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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
    nsv5874018copy number variation1nstd209human GRCh38 chrX: 80,737,650-80,739,851 , GRCh37.p13 chrX: 79,993,149-79,995,350 BRWD3
    nsv5667968copy number variation1nstd207human GRCh38 chrX: 80,726,205-80,726,272 , GRCh37.p13 chrX: 79,981,704-79,981,771 BRWD3
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5551687insertion1nstd206human GRCh38 chrX: 80,721,006-80,721,006 , GRCh37.p13 chrX: 79,976,505-79,976,505 BRWD3
    nsv5432814copy number variation1nstd206human GRCh38 chrX: 80,685,702-80,686,136 , GRCh37.p13 chrX: 79,941,201-79,941,635 BRWD3
    nsv5429929copy number variation1nstd206human GRCh38 chrX: 80,713,994-80,714,099 , GRCh37.p13 chrX: 79,969,493-79,969,598 BRWD3
    nsv5428535copy number variation1nstd206human GRCh38 chrX: 80,768,093-80,772,319 , GRCh37.p13 chrX: 80,023,592-80,027,818 BRWD3
    nsv5418071copy number variation1nstd206human GRCh38 chrX: 80,790,021-80,790,207 , GRCh37.p13 chrX: 80,045,520-80,045,706 BRWD3
    nsv5376572translocation1nstd200human GRCh38 chrX: 80,714,101-80,714,101 , GRCh38 chrX: 80,714,016-80,714,016 , GRCh37.p13 chrX: 79,969,600-79,969,600 , GRCh37.p13 chrX: 79,969,515-79,969,515 BRWD3
    nsv5376571translocation1nstd200human GRCh38 chrX: 80,675,041-80,675,041 , GRCh38 chrX: 80,675,091-80,675,091 , GRCh37.p13 chrX: 79,930,590-79,930,590 , GRCh37.p13 chrX: 79,930,540-79,930,540 BRWD3
    nsv5344789translocation1nstd200human GRCh37 chrX: 79,969,600-79,969,600 , GRCh37 chrX: 79,969,515-79,969,515 , GRCh38.p12 chrX: 80,714,101-80,714,101 , GRCh38.p12 chrX: 80,714,016-80,714,016 BRWD3
    nsv5330543translocation1nstd200human GRCh37 chrX: 79,981,576-79,981,576 , GRCh37 chrX: 79,981,501-79,981,501 , GRCh38.p12 chrX: 80,726,002-80,726,002 , GRCh38.p12 chrX: 80,726,077-80,726,077 BRWD3
    nsv5198855mobile element insertion1nstd203human GRCh38 chrX: 80,779,017-80,779,032 , GRCh37.p13 chrX: 80,034,516-80,034,531 BRWD3
    nsv5186219mobile element insertion1nstd203human GRCh38 chrX: 80,711,766-80,711,766 , GRCh37.p13 chrX: 79,967,265-79,967,265 BRWD3
    nsv5180566mobile element insertion1nstd203human GRCh38 chrX: 80,780,508-80,780,523 , GRCh37.p13 chrX: 80,036,007-80,036,022 BRWD3
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv5041158mobile element deletion1nstd200human GRCh38 chrX: 80,712,287-80,713,790 , GRCh37.p13 chrX: 79,967,786-79,969,289 BRWD3
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4905675copy number variation1nstd200human GRCh38 chrX: 80,656,618-80,675,353 , GRCh37.p13 chrX: 79,912,117-79,930,852 BRWD3
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