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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097826copy number variation1nstd102humanPathogenic GRCh37 chr6: 41,126,341-43,752,536 , GRCh38.p12 chr6: 41,158,603-43,784,799 USP49, PRICKLE4, 96 more genes
    nsv7097825copy number variation1nstd102humanUncertain significance GRCh37 chr6: 41,126,341-43,737,486 , GRCh38.p12 chr6: 41,158,603-43,769,749 DNPH1, LOC107986596, 96 more genes
    nsv7043293inversion1nstd229human GRCh38 chr6: 39,854,165-43,261,822 , GRCh37.p13 chr6: 39,821,941-43,229,560 RPL23P6, RPL32P15, 95 more genes
    nsv7039251inversion1nstd229human GRCh38 chr6: 41,293,900-41,424,940 , GRCh37.p13 chr6: 41,261,638-41,392,678 NCR2, RPL32P15, 2 more genes
    nsv6782486copy number variation1nstd229human GRCh38 chr6: 41,282,267-41,453,688 , GRCh37.p13 chr6: 41,250,005-41,421,426 TREM1, LOC112267957, 5 more genes
    nsv6782400copy number variation1nstd229human GRCh38 chr6: 41,378,649-41,401,052 , GRCh37.p13 chr6: 41,346,387-41,368,790 LOC100505711
    nsv6779435copy number variation1nstd229human GRCh38 chr6: 41,376,690-41,386,238 , GRCh37.p13 chr6: 41,344,428-41,353,976 LOC100505711
    nsv6779197copy number variation1nstd229human GRCh38 chr6: 41,311,001-41,424,900 , GRCh37.p13 chr6: 41,278,739-41,392,638 NCR2, LOC100505711
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv5955029insertion1nstd209human GRCh38 chr6: 41,381,418-41,381,418 , GRCh37.p13 chr6: 41,349,156-41,349,156 LOC100505711
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5465830copy number variation1nstd206human GRCh38 chr6: 41,337,530-41,423,369 , GRCh37.p13 chr6: 41,305,268-41,391,107 NCR2, LOC100505711
    nsv4941068copy number variation1nstd200human GRCh38 chr6: 41,376,690-41,386,235 , GRCh37.p13 chr6: 41,344,428-41,353,973 LOC100505711
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv4133087copy number variation1nstd166human GRCh37.p13 chr6: 41,344,428-41,353,973 , GRCh38.p12 chr6: 41,376,690-41,386,235 LOC100505711
    nsv3919521copy number variation1nstd102humanPathogenic NCBI36 chr6: 37,853,123-45,729,558 , GRCh37 chr6: 37,745,145-45,621,580 , GRCh38 chr6: 37,777,369-45,653,843 RPL23P6, LOC102723789, 184 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
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