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Items: 1 to 20 of 267

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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
    nsv5955830copy number variation1nstd209human GRCh38 chr20: 37,361,798-37,361,869 , GRCh37.p13 chr20: 35,990,201-35,990,272 SRC
    nsv5877152copy number variation1nstd209human GRCh38 chr20: 37,367,236-37,369,441 , GRCh37.p13 chr20: 35,995,639-35,997,844 SRC
    nsv5714250mobile element insertion1nstd211human GRCh38 chr20: 37,379,967-37,379,967 , GRCh37.p13 chr20: 36,008,370-36,008,370 SRC
    nsv5665933insertion1nstd207human GRCh38 chr20: 37,361,870-37,361,870 , GRCh37.p13 chr20: 35,990,273-35,990,273 SRC
    nsv5592628copy number variation1nstd207human GRCh38 chr20: 37,361,798-37,361,869 , GRCh37.p13 chr20: 35,990,201-35,990,272 SRC
    nsv5592563copy number variation1nstd207human GRCh38 chr20: 37,379,895-37,379,950 , GRCh37.p13 chr20: 36,008,298-36,008,353 SRC
    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
    nsv5028529copy number variation1nstd200human GRCh38 chr20: 37,359,716-37,360,002 , GRCh37.p13 chr20: 35,988,119-35,988,405 SRC
    nsv5025570copy number variation1nstd200human GRCh38 chr20: 37,347,043-37,347,744 , GRCh37.p13 chr20: 35,975,446-35,976,147 SRC
    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
    nsv4732391copy number variation1nstd199human GRCh37 chr20: 35,990,213-35,990,285 , GRCh38.p12 chr20: 37,361,810-37,361,882 SRC
    nsv4674805copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 34,980,430-46,806,549 , GRCh38.p12 chr20: 36,352,027-48,177,806 ADA, BPI, 266 more genes
    nsv4440823copy number variation1nstd175human GRCh37 chr20: 35,990,201-35,990,273 , GRCh38.p12 chr20: 37,361,798-37,361,870 SRC
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