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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138378insertion1nstd232human GRCh37.p13 chrX: 23,693,224-23,693,224 , GRCh38.p12 chrX: 23,675,107-23,675,107 PRDX4
    nsv7138215insertion1nstd232human GRCh37.p13 chrX: 23,689,763-23,689,763 , GRCh38.p12 chrX: 23,671,646-23,671,646 PRDX4
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7086172copy number variation1nstd229human GRCh38 chrX: 23,605,777-23,734,981 , GRCh37.p13 chrX: 23,623,894-23,753,098 ACOT9, PRDX4
    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
    nsv7085539copy number variation1nstd229human GRCh38 chrX: 15,461,305-24,177,792 , GRCh37.p13 chrX: 15,479,428-24,195,909 LOC105373146, PIR-FIGF, 104 more genes
    nsv7037988inversion1nstd229human GRCh38 chrX: 22,391,325-24,781,522 , GRCh37.p13 chrX: 22,409,442-24,799,639 HIKESHIP1, ZFX-AS1, 28 more genes
    nsv7037605inversion1nstd229human GRCh38 chrX: 18,692,586-26,419,471 , GRCh37.p13 chrX: 18,710,705-26,437,588 PPEF1-AS1, MAP7D2, 79 more genes
    nsv7029948inversion1nstd229human GRCh38 chrX: 23,568,012-24,085,497 , GRCh37.p13 chrX: 23,586,129-24,103,614 PRDX4, CXorf58, 7 more genes
    nsv7026728inversion1nstd229human GRCh38 chrX: 22,131,232-24,276,641 , GRCh37.p13 chrX: 22,149,349-24,294,758 APOO, SAT1-DT, 20 more genes
    nsv6634246copy number variation1nstd224human GRCh37 chrX: 23,637,116-23,706,869 , GRCh38.p12 chrX: 23,618,999-23,688,752 PRDX4
    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
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6315330copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-57,841,304 , GRCh38.p12 chrX: 251,879-57,814,871 NPM1P9, UBE2E4P, 799 more genes
    nsv6313163copy number variation1nstd102humanUncertain significance GRCh37 chrX: 23,105,194-31,458,625 , GRCh38.p12 chrX: 23,087,077-31,440,508 H2BP7, MIR6134, 86 more genes
    nsv6137607copy number variation1nstd213human GRCh37 chrX: 4,160,000-52,130,001 , GRCh38.p12 chrX: 4,241,959-52,386,858 NR0B1, AMELX, 630 more genes
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