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Items: 1 to 20 of 198

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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
    nsv5714103mobile element insertion1nstd211human GRCh38 chr20: 43,542,597-43,542,597 , GRCh37.p13 chr20: 42,171,237-42,171,237 L3MBTL1
    nsv5366120translocation1nstd200human GRCh38 chr20: 43,538,612-43,538,612 , GRCh38 chrX: 11,713,890-11,713,890 , GRCh37.p13 chr20: 42,167,252-42,167,252 , GRCh37.p13 chrX: 11,732,010-11,732,010 L3MBTL1
    nsv5324090inversion1nstd204human GRCh37.p13 chr20: 35,583,652-44,214,109 , GRCh38.p13 chr20: 36,955,249-45,585,470 , BPI, 180 more genes
    nsv5160327mobile element insertion1nstd203human GRCh38 chr20: 43,518,865-43,518,865 , GRCh37.p13 chr20: 42,147,505-42,147,505 L3MBTL1
    nsv5033948inversion1nstd200human GRCh38 chr20: 36,955,253-45,585,464 , GRCh37.p13 chr20: 35,583,656-44,214,103 , EMILIN3, 180 more genes
    nsv5028737copy number variation1nstd200human GRCh38 chr20: 43,523,094-43,523,267 , GRCh37.p13 chr20: 42,151,734-42,151,907 LOC107985380, L3MBTL1
    nsv5028736copy number variation1nstd200human GRCh38 chr20: 43,508,829-43,512,331 , GRCh37.p13 chr20: 42,137,469-42,140,971 L3MBTL1
    nsv5025623copy number variation1nstd200human GRCh38 chr20: 43,550,807-43,556,268 , GRCh37.p13 chr20: 42,179,447-42,184,908 L3MBTL1
    nsv5025622copy number variation1nstd200human GRCh38 chr20: 43,505,107-43,509,306 , GRCh37.p13 chr20: 42,133,747-42,137,946 L3MBTL1
    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
    nsv4865577copy number variation1nstd200human GRCh37 chr20: 42,133,747-42,137,946 , GRCh38.p12 chr20: 43,505,107-43,509,306 L3MBTL1
    nsv4853619copy number variation1nstd200human GRCh37 chr20: 42,151,734-42,151,907 , GRCh38.p12 chr20: 43,523,094-43,523,267 L3MBTL1, LOC107985380
    nsv4853618copy number variation1nstd200human GRCh37 chr20: 42,137,469-42,140,971 , GRCh38.p12 chr20: 43,508,829-43,512,331 L3MBTL1
    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
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