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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096025copy number variation1nstd102humanUncertain significance GRCh37 chr20: 35,569,422-36,500,415 , GRCh38.p12 chr20: 36,941,019-37,872,013 RPN2, SAMHD1, 19 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
    nsv7034498copy number variation1nstd229human GRCh38 chr20: 37,143,392-40,581,574 , GRCh37.p13 chr20: 35,771,795-39,210,214 ADIG, TGM2, 61 more genes
    nsv7021198copy number variation1nstd229human GRCh38 chr20: 33,145,032-41,995,765 , GRCh37.p13 chr20: 31,732,838-40,624,405 PXMP4, RPL12P11, 199 more genes
    nsv6596584inversion1nstd223human GRCh38 chr20: 37,683,235-37,683,606 , GRCh37.p13 chr20: 36,311,637-36,312,008 LOC100287792
    nsv6596116inversion1nstd223human GRCh38 chr20: 36,955,253-45,585,469 , GRCh37.p13 chr20: 35,583,656-44,214,108 LOC101929863, LOC105372620, 177 more genes
    nsv6134289copy number variation1nstd213human GRCh37 chr20: 35,530,000-37,610,001 , GRCh38.p12 chr20: 36,901,597-38,981,358 GHRH, RBL1, 51 more genes
    nsv6133915copy number variation1nstd213human GRCh37 chr20: 36,310,000-37,530,001 , GRCh38.p12 chr20: 37,681,598-38,901,358 BPI, LBP, 30 more genes
    nsv6133809copy number variation1nstd213human GRCh37 chr20: 36,080,000-36,310,001 , GRCh38.p12 chr20: 37,451,598-37,681,599 NNAT, BLCAP, 5 more genes
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5963085copy number variation1nstd209human GRCh38 chr20: 37,683,604-37,683,899 , GRCh37.p13 chr20: 36,312,006-36,312,301 LOC100287792
    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
    nsv5028545copy number variation1nstd200human GRCh38 chr20: 37,681,162-37,683,109 , GRCh37.p13 chr20: 36,309,564-36,311,511 LOC100287792
    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
    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
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