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Items: 1 to 20 of 282

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5873004copy number variation1nstd209human GRCh38 chrX: 37,651,918-42,011,744 , GRCh37.p13 chrX: 37,669,767-41,870,997 , USP9X, 72 more genes
    nsv5674145copy number variation1nstd102humanPathogenic GRCh37 chrX: 37,545,215-38,280,335 , GRCh38.p12 chrX: 37,685,962-38,421,082 DYNLT3, H2AL3, 11 more genes
    nsv5564461copy number variation1nstd102humanUncertain significance GRCh37 chrX: 37,545,209-38,186,626 , GRCh38.p12 chrX: 37,685,956-38,327,373 H2AP, DYNLT3, 9 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
    nsv4905393copy number variation1nstd200human GRCh38 chrX: 37,928,888-38,150,186 , GRCh37.p13 chrX: 37,788,141-38,009,439 SC4MOP, SRPX, 4 more genes
    nsv4905391copy number variation1nstd200human GRCh38 chrX: 37,655,592-38,492,757 , GRCh37.p13 chrX: 37,669,767-38,352,010 SRPX, CYBB, 14 more genes
    nsv4781944copy number variation1nstd200human GRCh37 chrX: 37,788,141-38,009,439 , GRCh38.p12 chrX: 37,928,888-38,150,186 H2AP, H2AL3, 4 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
    nsv4728331copy number variation1nstd102humanUncertain significance GRCh37 chrX: 37,487,291-38,568,933 , GRCh38.p12 chrX: 37,628,038-38,709,679 XK, SYTL5, 17 more genes
    nsv4685868copy number variation1nstd102humanPathogenic GRCh37 chrX: 35,820,200-38,547,007 , GRCh38.p12 chrX: 35,802,083-38,687,753 MIR548AJ2, CFAP47, 36 more genes
    nsv4684016inversion1nstd191human GRCh37.p13 chrX: 32,933,886-87,244,324 , GRCh38 chrX: 32,915,769-87,989,324 , ABCB7, 816 more genes
    nsv4683403copy number variation1nstd102humanPathogenic GRCh37 chrX: 37,639,262-38,280,355 , GRCh38.p12 chrX: 37,780,009-38,421,102 RNU6-49P, CRIPTOP1, 10 more genes
    nsv4682173copy number variation1nstd102humanPathogenic GRCh37 chrX: 30,326,313-41,000,684 , GRCh38.p12 chrX: 30,308,196-41,141,431 RNU6-1087P, ATP6AP2, 102 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
    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
    nsv4451246copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-38,054,739 , GRCh38.p12 chrX: 251,879-38,195,486 H3P43, CA5B, 381 more genes
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