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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137702copy number variation1nstd102humanPathogenic GRCh37 chr9: 35,059,633-37,660,586 , GRCh38.p12 chr9: 35,059,636-37,660,589 ARHGEF39, LOC105376026, 84 more genes
    nsv5717518mobile element insertion1nstd211human GRCh38 chr9: 35,056,093-35,056,093 , GRCh37.p13 chr9: 35,056,090-35,056,090 VCP
    nsv5674074copy number variation1nstd102humanPathogenic GRCh37 chr9: 34,459,004-36,276,941 , GRCh38.p12 chr9: 34,459,006-36,276,944 SPAG8, DNAI1, 84 more genes
    nsv5485633copy number variation1nstd206human GRCh38 chr9: 35,070,421-35,070,490 , GRCh37.p13 chr9: 35,070,418-35,070,487 VCP
    nsv5381707copy number variation2nstd102humanUncertain significance GRCh37 chr9: 34,458,994-35,072,710 , GRCh38.p12 chr9: 34,458,996-35,072,713 YWHAZP6, IL11RA, 30 more genes
    nsv5381688copy number variation1nstd102humanUncertain significance GRCh37 chr9: 35,072,710-35,079,521 , GRCh38.p12 chr9: 35,072,713-35,079,524 FANCG, VCP
    nsv5242427copy number variation1nstd204human GRCh38.p13 chr9: 35,045,752-35,062,807 , GRCh37.p13 chr9: 35,045,749-35,062,804 RN7SL338P, SPATA31G1, 1 more genes
    nsv5194620mobile element insertion1nstd203human GRCh38 chr9: 35,056,080-35,056,093 , GRCh37.p13 chr9: 35,056,077-35,056,090 VCP
    nsv4964296copy number variation1nstd200human GRCh38 chr9: 35,057,600-35,057,751 , GRCh37.p13 chr9: 35,057,597-35,057,748 VCP
    nsv4828257copy number variation1nstd200human GRCh37 chr9: 35,057,597-35,057,748 , GRCh38.p12 chr9: 35,057,600-35,057,751 VCP
    nsv4766654inversion1nstd199human GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552 , ACO1, 876 more genes
    nsv4755256inversion1nstd199human GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552 , ACO1, 876 more genes
    nsv4729230copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 32,192,406-38,311,776 , GRCh38.p12 chr9: 32,192,408-38,311,779 ACO1, ANXA2P2, 210 more genes
    nsv4675565copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-70,984,588 , GRCh38.p12 chr9: 203,861-68,369,672 LOC100132004, LOC105375993, 853 more genes
    nsv4675154copy number variation1nstd102humanUncertain significance GRCh37 chr9: 34,699,039-35,060,746 , GRCh38.p12 chr9: 34,699,042-35,060,749 SYF2P2, YWHAZP6, 13 more genes
    nsv4567227mobile element insertion1nstd166human GRCh37.p13 chr9: 35,056,077-35,056,077 , GRCh38.p12 chr9: 35,056,080-35,056,080 VCP
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4457200copy number variation2nstd102humanPathogenic GRCh37 chr9: 203,861-67,986,965 , GRCh38.p12 chr9: 203,861-67,919,519 ACO1, RNU6-1073P, 846 more genes
    nsv4456028copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-38,472,979 , GRCh38.p12 chr9: 203,861-38,472,982 SNORA30B, LOC100419692, 559 more genes
    nsv4455152copy number variation1nstd102humanPathogenic GRCh37 chr9: 34,542,635-68,210,033 , GRCh38.p12 chr9: 34,542,637-67,920,552 FAM74A6, RGP1, 415 more genes
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