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Items: 1 to 20 of 116

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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
    nsv7053006inversion1nstd229human GRCh38 chr6: 41,251,993-41,310,987 , GRCh37.p13 chr6: 41,219,731-41,278,725 RPL32P15, RNU6-643P, 1 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
    nsv6792223copy number variation1nstd229human GRCh38 chr6: 41,283,781-41,290,119 , GRCh37.p13 chr6: 41,251,519-41,257,857 TREM1
    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
    nsv6780035copy number variation1nstd229human GRCh38 chr6: 41,267,256-41,270,998 , GRCh37.p13 chr6: 41,234,994-41,238,736 TREM1
    nsv6778719copy number variation1nstd229human GRCh38 chr6: 41,257,053-41,267,836 , GRCh37.p13 chr6: 41,224,791-41,235,574 TREM1
    nsv6563758inversion1nstd223human GRCh38 chr6: 41,277,965-41,278,392 , GRCh37.p13 chr6: 41,245,703-41,246,130 TREM1
    nsv6404029copy number variation1nstd223human GRCh38 chr6: 41,267,256-41,270,995 , GRCh37.p13 chr6: 41,234,994-41,238,733 TREM1
    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
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5467669copy number variation1nstd206human GRCh38 chr6: 41,283,781-41,290,119 , GRCh37.p13 chr6: 41,251,519-41,257,857 TREM1
    nsv5109638mobile element insertion1nstd203human GRCh38 chr6: 41,266,884-41,266,892 , GRCh37.p13 chr6: 41,234,622-41,234,630 TREM1
    nsv4941065copy number variation1nstd200human GRCh38 chr6: 41,283,781-41,290,119 , GRCh37.p13 chr6: 41,251,519-41,257,857 TREM1
    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
    nsv4675176copy number variation1nstd102humanUncertain significance GRCh37 chr6: 41,200,840-41,331,797 , GRCh38.p12 chr6: 41,233,102-41,364,059 NCR2, RPL32P15, 5 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
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