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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
    nsv5953791insertion1nstd209human GRCh38 chrX: 77,716,319-77,716,319 , GRCh37.p13 chrX|NW_003871101.3: 273,581-273,581 , GRCh37.p13 chrX: 76,971,791-76,971,791 ATRX
    nsv5951199insertion1nstd209human GRCh38 chrX: 77,651,217-77,651,217 , GRCh37.p13 chrX|NW_003871101.3: 208,479-208,479 , GRCh37.p13 chrX: 76,906,707-76,906,707 ATRX
    nsv5887446copy number variation1nstd209human GRCh38 chrX: 77,509,431-77,513,969 , GRCh37.p13 chrX|NW_003871101.3: 66,693-71,231 , GRCh37.p13 chrX: 76,764,909-76,769,447 ATRX
    nsv5880738copy number variation1nstd209human GRCh38 chrX: 69,751,799-78,490,154 , GRCh37.p13 chrX: 68,971,643-77,745,651 , MTND4P31, 183 more genes
    nsv5874684copy number variation1nstd209human GRCh38 chrX: 77,590,236-77,593,538 , GRCh37.p13 chrX: 76,845,706-76,849,008 , GRCh37.p13 chrX|NW_003871101.3: 147,498-150,800 ATRX
    nsv5729844mobile element insertion1nstd211human GRCh38 chrX: 77,568,395-77,568,395 , GRCh37.p13 chrX: 76,823,860-76,823,860 , GRCh37.p13 chrX|NW_003871101.3: 125,657-125,657 ATRX
    nsv5724861mobile element insertion1nstd211human GRCh38 chrX: 77,729,142-77,729,142 , GRCh37.p13 chrX: 76,984,620-76,984,620 , GRCh37.p13 chrX|NW_003871101.3: 286,404-286,404 ATRX
    nsv5715000mobile element insertion1nstd211human GRCh38 chrX: 77,653,002-77,653,002 , GRCh37.p13 chrX|NW_003871101.3: 210,264-210,264 , GRCh37.p13 chrX: 76,908,492-76,908,492 ATRX
    nsv5674118copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,937,002-76,940,508 , GRCh38.p12 chrX: 77,681,510-77,685,016 ATRX
    nsv5674117copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,759,356-77,042,755 , GRCh38.p12 chrX: 77,503,878-77,787,277 ATRX, FABP5P15
    nsv5665464copy number variation1nstd207human GRCh38 chrX: 77,735,472-77,735,681 , GRCh37.p13 chrX|NW_003871101.3: 292,734-292,943 , GRCh37.p13 chrX: 76,990,945-76,991,162 ATRX
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5560647mobile element insertion1nstd206human GRCh38 chrX: 77,568,395-77,568,446 , GRCh37.p13 chrX|NW_003871101.3: 125,657-125,708 , GRCh37.p13 chrX: 76,823,860-76,823,911 ATRX
    nsv5431191copy number variation1nstd206human GRCh38 chrX: 77,509,411-77,513,990 , GRCh37.p13 chrX|NW_003871101.3: 66,673-71,252 , GRCh37.p13 chrX: 76,764,889-76,769,468 ATRX
    nsv5429938copy number variation1nstd206human GRCh38 chrX: 77,625,975-77,626,194 , GRCh37.p13 chrX: 76,881,443-76,881,680 , GRCh37.p13 chrX|NW_003871101.3: 183,237-183,456 ATRX
    nsv5428426copy number variation1nstd206human GRCh38 chrX: 77,590,239-77,593,539 , GRCh37.p13 chrX|NW_003871101.3: 147,501-150,801 , GRCh37.p13 chrX: 76,845,709-76,849,009 ATRX
    nsv5425635copy number variation1nstd206human GRCh38 chrX: 77,625,617-77,626,046 , GRCh37.p13 chrX|NW_003871101.3: 182,879-183,308 , GRCh37.p13 chrX: 76,881,085-76,881,514 ATRX
    nsv5420690copy number variation1nstd206human GRCh38 chrX: 77,758,159-77,774,406 , GRCh37.p13 chrX|NW_003871101.3: 315,421-331,668 , GRCh37.p13 chrX: 77,013,640-77,029,888 ATRX
    nsv5419735copy number variation1nstd206human GRCh38 chrX: 77,608,116-77,611,615 , GRCh37.p13 chrX|NW_003871101.3: 165,378-168,877 , GRCh37.p13 chrX: 76,863,587-76,867,086 ATRX
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