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Items: 1 to 20 of 392

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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
    nsv7086241copy number variation1nstd229human GRCh38 chrX: 24,216,334-24,216,637 , GRCh37.p13 chrX: 24,234,451-24,234,754 ZFX
    nsv7086240copy number variation1nstd229human GRCh38 chrX: 24,214,754-24,239,754 , GRCh37.p13 chrX: 24,232,871-24,257,871 ZFX
    nsv7086239copy number variation1nstd229human GRCh38 chrX: 24,173,601-24,178,900 , GRCh37.p13 chrX: 24,191,718-24,197,017 ZFX
    nsv7086238copy number variation1nstd229human GRCh38 chrX: 24,155,601-24,164,100 , GRCh37.p13 chrX: 24,173,718-24,182,217 ZFX
    nsv7086237copy number variation1nstd229human GRCh38 chrX: 24,150,001-24,167,200 , GRCh37.p13 chrX: 24,168,118-24,185,317 ZFX, ZFX-AS1
    nsv7086236copy number variation1nstd229human GRCh38 chrX: 24,149,287-24,149,318 , GRCh37.p13 chrX: 24,167,404-24,167,435 ZFX-AS1, ZFX
    nsv7086235copy number variation1nstd229human GRCh38 chrX: 24,144,543-24,147,835 , GRCh37.p13 chrX: 24,162,660-24,165,952 ZFX, ZFX-AS1
    nsv7086201copy number variation1nstd229human GRCh38 chrX: 23,898,001-24,201,800 , GRCh37.p13 chrX: 23,916,118-24,219,917 APOO, ZFX, 4 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
    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
    nsv7031368inversion1nstd229human GRCh38 chrX: 24,203,101-24,207,488 , GRCh37.p13 chrX: 24,221,218-24,225,605 ZFX
    nsv7026728inversion1nstd229human GRCh38 chrX: 22,131,232-24,276,641 , GRCh37.p13 chrX: 22,149,349-24,294,758 APOO, SAT1-DT, 20 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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