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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
    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
    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
    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
    nsv4905407copy number variation1nstd200human GRCh38 chrX: 39,836,122-39,853,049 , GRCh37.p13 chrX: 39,695,376-39,712,303 MIR1587
    nsv4905405copy number variation1nstd200human GRCh38 chrX: 39,716,030-40,057,929 , GRCh37.p13 chrX: 39,575,284-39,917,182 LOC105373177, LOC105373180, 6 more genes
    nsv4781950copy number variation1nstd200human GRCh37 chrX: 39,575,284-39,917,182 , GRCh38.p12 chrX: 39,716,030-40,057,929 GAPDHP1, RPS11P7, 6 more genes
    nsv4728500copy number variation1nstd102humanUncertain significance GRCh37 chrX: 39,349,074-40,119,639 , GRCh38.p12 chrX: 39,489,820-40,260,386 MIR3937, GAPDHP1, 8 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
    nsv4684016inversion1nstd191human GRCh37.p13 chrX: 32,933,886-87,244,324 , GRCh38 chrX: 32,915,769-87,989,324 , ABCB7, 816 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
    nsv4516846copy number variation1nstd166human GRCh37.p13 chrX: 38,959,999-39,717,000 , GRCh38.p12 chrX: 39,100,746-39,857,746 LOC105373178, LOC105373175, 9 more genes
    nsv4452936copy number variation1nstd102humanPathogenic GRCh37 chrX: 38,056,276-40,565,244 , GRCh38.p12 chrX: 38,197,023-40,705,992 FTLP16, LINC01283, 33 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
    nsv4436319copy number variation1nstd102humanPathogenic GRCh37 chrX: 1-47,140,860 , GRCh38.p12 chrX: 10,001-47,281,461 RNU6-266P, MID1IP1, 515 more genes
    nsv4436196copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,814-50,519,984 , GRCh38.p12 chrX: 10,814-50,776,984 CTPS2, CLTRN, 653 more genes
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