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Items: 1 to 20 of 133

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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
    nsv7070202inversion1nstd229human GRCh38 chr10: 27,330,033-30,802,827 , GRCh37.p13 chr10: 27,618,962-31,091,756 LINC00837, RPL21P93, 77 more genes
    nsv7058187inversion1nstd229human GRCh38 chr10: 27,002,297-30,809,591 , GRCh37.p13 chr10: 27,291,226-31,098,520 RNU6-490P, LOC105376474, 87 more genes
    nsv6894377copy number variation1nstd229human GRCh38 chr10: 28,466,728-36,061,502 , GRCh37.p13 chr10: 28,755,657-36,350,430 LOC105376482, LOC101929431, 130 more genes
    nsv6882555copy number variation1nstd229human GRCh38 chr10: 28,624,852-29,199,161 , GRCh37.p13 chr10: 28,913,781-29,488,090 RNU4ATAC6P, LOC107984171, 12 more genes
    nsv6582027inversion1nstd223human GRCh38 chr10: 26,903,422-36,846,484 , GRCh37.p13 chr10: 27,192,351-37,135,412 KIF5B, EPC1-AS1, 167 more genes
    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
    nsv6291211copy number variation1nstd102humanPathogenic GRCh37 chr10: 27,204,530-29,105,882 , GRCh38.p12 chr10: 26,915,601-28,816,953 LINC02673, FAM210CP, 44 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6240521mobile element insertion1nstd215human GRCh38 chr10: 28,788,276-28,788,276 , GRCh37.p13 chr10: 29,077,205-29,077,205 LINC01517, LINC00837
    nsv6131782copy number variation1nstd213human GRCh37 chr10: 28,950,000-33,420,001 , GRCh38.p12 chr10: 28,661,071-33,131,073 CCND3P1, MAP3K8, 88 more genes
    nsv6083200insertion1nstd212human GRCh38 chr10: 28,788,265-28,788,265 , GRCh37.p13 chr10: 29,077,194-29,077,194 LINC01517, LINC00837
    nsv5966263insertion1nstd209human GRCh38 chr10: 28,788,263-28,788,263 , GRCh37.p13 chr10: 29,077,192-29,077,192 LINC00837, LINC01517
    nsv5914382copy number variation1nstd209human GRCh38 chr10: 27,312,316-36,846,398 , GRCh37.p13 chr10: 27,601,245-37,135,326 , RN7SL241P, 160 more genes
    nsv5703311mobile element insertion2nstd211human GRCh38 chr10: 28,788,276-28,788,276 , GRCh37.p13 chr10: 29,077,205-29,077,205 LINC01517, LINC00837
    nsv5643134insertion1nstd207human GRCh38 chr10: 28,788,263-28,788,263 , GRCh37.p13 chr10: 29,077,192-29,077,192 LINC01517, LINC00837
    nsv5137199mobile element insertion1nstd203human GRCh38 chr10: 28,788,268-28,788,276 , GRCh37.p13 chr10: 29,077,197-29,077,205 LINC01517, LINC00837
    nsv5131801mobile element insertion1nstd203human GRCh38 chr10: 28,788,267-28,788,276 , GRCh37.p13 chr10: 29,077,196-29,077,205 LINC00837, LINC01517
    nsv5130662mobile element insertion1nstd203human GRCh38 chr10: 28,788,265-28,788,276 , GRCh37.p13 chr10: 29,077,194-29,077,205 LINC01517, LINC00837
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