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Items: 1 to 20 of 145

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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
    nsv7035783copy number variation1nstd229human GRCh38 chr20: 37,446,753-37,638,000 , GRCh37.p13 chr20: 36,075,155-36,266,402 GLRXP1, NNAT, 4 more genes
    nsv7035718copy number variation1nstd229human GRCh38 chr20: 37,519,353-37,527,791 , GRCh37.p13 chr20: 36,147,755-36,156,193 BLCAP, NNAT
    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
    nsv7021547copy number variation1nstd229human GRCh38 chr20: 37,522,358-37,545,892 , GRCh37.p13 chr20: 36,150,760-36,174,294 NNAT, BLCAP, 1 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
    nsv6596116inversion1nstd223human GRCh38 chr20: 36,955,253-45,585,469 , GRCh37.p13 chr20: 35,583,656-44,214,108 LOC101929863, LOC105372620, 177 more genes
    nsv6251419mobile element insertion1nstd215human GRCh38 chr20: 37,522,528-37,522,528 , GRCh37.p13 chr20: 36,150,930-36,150,930 BLCAP, NNAT
    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
    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
    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
    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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