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Items: 1 to 20 of 209

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5963986copy number variation1nstd209human GRCh38 chr20: 44,646,459-44,649,664 , GRCh37.p13 chr20: 43,275,100-43,278,305 ADA
    nsv5952449copy number variation1nstd209human GRCh38 chr20: 44,635,940-44,635,994 , GRCh37.p13 chr20: 43,264,581-43,264,635 ADA
    nsv5871042copy number variation1nstd209human GRCh38 chr20: 44,646,486-44,649,610 , GRCh37.p13 chr20: 43,275,127-43,278,251 ADA
    nsv5673418copy number variation1nstd102humanPathogenic GRCh37 chr20: 43,264,848-43,264,949 , GRCh38.p12 chr20: 44,636,207-44,636,308 ADA
    nsv5673178copy number variation1nstd102humanPathogenic GRCh37 chr20: 43,252,823-43,255,260 , GRCh38.p12 chr20: 44,624,182-44,626,619 ADA
    nsv5601352copy number variation1nstd207human GRCh38 chr20: 44,646,459-44,649,664 , GRCh37.p13 chr20: 43,275,100-43,278,305 ADA
    nsv5521152copy number variation1nstd206human GRCh38 chr20: 44,635,941-44,635,995 , GRCh37.p13 chr20: 43,264,582-43,264,636 ADA
    nsv5514910copy number variation1nstd206human GRCh38 chr20: 44,646,439-44,649,686 , GRCh37.p13 chr20: 43,275,080-43,278,327 ADA
    nsv5324090inversion1nstd204human GRCh37.p13 chr20: 35,583,652-44,214,109 , GRCh38.p13 chr20: 36,955,249-45,585,470 , BPI, 180 more genes
    nsv5324033copy number variation1nstd204human GRCh38.p13 chr20: 44,646,453-44,649,685 , GRCh37.p13 chr20: 43,275,094-43,278,326 ADA
    nsv5285280copy number variation1nstd204human GRCh38.p13 chr20: 44,646,501-44,649,600 , GRCh37.p13 chr20: 43,275,142-43,278,241 ADA
    nsv5282530copy number variation1nstd204human GRCh38.p13 chr20: 44,646,386-44,649,685 , GRCh37.p13 chr20: 43,275,027-43,278,326 ADA
    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
    nsv5022326copy number variation1nstd200human GRCh38 chr20: 32,216,214-44,981,731 , GRCh37.p13 chr20: 30,804,017-43,610,372 , HNF4A, 279 more genes
    nsv5012806copy number variation1nstd200human GRCh38 chr20: 44,649,954-44,653,208 , GRCh37.p13 chr20: 43,278,595-43,281,849 ADA
    nsv5012805copy number variation1nstd200human GRCh38 chr20: 44,646,461-44,649,665 , GRCh37.p13 chr20: 43,275,102-43,278,306 ADA
    nsv5012804copy number variation1nstd200human GRCh38 chr20: 44,640,599-44,640,693 , GRCh37.p13 chr20: 43,269,240-43,269,334 ADA
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