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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
    nsv7148140copy number variation1nstd102humanPathogenic GRCh38 chrX: 23,730,430-32,849,918 , GRCh37.p13 chrX: 23,748,547-32,868,035 ARX, LOC107985632, 85 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7091316copy number variation1nstd229human GRCh38 chrX: 26,008,601-26,759,000 , GRCh37.p13 chrX: 26,026,718-26,777,117 MAGEB18, HMGA1P1, 10 more genes
    nsv7086384copy number variation1nstd229human GRCh38 chrX: 26,560,948-26,646,966 , GRCh37.p13 chrX: 26,579,065-26,665,083 VENTXP1
    nsv7086375copy number variation1nstd229human GRCh38 chrX: 25,891,683-26,634,692 , GRCh37.p13 chrX: 25,909,800-26,652,809 LOC100420245, LOC100422209, 8 more genes
    nsv7086366copy number variation1nstd229human GRCh38 chrX: 25,787,825-26,793,613 , GRCh37.p13 chrX: 25,805,942-26,811,730 VENTXP8, RPL7P58, 12 more genes
    nsv7086101copy number variation1nstd229human GRCh38 chrX: 19,663,657-28,237,068 , GRCh37.p13 chrX: 19,681,775-28,255,185 MAGEB18, RPS6KA3, 89 more genes
    nsv7080605copy number variation1nstd229human GRCh38 chrX: 26,506,342-26,816,878 , GRCh37.p13 chrX: 26,524,459-26,834,995 RNU1-142P, HMGA1P1, 3 more genes
    nsv7080601copy number variation1nstd229human GRCh38 chrX: 26,482,393-26,637,383 , GRCh37.p13 chrX: 26,500,510-26,655,500 VENTXP8, VENTXP1, 1 more genes
    nsv7080600copy number variation1nstd229human GRCh38 chrX: 26,472,429-26,559,020 , GRCh37.p13 chrX: 26,490,546-26,577,137 FMN2P1, VENTXP1, 1 more genes
    nsv7080599copy number variation1nstd229human GRCh38 chrX: 26,465,589-26,696,697 , GRCh37.p13 chrX: 26,483,706-26,714,814 VENTXP1, FMN2P1, 2 more genes
    nsv7080562copy number variation1nstd229human GRCh38 chrX: 26,146,788-26,808,443 , GRCh37.p13 chrX: 26,164,905-26,826,560 LOC100130052, MAGEB6, 10 more genes
    nsv7080561copy number variation1nstd229human GRCh38 chrX: 26,146,788-26,793,272 , GRCh37.p13 chrX: 26,164,905-26,811,389 MAGEB5, FMN2P1, 10 more genes
    nsv7080559copy number variation1nstd229human GRCh38 chrX: 26,129,076-26,660,004 , GRCh37.p13 chrX: 26,147,193-26,678,121 VENTXP1, MAGEB5, 8 more genes
    nsv6636147copy number variation1nstd102humanPathogenic GRCh37 chrX: 24,879,855-32,902,136 , GRCh38.p12 chrX: 24,861,738-32,884,019 RNA5SP500, MAGEB6, 64 more genes
    nsv6636122copy number variation1nstd102humanPathogenic GRCh37 chrX: 24,675,165-31,490,279 , GRCh38.p12 chrX: 24,657,048-31,472,162 SCARNA23, CKS1BP6, 65 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634135copy number variation1nstd224human GRCh37 chrX: 2,700,157-26,836,730 , GRCh38.p12 chrX: 2,782,116-26,818,613 AMELX, ARSF, 258 more genes
    nsv6315577complex substitution1nstd102humanPathogenic GRCh37 chrX: 590,376-56,315,041 , GRCh38.p12 chrX: 629,641-56,288,608 ACTG1P10, NR0B1, 778 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
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