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Items: 1 to 20 of 356

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112721copy number variation1nstd102humanPathogenic GRCh37 chrX: 47,179,068-54,424,785 , GRCh38.p12 chrX: 47,319,669-54,398,352 SNORA11E, SSX11P, 229 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
    nsv5974288copy number variation1nstd209human GRCh38 chrX: 47,391,892-47,396,699 , GRCh37.p13 chrX: 47,251,291-47,256,098 ZNF157
    nsv5882824copy number variation1nstd209human GRCh38 chrX: 44,722,720-48,672,672 , GRCh37.p13 chrX: 44,581,966-47,619,970 ZNF674-AS1, CDK16, 115 more genes
    nsv5868795copy number variation1nstd209human GRCh38 chrX: 47,392,961-47,396,741 , GRCh37.p13 chrX: 47,252,360-47,256,140 ZNF157
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5429679copy number variation1nstd206human GRCh38 chrX: 47,371,765-47,375,174 , GRCh37.p13 chrX: 47,231,164-47,234,573 ZNF157
    nsv5421337copy number variation1nstd206human GRCh38 chrX: 47,407,624-47,480,537 , GRCh37.p13 chrX: 47,267,023-47,339,936 ZNF41, NPM1P49, 1 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
    nsv5381699copy number variation1nstd102humanUncertain significance GRCh37 chrX: 46,696,536-47,436,910 , GRCh38.p12 chrX: 46,837,101-47,577,511 LINC01560, LOC105373194, 25 more genes
    nsv5194387mobile element insertion1nstd203human GRCh38 chrX: 47,397,260-47,397,260 , GRCh37.p13 chrX: 47,256,659-47,256,659 ZNF157
    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
    nsv4771375copy number variation1nstd200human GRCh37 chrX: 47,252,361-47,256,142 , GRCh38.p12 chrX: 47,392,962-47,396,743 ZNF157
    nsv4728606copy number variation1nstd102humanUncertain significance GRCh37 chrX: 46,942,052-47,379,255 , GRCh38.p12 chrX: 47,082,653-47,519,856 LOC100419232, ZNF41, 20 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
    nsv4674588copy number variation1nstd102humanPathogenic GRCh37 chrX: 539,722-55,509,385 , GRCh38.p12 chrX: 578,987-55,482,952 LOC392440, SSX4, 769 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
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