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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129728mobile element insertion1nstd186human GRCh37 chrX: 71,312,620-71,312,671 , GRCh38.p12 chrX: 72,092,770-72,092,821 NHSL2
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5962671insertion1nstd209human GRCh38 chrX: 72,092,752-72,092,752 , GRCh37.p13 chrX: 71,312,602-71,312,602 NHSL2
    nsv5954381insertion1nstd209human GRCh38 chrX: 71,964,023-71,964,023 , GRCh37.p13 chrX: 71,183,873-71,183,873 NHSL2, RNU6-1078P
    nsv5880738copy number variation1nstd209human GRCh38 chrX: 69,751,799-78,490,154 , GRCh37.p13 chrX: 68,971,643-77,745,651 , MTND4P31, 183 more genes
    nsv5729031mobile element insertion2nstd211human GRCh38 chrX: 72,092,770-72,092,770 , GRCh37.p13 chrX: 71,312,620-71,312,620 NHSL2
    nsv5714500mobile element insertion1nstd211human GRCh38 chrX: 71,976,403-71,976,403 , GRCh37.p13 chrX: 71,196,253-71,196,253 NHSL2
    nsv5619644insertion1nstd207human GRCh38 chrX: 72,092,752-72,092,752 , GRCh37.p13 chrX: 71,312,602-71,312,602 NHSL2
    nsv5611127insertion1nstd207human GRCh38 chrX: 71,964,023-71,964,023 , GRCh37.p13 chrX: 71,183,873-71,183,873 NHSL2, RNU6-1078P
    nsv5563681mobile element insertion1nstd206human GRCh38 chrX: 72,092,770-72,092,821 , GRCh37.p13 chrX: 71,312,620-71,312,671 NHSL2
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5557428mobile element insertion1nstd206human GRCh38 chrX: 71,976,403-71,976,454 , GRCh37.p13 chrX: 71,196,253-71,196,304 NHSL2
    nsv5433538copy number variation1nstd206human GRCh38 chrX: 71,931,374-71,931,657 , GRCh37.p13 chrX: 71,151,224-71,151,507 NHSL2
    nsv5430447copy number variation1nstd206human GRCh38 chrX: 71,740,771-72,518,210 , GRCh37.p13 chrX: 70,960,621-71,530,833 LOC101060274, CXorf49B, 15 more genes
    nsv5430157copy number variation1nstd206human GRCh38 chrX: 72,025,686-72,026,729 , GRCh37.p13 chrX: 71,245,536-71,246,579 NHSL2
    nsv5417541copy number variation1nstd206human GRCh38 chrX: 72,085,756-72,085,846 , GRCh37.p13 chrX: 71,305,606-71,305,696 NHSL2
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5196912mobile element insertion1nstd203human GRCh38 chrX: 72,090,401-72,090,401 , GRCh37.p13 chrX: 71,310,251-71,310,251 NHSL2
    nsv5181960mobile element insertion1nstd203human GRCh38 chrX: 71,983,452-71,983,472 , GRCh37.p13 chrX: 71,203,302-71,203,322 NHSL2
    nsv5176160mobile element insertion1nstd203human GRCh38 chrX: 72,092,752-72,092,770 , GRCh37.p13 chrX: 71,312,602-71,312,620 NHSL2
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