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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137736copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,263,517-155,260,560 , GRCh38.p12 chrX: 153,998,066-156,030,895 H2AB3, GDI1, 83 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5979027copy number variation2nstd209human GRCh38 chrX: 155,924,633-155,931,613 , GRCh37.p13 chrX: 155,154,297-155,161,277 VAMP7
    nsv5978701copy number variation2nstd209human GRCh38 chrX: 155,889,512-155,904,807 , GRCh37.p13 chrX: 155,119,175-155,134,471 VAMP7
    nsv5978235copy number variation2nstd209human GRCh38 chrX: 155,916,433-155,921,432 , GRCh37.p13 chrX: 155,146,097-155,151,096 VAMP7
    nsv5976142inversion1nstd209human GRCh38 chrX: 155,890,514-155,931,331 , GRCh37.p13 chrX: 155,120,177-155,160,995 VAMP7
    nsv5975658copy number variation2nstd209human GRCh38 chrX: 155,879,937-155,895,014 , GRCh37.p13 chrX: 155,109,600-155,124,677 VAMP7
    nsv5972699copy number variation2nstd209human GRCh38 chrX: 155,903,924-155,924,082 , GRCh37.p13 chrX: 155,133,588-155,153,746 VAMP7
    nsv5971454copy number variation2nstd209human GRCh38 chrX: 155,873,487-155,883,386 , GRCh37.p13 chrX: 155,103,150-155,113,049 DPH3P2, VAMP7
    nsv5969356copy number variation2nstd209human GRCh38 chrX: 155,907,119-155,911,486 , GRCh37.p13 chrX: 155,136,783-155,141,150 VAMP7
    nsv5969254copy number variation2nstd209human GRCh38 chrX: 155,943,234-155,950,533 , GRCh37.p13 chrX: 155,172,898-155,180,198 VAMP7
    nsv5969220copy number variation2nstd209human GRCh38 chrX: 155,925,933-155,943,633 , GRCh37.p13 chrX: 155,155,597-155,173,297 VAMP7
    nsv5875385copy number variation1nstd209human GRCh38 chrX: 155,641,885-155,958,610 , GRCh37.p13 chrX: 154,906,586-155,188,275 AMD1P2, VAMP7, 2 more genes
    nsv5871411copy number variation1nstd209human GRCh38 chrX: 155,803,598-155,984,221 , GRCh37.p13 chrX: 155,033,261-155,213,886 AMD1P2, VAMP7, 3 more genes
    nsv5722442mobile element insertion2nstd211human GRCh38 chrX: 155,900,594-155,900,594 , GRCh37.p13 chrX: 155,130,258-155,130,258 VAMP7
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5665408inversion1nstd207human GRCh37.p13 chrX: 154,937,871-155,260,559 , GRCh38 chrX: 155,708,210-156,030,894 AMD1P2, IL9R, 8 more genes
    nsv5424596copy number variation1nstd206human GRCh38 chrX: 155,902,021-156,003,787 , GRCh37.p13 chrX: 155,131,685-155,233,452 ELOCP24, IL9R, 2 more genes
    nsv5424054copy number variation1nstd206human GRCh38 chrX: 155,891,000-155,903,000 , GRCh37.p13 chrX: 155,120,663-155,132,664 VAMP7
    nsv5422912copy number variation1nstd206human GRCh38 chrX: 155,892,881-155,893,014 , GRCh37.p13 chrX: 155,122,544-155,122,677 VAMP7
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