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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
    nsv7086211copy number variation1nstd229human GRCh38 chrX: 24,003,147-24,003,680 , GRCh37.p13 chrX: 24,021,264-24,021,797 KLHL15
    nsv7086210copy number variation1nstd229human GRCh38 chrX: 23,997,843-24,004,558 , GRCh37.p13 chrX: 24,015,960-24,022,675 KLHL15
    nsv7086209copy number variation1nstd229human GRCh38 chrX: 23,997,801-24,002,600 , GRCh37.p13 chrX: 24,015,918-24,020,717 KLHL15
    nsv7086208copy number variation1nstd229human GRCh38 chrX: 23,997,108-23,997,800 , GRCh37.p13 chrX: 24,015,225-24,015,917 KLHL15
    nsv7086207copy number variation1nstd229human GRCh38 chrX: 23,992,324-24,000,619 , GRCh37.p13 chrX: 24,010,441-24,018,736 KLHL15
    nsv7086206copy number variation1nstd229human GRCh38 chrX: 23,975,812-23,983,431 , GRCh37.p13 chrX: 23,993,929-24,001,548 KLHL15
    nsv7086202copy number variation1nstd229human GRCh38 chrX: 23,907,501-24,093,100 , GRCh37.p13 chrX: 23,925,618-24,111,217 CXorf58, EIF2S3, 2 more genes
    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
    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
    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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