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Items: 1 to 20 of 165

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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
    nsv5705364mobile element insertion1nstd211human GRCh38 chr20: 38,945,409-38,945,409 , GRCh37.p13 chr20: 37,574,052-37,574,052 FAM83D
    nsv5530926copy number variation1nstd206human GRCh38 chr20: 38,918,552-38,972,810 , GRCh37.p13 chr20: 37,547,195-37,601,453 DHX35, FAM83D, 1 more genes
    nsv5513925copy number variation1nstd206human GRCh38 chr20: 38,949,893-39,066,919 , GRCh37.p13 chr20: 37,578,536-37,695,562 NPM1P19, DHX35, 1 more genes
    nsv5366103translocation1nstd200human GRCh38 chr20: 38,945,418-38,945,418 , GRCh38 chr20: 38,944,635-38,944,635 , GRCh37.p13 chr20: 37,574,061-37,574,061 , GRCh37.p13 chr20: 37,573,278-37,573,278 FAM83D
    nsv5366102translocation1nstd200human GRCh38 chr20: 38,944,620-38,944,620 , GRCh38 chr20: 38,945,064-38,945,064 , GRCh37.p13 chr20: 37,573,263-37,573,263 , GRCh37.p13 chr20: 37,573,707-37,573,707 FAM83D
    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
    nsv5028583copy number variation1nstd200human GRCh38 chr20: 38,940,678-38,941,985 , GRCh37.p13 chr20: 37,569,321-37,570,628 FAM83D
    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
    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
    nsv4372070copy number variation1nstd173human GRCh37 chr20: 37,453,865-37,659,416 , GRCh38.p12 chr20: 38,825,222-39,030,773 RN7SL116P, NPM1P19, 3 more genes
    nsv4288474copy number variation1nstd166human GRCh37.p13 chr20: 37,569,331-37,570,628 , GRCh38.p12 chr20: 38,940,688-38,941,985 FAM83D
    nsv4276028copy number variation1nstd166human GRCh37.p13 chr20: 37,552,275-37,553,536 , GRCh38.p12 chr20: 38,923,632-38,924,893 FAM83D
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
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