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Items: 1 to 20 of 226

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7073282inversion1nstd229human GRCh38 chr10: 12,099,288-14,830,781 , GRCh37.p13 chr10: 12,141,287-14,872,780 MIR1265, RNA5SP301, 45 more genes
    nsv7072872inversion1nstd229human GRCh38 chr10: 13,148,957-13,172,261 , GRCh37.p13 chr10: 13,190,957-13,214,261 MCM10, BTBD7P1, 1 more genes
    nsv7061969inversion1nstd229human GRCh38 chr10: 11,128,019-14,526,691 , GRCh37.p13 chr10: 11,169,982-14,568,690 RPL5P25, LOC105376425, 58 more genes
    nsv7060184inversion1nstd229human GRCh38 chr10: 13,148,010-16,128,795 , GRCh37.p13 chr10: 13,190,010-16,170,794 LOC101928453, MCM10, 52 more genes
    nsv7058695inversion1nstd229human GRCh38 chr10: 11,787,108-13,297,144 , GRCh37.p13 chr10: 11,829,107-13,339,144 RNU6-6P, SEC61A2, 28 more genes
    nsv6896541copy number variation1nstd229human GRCh38 chr10: 13,210,947-13,223,143 , GRCh37.p13 chr10: 13,252,947-13,265,143 UCMA, RNU6-6P, 1 more genes
    nsv6891548copy number variation1nstd229human GRCh38 chr10: 13,208,500-13,222,996 , GRCh37.p13 chr10: 13,250,500-13,264,996 RNU6-6P, MCM10, 1 more genes
    nsv6881363copy number variation1nstd229human GRCh38 chr10: 13,148,752-13,202,272 , GRCh37.p13 chr10: 13,190,752-13,244,272 MCM10, RPL36AP36, 1 more genes
    nsv6880605copy number variation1nstd229human GRCh38 chr10: 13,146,265-13,168,592 , GRCh37.p13 chr10: 13,188,265-13,210,592 RPL36AP36, MCM10, 1 more genes
    nsv6878281copy number variation1nstd229human GRCh38 chr10: 13,135,792-13,170,011 , GRCh37.p13 chr10: 13,177,792-13,212,011 OPTN, MCM10, 2 more genes
    nsv6592458inversion1nstd223human GRCh38 chr10: 11,934,638-13,951,892 , GRCh37.p13 chr10: 11,976,637-13,993,892 RNU6-6P, MIR548Q, 38 more genes
    nsv6580776inversion1nstd223human GRCh38 chr10: 13,174,212-13,174,993 , GRCh37.p13 chr10: 13,216,212-13,216,993 MCM10
    nsv6575851inversion1nstd223human GRCh38 chr10: 13,194,244-13,195,629 , GRCh37.p13 chr10: 13,236,244-13,237,629 MCM10
    nsv6452681copy number variation1nstd223human GRCh38 chr10: 13,210,947-13,223,140 , GRCh37.p13 chr10: 13,252,947-13,265,140 RNU6-6P, UCMA, 1 more genes
    nsv6445168copy number variation1nstd223human GRCh38 chr10: 13,133,227-13,198,574 , GRCh37.p13 chr10: 13,175,227-13,240,574 OPTN, RPL36AP36, 2 more genes
    nsv6436482copy number variation1nstd223human GRCh38 chr10: 13,165,606-13,166,514 , GRCh37.p13 chr10: 13,207,606-13,208,514 MCM10
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 more genes
    nsv6308978copy number variation1nstd102humanUncertain significance GRCh37 chr10: 12,111,033-13,342,042 , GRCh38.p12 chr10: 12,069,034-13,300,042 LOC105376418, CDC123, 23 more genes
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