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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5880000copy number variation1nstd209human GRCh38 chr20: 145,382-149,907 , GRCh37.p13 chr20: 126,023-130,548 DEFB126
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5521529copy number variation1nstd206human GRCh38 chr20: 134,335-162,335 , GRCh37.p13 chr20: 114,976-142,976 DEFB126, DEFB127
    nsv5520553copy number variation1nstd206human GRCh38 chr20: 137,830-261,757 , GRCh37.p13 chr20: 118,471-242,398 DEFB126, DEFB127, 3 more genes
    nsv5381806copy number variation1nstd102humanPathogenic GRCh37 chr20: 67,778-974,841 , GRCh38.p12 chr20: 87,137-994,198 DEFB132, LOC101929937, 24 more genes
    nsv5300144copy number variation1nstd204human GRCh38.p13 chr20: 109,225-146,331 , GRCh37.p13 chr20: 89,866-126,972 DEFB126
    nsv5295650copy number variation1nstd204human GRCh38.p13 chr20: 135,801-162,700 , GRCh37.p13 chr20: 116,442-143,341 DEFB127, DEFB126
    nsv5280486copy number variation1nstd204human GRCh38.p13 chr20: 138,841-154,807 , GRCh37.p13 chr20: 119,482-135,448 DEFB126
    nsv4729808copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 61,568-677,437 , GRCh38.p12 chr20: 80,927-696,793 CSNK2A1, SOX12, 18 more genes
    nsv4684288copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-813,880 , GRCh38.p12 chr20: 82,603-833,237 DEFB129, C20orf96, 20 more genes
    nsv4680506copy number variation1nstd189human GRCh37.p13 chr20: 1-627,290 , GRCh38.p12 chr20: 79,361-646,646 , CSNK2A1, 17 more genes
    nsv4676288copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-1,305,971 , GRCh38.p12 chr20: 80,927-1,325,327 TBC1D20, RAD21L1, 34 more genes
    nsv4676270copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-2,269,777 , GRCh38.p12 chr20: 80,927-2,289,131 LOC100289473, STK35, 60 more genes
    nsv4676251copy number variation1nstd102humanUncertain significance GRCh37 chr20: 61,568-121,733 , GRCh38.p12 chr20: 80,927-141,092 DEFB125, DEFB126
    nsv4628131copy number variation2nstd183human GRCh37 chr20: 61,548-189,723 , GRCh38.p12 chr20: 80,907-209,082 DEFB125, DEFB126, 2 more genes
    nsv4627195copy number variation1nstd183human GRCh37 chr20: 64,035-189,655 , GRCh38.p12 chr20: 83,394-209,014 DEFB126, DEFB127, 2 more genes
    nsv4457693copy number variation1nstd102humanUncertain significance GRCh37 chr20: 61,568-491,171 , GRCh38.p12 chr20: 80,927-510,527 C20orf96, DEFB125, 14 more genes
    nsv4420423copy number variation1nstd174human GRCh37 chr20: 61,536-242,395 , GRCh38.p12 chr20: 80,895-261,754 DEFB126, DEFB127, 4 more genes
    nsv4413158copy number variation1nstd174human GRCh37 chr20: 121,783-182,098 , GRCh38.p12 chr20: 141,142-201,457 DEFB126, DEFB127, 1 more genes
    nsv4413154copy number variation1nstd174human GRCh37 chr20: 61,294-139,576 , GRCh38.p12 chr20: 80,653-158,935 DEFB126, DEFB127, 1 more genes
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