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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098867copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-6,069,814 , GRCh38.p12 chrX: 284,188-6,151,773 RPL14P5, NLGN4X, 64 more genes
    nsv7076057copy number variation1nstd229human GRCh38 chrX: 3,032,384-3,032,570 , GRCh37.p13 chrX: 2,950,425-2,950,611 ARSH
    nsv7068773copy number variation1nstd229human GRCh38 chrX: 2,912,462-3,098,590 , GRCh37.p13 chrX: 2,830,503-3,016,631 ARSF, RN7SL578P, 3 more genes
    nsv7068643copy number variation1nstd229human GRCh38 chrX: 3,016,437-3,019,821 , GRCh37.p13 chrX: 2,934,478-2,937,862 ARSH
    nsv7067493copy number variation1nstd229human GRCh38 chrX: 2,980,683-3,499,331 , GRCh37.p13 chrX: 2,898,724-3,417,372 ARSF, RN7SL578P, 4 more genes
    nsv7066358copy number variation1nstd229human GRCh38 chrX: 3,014,983-3,019,008 , GRCh37.p13 chrX: 2,933,024-2,937,049 ARSH
    nsv7065847copy number variation1nstd229human GRCh38 chrX: 3,033,908-3,043,889 , GRCh37.p13 chrX: 2,951,949-2,961,930 ARSF, ARSH
    nsv7062838copy number variation1nstd229human GRCh38 chrX: 3,032,333-3,035,849 , GRCh37.p13 chrX: 2,950,374-2,953,890 ARSH
    nsv7060076copy number variation1nstd229human GRCh38 chrX: 2,998,560-3,152,591 , GRCh37.p13 chrX: 2,916,601-3,070,632 RN7SL578P, ARSF, 1 more genes
    nsv6636165copy number variation1nstd102humanPathogenic GRCh37 chrX: 2,703,633-14,515,021 , GRCh38.p12 chrX: 2,785,592-14,496,899 GPX1P1, XG, 108 more genes
    nsv6636134copy number variation1nstd102humanUncertain significance GRCh37 chrX: 2,370,150-3,027,737 , GRCh38.p12 chrX: 2,452,109-3,109,696 ZBED1, CD99P1, 13 more genes
    nsv6636115copy number variation1nstd102humanPathogenic GRCh37 chrX: 2,703,823-3,354,304 , GRCh38.p12 chrX: 2,785,782-3,436,263 LINC01546, MXRA5, 9 more genes
    nsv6636029copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,626,596-7,832,236 , GRCh38.p12 chrX: 1,507,703-7,864,195 ARSL, FAM239A, 53 more genes
    nsv6635989copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 1,932,788-9,676,331 , GRCh38.p12 chrX: 1,813,895-9,708,291 STS, ARSD, 67 more genes
    nsv6635241copy number variation1nstd227human GRCh37 chrX: 1,853,035-4,151,086 , GRCh38.p12 chrX: 1,734,142-4,233,045 ARSD, ARSL, 33 more genes
    nsv6634380copy number variation1nstd102humanPathogenic GRCh37 chrX: 2,696,691-3,666,623 , GRCh38.p12 chrX: 2,778,650-3,748,582 ASS1P4, ARSH, 15 more genes
    nsv6634248copy number variation1nstd224human GRCh37 chrX: 2,924,693-2,936,675 , GRCh38.p12 chrX: 3,006,652-3,018,634 ARSH
    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
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