNTA1
    nsv4676132copy number variation1nstd102humanUncertain significance GRCh37 chr20: 31,966,407-33,169,058 , GRCh38.p12 chr20: 33,378,601-34,581,254 MAP1LC3A, PXMP4, 28 more genes
    nsv4627471copy number variation1nstd183human GRCh37 chr20: 31,936,199-32,187,796 , GRCh38.p12 chr20: 33,348,393-33,599,990 CDK5RAP1, BPIFB9P, 2 more genes
    nsv4511028mobile element insertion1nstd166human GRCh37.p13 chr20: 32,028,853-32,028,853 , GRCh38.p12 chr20: 33,441,047-33,441,047 SNTA1
    nsv4457806copy number variation1nstd102humanPathogenic GRCh37 chr20: 29,833,608-35,087,952 , GRCh38.p12 chr20: 31,245,805-36,459,549 EFCAB8, C20orf203, 162 more genes
    nsv4288788copy number variation1nstd166human GRCh37.p13 chr20: 32,016,900-32,025,000 , GRCh38.p12 chr20: 33,429,094-33,437,194 SNTA1
    nsv4281129copy number variation1nstd166human GRCh37.p13 chr20: 32,008,683-32,009,311 , GRCh38.p12 chr20: 33,420,877-33,421,505 SNTA1
    nsv4280066copy number variation1nstd166human GRCh37.p13 chr20: 31,997,348-32,149,306 , GRCh38.p12 chr20: 33,409,542-33,561,500 SNTA1, CBFA2T2
    nsv4277571copy number variation1nstd166human GRCh37.p13 chr20: 31,959,317-32,055,799 , GRCh38.p12 chr20: 33,371,511-33,467,993 SNTA1, CDK5RAP1
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