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Items: 1 to 20 of 266

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112722copy number variation1nstd102humanPathogenic GRCh37 chrX: 42,069,104-45,843,277 , GRCh38.p12 chrX: 42,209,851-45,983,842 TATDN2P1, RRM2P3, 36 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
    nsv5873682copy number variation1nstd209human GRCh38 chrX: 41,560,623-47,265,899 , GRCh37.p13 chrX: 41,419,876-47,125,298 , CTNNBL1P1, 80 more genes
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5381749copy number variation1nstd102humanPathogenic GRCh37 chrX: 39,645,568-44,199,000 , GRCh38.p12 chrX: 39,786,314-44,339,754 EFHC2, GPR82, 58 more genes
    nsv5381697copy number variation1nstd102humanPathogenic GRCh37 chrX: 41,342,834-43,901,936 , GRCh38.p12 chrX: 41,483,581-44,042,690 GPR82, RNU6-1124P, 22 more genes
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4905429copy number variation1nstd200human GRCh38 chrX: 42,865,602-43,069,445 , GRCh37.p13 chrX: 42,724,851-42,928,694 , LOC105373188, 1 more genes
    nsv4781968copy number variation1nstd200human GRCh37 chrX: 42,724,851-42,928,694 , GRCh38.p12 chrX: 42,865,602-43,069,445 , LOC105373188, 1 more genes
    nsv4728486copy number variation1nstd102humanPathogenic GRCh37 chrX: 219,609-55,466,476 , GRCh38.p12 chrX: 302,942-55,440,043 CDK16, WASF4P, 772 more genes
    nsv4685953copy number variation1nstd102humanPathogenic GRCh37 chrX: 41,150,139-43,976,458 , GRCh38.p12 chrX: 41,290,886-44,117,212 GEMIN7P1, PINCR, 28 more genes
    nsv4684016inversion1nstd191human GRCh37.p13 chrX: 32,933,886-87,244,324 , GRCh38 chrX: 32,915,769-87,989,324 , ABCB7, 816 more genes
    nsv4674588copy number variation1nstd102humanPathogenic GRCh37 chrX: 539,722-55,509,385 , GRCh38.p12 chrX: 578,987-55,482,952 LOC392440, SSX4, 769 more genes
    nsv4674581copy number variation1nstd102humanPathogenic GRCh37 chrX: 32,849,282-43,713,387 , GRCh38.p12 chrX: 32,831,165-43,854,141 BCOR, RN7SL732P, 116 more genes
    nsv4674013copy number variation1nstd102humanUncertain significance GRCh37 chrX: 42,632,238-42,988,722 , GRCh38.p12 chrX: 42,772,987-43,129,473 PPP1R2C, LOC105373188, 1 more genes
    nsv4578278inversion1nstd102humanLikely pathogenic GRCh37 chrX: 32,196,272-75,245,806 , GRCh38.p12 chrX: 32,178,155-76,025,971 ABCB7, ACTG1P10, 704 more genes
    nsv4452472copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-61,877,279 , GRCh38.p12 chrX: 251,879-62,657,809 MIR660, RNU6-1321P, 802 more genes
    nsv4451112copy number variation1nstd102humanPathogenic GRCh37 chrX: 42,165,435-43,684,005 , GRCh38.p12 chrX: 42,306,183-43,824,758 PINCR, NANOGP10, 8 more genes
    nsv4450820copy number variation1nstd102humanPathogenic GRCh37 chrX: 40,572,613-92,796,528 , GRCh38.p12 chrX: 40,713,361-93,541,529 HNRNPA1P25, MPV17L2P1, 755 more genes
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