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Items: 1 to 20 of 308

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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
    nsv5977098copy number variation1nstd209human GRCh38 chrX: 54,959,534-54,965,194 , GRCh37.p13 chrX: 54,985,967-54,991,627 PFKFB1
    nsv5882057copy number variation1nstd209human GRCh38 chrX: 52,862,950-55,652,570 , GRCh37.p13 chrX: 52,891,979-54,424,077 , GRCh37.p13 chrX|NW_004070877.1: 2,576,065-4,110,759 , MIRLET7F2, 64 more genes
    nsv5881237copy number variation1nstd209human GRCh38 chrX: 54,974,954-54,975,024 , GRCh37.p13 chrX: 55,001,387-55,001,457 PFKFB1
    nsv5871039copy number variation1nstd209human GRCh38 chrX: 54,957,153-54,964,152 , GRCh37.p13 chrX: 54,983,586-54,990,585 PFKFB1
    nsv5726940mobile element insertion1nstd211human GRCh38 chrX: 54,990,758-54,990,758 , GRCh37.p13 chrX: 55,017,191-55,017,191 PFKFB1
    nsv5670301copy number variation1nstd207human GRCh38 chrX: 54,968,492-54,969,192 , GRCh37.p13 chrX: 54,994,925-54,995,625 PFKFB1
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5557287mobile element insertion1nstd206human GRCh38 chrX: 54,990,758-54,990,809 , GRCh37.p13 chrX: 55,017,191-55,017,242 PFKFB1
    nsv5430410copy number variation1nstd206human GRCh38 chrX: 54,974,956-54,975,025 , GRCh37.p13 chrX: 55,001,389-55,001,458 PFKFB1
    nsv5429150copy number variation1nstd206human GRCh38 chrX: 54,956,523-54,957,781 , GRCh37.p13 chrX: 54,982,956-54,984,214 PFKFB1
    nsv5428656copy number variation1nstd206human GRCh38 chrX: 54,998,917-54,999,001 , GRCh37.p13 chrX: 55,025,350-55,025,434 APEX2, PFKFB1
    nsv5420495copy number variation1nstd206human GRCh38 chrX: 54,952,200-54,952,253 , GRCh37.p13 chrX: 54,978,633-54,978,686 PFKFB1
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5184369mobile element insertion1nstd203human GRCh38 chrX: 54,990,747-54,990,758 , GRCh37.p13 chrX: 55,017,180-55,017,191 PFKFB1
    nsv5178325mobile element insertion1nstd203human GRCh38 chrX: 54,940,893-54,940,907 , GRCh37.p13 chrX: 54,967,326-54,967,340 PFKFB1
    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
    nsv4902724copy number variation1nstd200human GRCh38 chrX: 54,956,523-54,957,781 , GRCh37.p13 chrX: 54,982,956-54,984,214 PFKFB1
    nsv4787554copy number variation1nstd200human GRCh37 chrX: 54,976,434-54,977,208 , GRCh38.p12 chrX: 54,950,001-54,950,775 PFKFB1
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