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Items: 1 to 20 of 139

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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
    nsv6796606copy number variation1nstd229human GRCh38 chr6: 42,211,031-42,211,056 , GRCh37.p13 chr6: 42,178,769-42,178,794 MRPS10
    nsv6794084copy number variation1nstd229human GRCh38 chr6: 42,216,015-42,240,182 , GRCh37.p13 chr6: 42,183,753-42,207,920 MRPS10, TRERF1, 1 more genes
    nsv6789272copy number variation1nstd229human GRCh38 chr6: 41,897,601-42,523,500 , GRCh37.p13 chr6: 41,865,339-42,491,238 LOC105375061, RPL36AP5, 13 more genes
    nsv6636814copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,043,510-42,274,148 , GRCh38.p12 chr6: 42,075,772-42,306,410 TRERF1, LOC105375061, 6 more genes
    nsv6570579inversion1nstd223human GRCh38 chr6: 42,209,222-42,209,640 , GRCh37.p13 chr6: 42,176,960-42,177,378 MRPS10
    nsv6566770inversion1nstd223human GRCh38 chr6: 42,194,666-44,186,502 , GRCh37.p13 chr6: 42,162,404-44,154,239 RPL36AP5, MIR6780B, 70 more genes
    nsv6565530inversion1nstd223human GRCh38 chr6: 42,215,203-42,215,683 , GRCh37.p13 chr6: 42,182,941-42,183,421 MRPS10
    nsv6562399inversion1nstd223human GRCh38 chr6: 42,209,037-42,209,763 , GRCh37.p13 chr6: 42,176,775-42,177,501 MRPS10
    nsv6410144copy number variation1nstd223human GRCh38 chr6: 42,209,604-42,213,246 , GRCh37.p13 chr6: 42,177,342-42,180,984 MRPS10
    nsv6407351copy number variation1nstd223human GRCh38 chr6: 42,209,197-42,219,811 , GRCh37.p13 chr6: 42,176,935-42,187,549 MRPS10
    nsv6137126translocation1nstd213human GRCh38.p12 chr16: 72,075,817-72,075,817 , GRCh37 chr16: 72,109,716-72,109,716 , GRCh38.p12 chr6: 42,207,729-42,207,729 , GRCh37 chr6: 42,175,467-42,175,467 HPR, TXNL4B, 1 more genes
    nsv6136877translocation1nstd213human GRCh38.p12 chr16: 72,075,815-72,075,815 , GRCh37 chr16: 72,109,714-72,109,714 , GRCh38.p12 chr6: 42,207,801-42,207,801 , GRCh37 chr6: 42,175,539-42,175,539 HPR, TXNL4B, 1 more genes
    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
    nsv5963626insertion1nstd209human GRCh38 chr6: 42,216,385-42,216,385 , GRCh37.p13 chr6: 42,184,123-42,184,123 MRPS10
    nsv5640593insertion1nstd207human GRCh38 chr6: 42,216,385-42,216,385 , GRCh37.p13 chr6: 42,184,123-42,184,123 MRPS10
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
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