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Items: 1 to 20 of 111

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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
    nsv7097331copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,162,409-44,154,249 , GRCh38.p12 chr6: 42,194,671-44,186,512 MRPS10, CUL9, 70 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
    nsv6794426copy number variation1nstd229human GRCh38 chr6: 43,228,859-43,231,321 , GRCh37.p13 chr6: 43,196,597-43,199,059 DNPH1
    nsv6791704copy number variation1nstd229human GRCh38 chr6: 42,737,001-44,115,000 , GRCh37.p13 chr6: 42,704,739-44,082,737 ZNF318, RPL24P4, 56 more genes
    nsv6788702copy number variation1nstd229human GRCh38 chr6: 42,518,401-43,332,100 , GRCh37.p13 chr6: 42,486,139-43,299,838 DNPH1, MRPL2, 31 more genes
    nsv6787159copy number variation1nstd229human GRCh38 chr6: 43,123,501-43,304,200 , GRCh37.p13 chr6: 43,091,239-43,271,938 PTK7, CRIP3, 5 more genes
    nsv6785753copy number variation1nstd229human GRCh38 chr6: 42,646,801-43,317,300 , GRCh37.p13 chr6: 42,614,539-43,285,038 KLHDC3, CNPY3-GNMT, 30 more genes
    nsv6566770inversion1nstd223human GRCh38 chr6: 42,194,666-44,186,502 , GRCh37.p13 chr6: 42,162,404-44,154,239 RPL36AP5, MIR6780B, 70 more genes
    nsv6414268copy number variation1nstd223human GRCh38 chr6: 43,229,001-43,229,600 , GRCh37.p13 chr6: 43,196,739-43,197,338 DNPH1
    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
    nsv5673766copy number variation1nstd102humanPathogenic GRCh37 chr6: 42,928,506-43,737,486 , GRCh38.p12 chr6: 42,960,768-43,769,749 SRF, POLR1C, 39 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
    nsv5473249copy number variation1nstd206human GRCh38 chr6: 43,226,844-43,227,154 , GRCh37.p13 chr6: 43,194,582-43,194,892 DNPH1
    nsv5461772copy number variation1nstd206human GRCh38 chr6: 43,229,111-43,229,273 , GRCh37.p13 chr6: 43,196,849-43,197,011 DNPH1
    nsv4941138copy number variation1nstd200human GRCh38 chr6: 43,229,111-43,229,273 , GRCh37.p13 chr6: 43,196,849-43,197,011 DNPH1
    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
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