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Items: 1 to 20 of 290

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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
    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
    nsv5876880copy number variation1nstd209human GRCh38 chrX: 54,752,342-54,753,281 , GRCh37.p13 chrX: 54,778,775-54,779,714 ITIH6
    nsv5873477copy number variation1nstd209human GRCh38 chrX: 54,796,404-54,796,536 , GRCh37.p13 chrX: 54,822,837-54,822,969 ITIH6
    nsv5730114mobile element insertion1nstd211human GRCh38 chrX: 54,767,362-54,767,362 , GRCh37.p13 chrX: 54,793,795-54,793,795 ITIH6
    nsv5717895mobile element insertion2nstd211human GRCh38 chrX: 54,747,390-54,747,390 , GRCh37.p13 chrX: 54,773,823-54,773,823 ITIH6
    nsv5664629copy number variation1nstd207human GRCh38 chrX: 54,765,648-54,765,712 , GRCh37.p13 chrX: 54,792,081-54,792,145 ITIH6
    nsv5563412mobile element insertion1nstd206human GRCh38 chrX: 54,767,362-54,767,413 , GRCh37.p13 chrX: 54,793,795-54,793,846 ITIH6
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5562045sequence alteration1nstd206human GRCh38 chrX: 54,788,017-54,825,346 , GRCh37.p13 chrX: 54,814,450-54,851,779 MAGED2, ITIH6, 1 more genes
    nsv5561407mobile element insertion1nstd206human GRCh38 chrX: 54,747,390-54,747,441 , GRCh37.p13 chrX: 54,773,823-54,773,874 ITIH6
    nsv5537708inversion1nstd206human GRCh38 chrX: 54,787,775-54,825,867 , GRCh37.p13 chrX: 54,814,208-54,852,300 MAGED2, ITIH6, 1 more genes
    nsv5417216copy number variation1nstd206human GRCh38 chrX: 54,775,030-54,775,086 , GRCh37.p13 chrX: 54,801,463-54,801,519 ITIH6
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5376241translocation1nstd200human GRCh38 chrX: 54,762,009-54,762,009 , GRCh38 chrX: 54,861,237-54,861,237 , GRCh37.p13 chrX: 54,788,442-54,788,442 , GRCh37.p13 chrX: 54,887,670-54,887,670 ITIH6
    nsv5194071mobile element insertion1nstd203human GRCh38 chrX: 54,779,792-54,779,806 , GRCh37.p13 chrX: 54,806,225-54,806,239 ITIH6
    nsv5187615mobile element insertion1nstd203human GRCh38 chrX: 54,747,379-54,747,390 , GRCh37.p13 chrX: 54,773,812-54,773,823 ITIH6
    nsv5185376mobile element insertion1nstd203human GRCh38 chrX: 54,765,577-54,765,614 , GRCh37.p13 chrX: 54,792,010-54,792,047 ITIH6
    nsv5183153mobile element insertion1nstd203human GRCh38 chrX: 54,747,375-54,747,390 , GRCh37.p13 chrX: 54,773,808-54,773,823 ITIH6
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
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