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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138180insertion1nstd232human GRCh37.p13 chr10: 15,879,317-15,879,317 , GRCh38.p12 chr10: 15,837,318-15,837,318 MINDY3
    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
    nsv7071213inversion1nstd229human GRCh38 chr10: 15,424,724-15,994,382 , GRCh37.p13 chr10: 15,466,723-16,036,381 ITGA8, MINDY3
    nsv7060184inversion1nstd229human GRCh38 chr10: 13,148,010-16,128,795 , GRCh37.p13 chr10: 13,190,010-16,170,794 LOC101928453, MCM10, 52 more genes
    nsv6897178copy number variation1nstd229human GRCh38 chr10: 15,835,704-15,874,005 , GRCh37.p13 chr10: 15,877,703-15,916,004 MINDY3
    nsv6897049copy number variation1nstd229human GRCh38 chr10: 15,845,099-15,845,190 , GRCh37.p13 chr10: 15,887,098-15,887,189 MINDY3
    nsv6895624copy number variation1nstd229human GRCh38 chr10: 15,804,820-15,808,792 , GRCh37.p13 chr10: 15,846,819-15,850,791 MINDY3
    nsv6895206copy number variation1nstd229human GRCh38 chr10: 15,629,216-15,981,555 , GRCh37.p13 chr10: 15,671,215-16,023,554 MINDY3, ITGA8
    nsv6892478copy number variation1nstd229human GRCh38 chr10: 15,858,231-15,859,244 , GRCh37.p13 chr10: 15,900,230-15,901,243 MINDY3
    nsv6889616copy number variation1nstd229human GRCh38 chr10: 15,710,942-15,776,564 , GRCh37.p13 chr10: 15,752,941-15,818,563 MINDY3, ITGA8
    nsv6888014copy number variation1nstd229human GRCh38 chr10: 15,789,021-15,789,151 , GRCh37.p13 chr10: 15,831,020-15,831,150 MINDY3
    nsv6886350copy number variation1nstd229human GRCh38 chr10: 15,836,744-15,837,046 , GRCh37.p13 chr10: 15,878,743-15,879,045 MINDY3
    nsv6884320copy number variation1nstd229human GRCh38 chr10: 15,770,801-15,841,500 , GRCh37.p13 chr10: 15,812,800-15,883,499 MINDY3
    nsv6883666copy number variation1nstd229human GRCh38 chr10: 15,806,189-15,815,580 , GRCh37.p13 chr10: 15,848,188-15,857,579 MINDY3
    nsv6881841copy number variation1nstd229human GRCh38 chr10: 15,834,615-15,836,927 , GRCh37.p13 chr10: 15,876,614-15,878,926 MINDY3
    nsv6881353copy number variation1nstd229human GRCh38 chr10: 15,783,693-15,785,907 , GRCh37.p13 chr10: 15,825,692-15,827,906 MINDY3
    nsv6879698copy number variation1nstd229human GRCh38 chr10: 15,676,635-16,644,236 , GRCh37.p13 chr10: 15,718,634-16,686,235 FTLP19, LINC02654, 7 more genes
    nsv6593886inversion1nstd223human GRCh38 chr10: 15,811,975-15,816,252 , GRCh37.p13 chr10: 15,853,974-15,858,251 MINDY3
    nsv6581480inversion1nstd223human GRCh38 chr10: 15,804,410-15,805,264 , GRCh37.p13 chr10: 15,846,409-15,847,263 MINDY3
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