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Items: 1 to 20 of 153

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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
    nsv7073834inversion1nstd229human GRCh38 chr20: 39,260,815-44,460,004 , GRCh37.p13 chr20: 37,889,458-43,088,644 LOC100128988, LOC100419859, 72 more genes
    nsv7063922inversion1nstd229human GRCh38 chr20: 43,626,165-43,772,216 , GRCh37.p13 chr20: 42,254,805-42,400,856 RPL27AP, IFT52, 3 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
    nsv7037840copy number variation1nstd229human GRCh38 chr20: 43,703,601-43,772,200 , GRCh37.p13 chr20: 42,332,241-42,400,840 LOC101927200, GTSF1L, 1 more genes
    nsv7021263copy number variation1nstd229human GRCh38 chr20: 43,590,311-43,770,924 , GRCh37.p13 chr20: 42,218,951-42,399,564 GTSF1L, MYBL2, 3 more genes
    nsv6596116inversion1nstd223human GRCh38 chr20: 36,955,253-45,585,469 , GRCh37.p13 chr20: 35,583,656-44,214,108 LOC101929863, LOC105372620, 177 more genes
    nsv6134033copy number variation1nstd213human GRCh37 chr20: 42,170,000-42,740,001 , GRCh38.p12 chr20: 43,541,360-44,111,361 IFT52, JPH2, 11 more genes
    nsv6134007inversion1nstd213human GRCh37 chr20: 42,126,967-42,549,319 , GRCh38.p12 chr20: 43,498,327-43,920,679 MYBL2, SGK2, 10 more genes
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5517831copy number variation1nstd206human GRCh38 chr20: 43,652,961-43,756,992 , GRCh37.p13 chr20: 42,281,601-42,385,632 , RPL27AP, 3 more genes
    nsv5515663copy number variation1nstd206human GRCh38 chr20: 43,718,997-43,731,185 , GRCh37.p13 chr20: 42,347,637-42,359,825 , LOC101927200, 1 more genes
    nsv5324090inversion1nstd204human GRCh37.p13 chr20: 35,583,652-44,214,109 , GRCh38.p13 chr20: 36,955,249-45,585,470 , BPI, 180 more genes
    nsv5033948inversion1nstd200human GRCh38 chr20: 36,955,253-45,585,464 , GRCh37.p13 chr20: 35,583,656-44,214,103 , EMILIN3, 180 more genes
    nsv5028753copy number variation1nstd200human GRCh38 chr20: 43,726,489-43,728,899 , GRCh37.p13 chr20: 42,355,129-42,357,539 , LOC101927200, 1 more genes
    nsv5028752copy number variation1nstd200human GRCh38 chr20: 43,724,591-43,725,533 , GRCh37.p13 chr20: 42,353,231-42,354,173 GTSF1L, LOC101927200
    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
    nsv4884257inversion1nstd200human GRCh37 chr20: 35,583,656-44,214,103 , GRCh38.p12 chr20: 36,955,253-45,585,464 , TGM2, 180 more genes
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