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Items: 1 to 20 of 166

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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
    nsv6137700copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,088,563-39,092,820 , GRCh38.p12 chr9: 36,088,566-39,092,823 SNX18P3, VN1R48P, 69 more genes
    nsv5972210inversion1nstd209human GRCh38 chr9: 36,238,245-37,822,315 , GRCh37.p13 chr9: 36,238,242-37,822,312 PAX5, GRHPR, 35 more genes
    nsv5713345mobile element insertion1nstd211human GRCh38 chr9: 36,302,886-36,302,886 , GRCh37.p13 chr9: 36,302,883-36,302,883 LOC102724322, HMGB3P24
    nsv5486993copy number variation1nstd206human GRCh38 chr9: 36,300,270-36,301,238 , GRCh37.p13 chr9: 36,300,267-36,301,235 HMGB3P24, LOC102724322
    nsv4964344copy number variation1nstd200human GRCh38 chr9: 36,304,307-36,307,657 , GRCh37.p13 chr9: 36,304,304-36,307,654 LOC102724322, HMGB3P24
    nsv4964343copy number variation1nstd200human GRCh38 chr9: 36,301,260-36,305,250 , GRCh37.p13 chr9: 36,301,257-36,305,247 LOC102724322, HMGB3P24
    nsv4964342copy number variation1nstd200human GRCh38 chr9: 36,301,635-36,301,713 , GRCh37.p13 chr9: 36,301,632-36,301,710 LOC102724322, HMGB3P24
    nsv4964341copy number variation1nstd200human GRCh38 chr9: 36,300,270-36,301,238 , GRCh37.p13 chr9: 36,300,267-36,301,235 LOC102724322, HMGB3P24
    nsv4828286copy number variation1nstd200human GRCh37 chr9: 36,301,632-36,301,710 , GRCh38.p12 chr9: 36,301,635-36,301,713 LOC102724322, HMGB3P24
    nsv4828285copy number variation1nstd200human GRCh37 chr9: 36,301,275-36,305,246 , GRCh38.p12 chr9: 36,301,278-36,305,249 LOC102724322, HMGB3P24
    nsv4828284copy number variation1nstd200human GRCh37 chr9: 36,300,267-36,301,235 , GRCh38.p12 chr9: 36,300,270-36,301,238 LOC102724322, HMGB3P24
    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
    nsv4614948copy number variation1nstd183human GRCh37 chr9: 36,073,433-36,548,242 , GRCh38.p12 chr9: 36,073,436-36,548,245 RNU4-53P, RECK, 8 more genes
    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
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