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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
    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
    nsv7080260copy number variation1nstd229human GRCh38 chrX: 21,964,453-22,191,653 , GRCh37.p13 chrX: 21,982,571-22,209,770 SMS, PHEX-AS1, 2 more genes
    nsv7080259copy number variation1nstd229human GRCh38 chrX: 21,949,733-21,949,938 , GRCh37.p13 chrX: 21,967,851-21,968,056 SMS
    nsv7080258copy number variation1nstd229human GRCh38 chrX: 21,933,787-22,132,358 , GRCh37.p13 chrX: 21,951,905-22,150,475 CYTH1P1, PHEX, 1 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
    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
    nsv6314527complex chromosomal rearrangement2nstd102humanPathogenic GRCh38.p12 chr8: 23,485,454-23,485,454 , GRCh38.p12 chr8: 23,479,910-23,479,910 , GRCh37 chr8: 23,337,423-23,337,423 , GRCh37 chr8: 23,342,967-23,342,967 , GRCh37 chrX: 22,004,187-22,004,187 , GRCh37 chrX: 22,009,995-22,009,995 , GRCh38.p12 chrX: 21,986,069-21,986,069 , GRCh38.p12 chrX: 21,991,877-21,991,877 SMS, LOC646708
    nsv6313406copy number variation1nstd102humanPathogenic GRCh37 chrX: 22,012,410-22,151,761 , GRCh38.p12 chrX: 21,994,292-22,133,644 SMS, PHEX
    nsv6313405copy number variation1nstd102humanPathogenic GRCh37 chrX: 21,985,294-22,196,513 , GRCh38.p12 chrX: 21,967,176-22,178,396 PHEX-AS1, PHEX, 1 more genes
    nsv6313047copy number variation1nstd102humanPathogenic GRCh37 chrX: 21,755,681-22,266,301 , GRCh38.p12 chrX: 21,737,563-22,248,184 PHEX, SMS, 6 more genes
    nsv6290611copy number variation1nstd102humanUncertain significance GRCh37 chrX: 20,760,624-22,571,267 , GRCh38.p12 chrX: 20,742,506-22,553,150 PHEX, METTL15P3, 14 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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