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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921736copy number variation1nstd209human GRCh38 chr11: 47,252,391-47,253,087 , GRCh37.p13 chr11: 47,273,942-47,274,638 NR1H3
    nsv5710485mobile element insertion1nstd211human GRCh38 chr11: 47,256,671-47,256,671 , GRCh37.p13 chr11: 47,278,222-47,278,222 NR1H3
    nsv5513778copy number variation1nstd206human GRCh38 chr11: 47,252,389-47,253,108 , GRCh37.p13 chr11: 47,273,940-47,274,659 NR1H3
    nsv5495054copy number variation1nstd206human GRCh38 chr11: 47,252,527-47,252,827 , GRCh37.p13 chr11: 47,274,078-47,274,378 NR1H3
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5380725copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218 MIR4688, LOC112268075, 58 more genes
    nsv5302408copy number variation1nstd204human GRCh38.p13 chr11: 47,252,413-47,253,074 , GRCh37.p13 chr11: 47,273,964-47,274,625 NR1H3
    nsv4984472copy number variation1nstd200human GRCh38 chr11: 47,263,715-47,266,480 , GRCh37.p13 chr11: 47,285,266-47,288,031 NR1H3
    nsv4841786copy number variation1nstd200human GRCh37 chr11: 47,272,621-47,273,056 , GRCh38.p12 chr11: 47,251,070-47,251,505 NR1H3
    nsv4835146copy number variation1nstd200human GRCh37 chr11: 47,273,955-47,274,622 , GRCh38.p12 chr11: 47,252,404-47,253,071 NR1H3
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4732366copy number variation1nstd199human GRCh37 chr11: 47,277,083-47,277,142 , GRCh38.p12 chr11: 47,255,532-47,255,591 NR1H3
    nsv4527683copy number variation1nstd166human GRCh37.p13 chr11: 47,288,010-47,288,256 , GRCh38.p12 chr11: 47,266,459-47,266,705 NR1H3
    nsv4201558copy number variation1nstd166human GRCh37.p13 chr11: 47,285,267-47,288,030 , GRCh38.p12 chr11: 47,263,716-47,266,479 NR1H3
    nsv3924778copy number variation1nstd102humanPathogenic GRCh38 chr11: 41,118,322-48,643,003 , GRCh37 chr11: 41,139,872-48,664,555 , NCBI36 chr11: 41,096,448-48,621,131 F2, PSMC3, 140 more genes
    nsv3919311copy number variation1nstd102humanPathogenic NCBI36 chr11: 47,188,786-47,405,458 , GRCh37 chr11: 47,232,210-47,448,882 , GRCh38 chr11: 47,210,659-47,427,331 MADD-AS1, PSMC3, 8 more genes
    nsv3914709copy number variation1nstd102humanPathogenic GRCh38 chr11: 46,840,454-48,643,003 , GRCh37 chr11: 46,862,005-48,664,555 , NCBI36 chr11: 46,818,581-48,621,131 CELF1, C1QTNF4, 56 more genes
    nsv3914563copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 42,705,681-49,113,863 , GRCh37 chr11: 42,749,105-49,157,287 , GRCh38 chr11: 42,727,555-49,135,735 ACP2, ARHGAP1, 143 more genes
    nsv3913842copy number variation1nstd102humanPathogenic GRCh37 chr11: 39,200,802-49,157,287 , NCBI36 chr11: 39,157,378-49,113,863 , GRCh38 chr11: 39,179,252-49,135,735 MIR3160-1, RPS20P26, 162 more genes
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