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Items: 1 to 20 of 138

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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
    nsv7062736inversion1nstd229human GRCh38 chr20: 36,955,253-45,585,462 , GRCh37.p13 chr20: 35,583,656-44,214,101 GDAP1L1, PI3, 177 more genes
    nsv7029276copy number variation1nstd229human GRCh38 chr20: 45,102,905-45,108,658 , GRCh37.p13 chr20: 43,731,546-43,737,299 WFDC5
    nsv7026053copy number variation1nstd229human GRCh38 chr20: 45,114,392-45,114,543 , GRCh37.p13 chr20: 43,743,033-43,743,184 WFDC5
    nsv7025630copy number variation1nstd229human GRCh38 chr20: 45,115,084-45,130,231 , GRCh37.p13 chr20: 43,743,725-43,758,872 WFDC12, WFDC5
    nsv6596116inversion1nstd223human GRCh38 chr20: 36,955,253-45,585,469 , GRCh37.p13 chr20: 35,583,656-44,214,108 LOC101929863, LOC105372620, 177 more genes
    nsv6536972copy number variation1nstd223human GRCh38 chr20: 45,102,905-45,108,657 , GRCh37.p13 chr20: 43,731,546-43,737,298 WFDC5
    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
    nsv6227026copy number variation1nstd214human GRCh38 chr20: 45,113,797-45,113,942 , GRCh37.p13 chr20: 43,742,438-43,742,583 WFDC5
    nsv6134164copy number variation1nstd213human GRCh37 chr20: 43,170,000-44,070,001 , GRCh38.p12 chr20: 44,541,359-45,441,361 PI3, SEMG2, 35 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
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5970115insertion1nstd209human GRCh38 chr20: 45,116,613-45,116,613 , GRCh37.p13 chr20: 43,745,254-43,745,254 WFDC5
    nsv5324090inversion1nstd204human GRCh37.p13 chr20: 35,583,652-44,214,109 , GRCh38.p13 chr20: 36,955,249-45,585,470 , BPI, 180 more genes
    nsv5172722mobile element insertion1nstd203human GRCh38 chr20: 45,116,612-45,116,612 , GRCh37.p13 chr20: 43,745,253-43,745,253 WFDC5
    nsv5169522mobile element insertion1nstd203human GRCh38 chr20: 45,116,541-45,116,541 , GRCh37.p13 chr20: 43,745,182-43,745,182 WFDC5
    nsv5166775mobile element insertion1nstd203human GRCh38 chr20: 45,116,564-45,116,564 , GRCh37.p13 chr20: 43,745,205-43,745,205 WFDC5
    nsv5033948inversion1nstd200human GRCh38 chr20: 36,955,253-45,585,464 , GRCh37.p13 chr20: 35,583,656-44,214,103 , EMILIN3, 180 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
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