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Items: 1 to 20 of 236

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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
    nsv5667115insertion1nstd207human GRCh38 chr20: 37,914,404-37,914,404 , GRCh37.p13 chr20: 36,542,806-36,542,806 VSTM2L
    nsv5324090inversion1nstd204human GRCh37.p13 chr20: 35,583,652-44,214,109 , GRCh38.p13 chr20: 36,955,249-45,585,470 , BPI, 180 more genes
    nsv5169427mobile element insertion1nstd203human GRCh38 chr20: 37,937,556-37,937,571 , GRCh37.p13 chr20: 36,565,958-36,565,973 VSTM2L
    nsv5033948inversion1nstd200human GRCh38 chr20: 36,955,253-45,585,464 , GRCh37.p13 chr20: 35,583,656-44,214,103 , EMILIN3, 180 more genes
    nsv5028549copy number variation1nstd200human GRCh38 chr20: 37,937,972-37,942,703 , GRCh37.p13 chr20: 36,566,374-36,571,105 VSTM2L
    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
    nsv4868789copy number variation1nstd200human GRCh37 chr20: 36,566,374-36,571,105 , GRCh38.p12 chr20: 37,937,972-37,942,703 VSTM2L
    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
    nsv4755109insertion1nstd199human GRCh37 chr20: 36,542,796-36,542,796 , GRCh38.p12 chr20: 37,914,394-37,914,394 VSTM2L
    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
    nsv4512040mobile element insertion1nstd166human GRCh37.p13 chr20: 36,550,240-36,550,240 , GRCh38.p12 chr20: 37,921,838-37,921,838 VSTM2L
    nsv4443863insertion1nstd175human GRCh37 chr20: 36,542,806-36,542,806 , GRCh38.p12 chr20: 37,914,404-37,914,404 VSTM2L
    nsv4339997sequence alteration1nstd166human GRCh37.p13 chr20: 36,540,780-36,548,420 , GRCh38.p12 chr20: 37,912,378-37,920,018 VSTM2L
    nsv4285575copy number variation1nstd166human GRCh37.p13 chr20: 36,542,841-36,542,911 , GRCh38.p12 chr20: 37,914,439-37,914,509 VSTM2L
    nsv4277375copy number variation1nstd166human GRCh37.p13 chr20: 36,531,054-36,531,108 , GRCh38.p12 chr20: 37,902,652-37,902,706 VSTM2L
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