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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
    nsv7082839copy number variation1nstd229human GRCh38 chrX: 115,716,404-115,720,140 , GRCh37.p13 chrX|NW_004070891.1: 1,385,206-1,388,942 , GRCh37.p13 chrX: 114,950,724-114,954,460 SUMO2P21
    nsv7082838copy number variation1nstd229human GRCh38 chrX: 115,710,892-115,718,306 , GRCh37.p13 chrX|NW_004070891.1: 1,379,694-1,387,108 , GRCh37.p13 chrX: 114,945,212-114,952,626 SUMO2P21
    nsv7082827copy number variation1nstd229human GRCh38 chrX: 115,589,448-116,387,614 , GRCh37.p13 chrX: 114,823,760-115,518,754 , GRCh37.p13 chrX|NW_004070892.1: 1-548,665 AGTR2, ASS1P5, 9 more genes
    nsv7082826copy number variation1nstd229human GRCh38 chrX: 115,589,448-116,374,411 , GRCh37.p13 chrX: 114,823,760-115,505,557 , GRCh37.p13 chrX|NW_004070892.1: 1-535,462 SUMO2P21, DANT1, 9 more genes
    nsv7082804copy number variation1nstd229human GRCh38 chrX: 115,418,070-115,967,397 , GRCh37.p13 chrX|NW_004070891.1: 1,086,872-1,389,764 , GRCh37.p13 chrX: 114,652,539-115,083,730 DANT2, ASS1P5, 8 more genes
    nsv7055271inversion1nstd229human GRCh38 chrX: 114,091,775-119,749,531 , GRCh37.p13 chrX: 115,732,291-118,883,494 ZCCHC12, CT47C1, 83 more genes
    nsv7053216inversion1nstd229human GRCh38 chrX: 114,054,506-118,815,100 , GRCh37.p13 chrX: 113,297,697-115,918,761 LUZP4, LOC107985681, 57 more genes
    nsv7048914inversion1nstd229human GRCh38 chrX: 113,754,776-118,814,265 , GRCh37.p13 chrX: 112,998,052-115,918,761 RN7SL712P, SLC6A14, 61 more genes
    nsv7048750inversion1nstd229human GRCh38 chrX: 114,054,489-118,815,074 , GRCh37.p13 chrX: 113,297,680-115,918,761 CT83, MIR1912, 57 more genes
    nsv7048375inversion1nstd229human GRCh38 chrX: 113,143,339-118,246,278 , GRCh37.p13 chrX: 112,386,567-117,380,241 RNU6-154P, HSPA8P7, 58 more genes
    nsv6636543copy number variation1nstd102humanPathogenic GRCh37 chrX: 93,805,850-118,913,329 , GRCh38.p12 chrX: 94,550,851-119,779,366 TRPC5OS, LOC105373314, 351 more genes
    nsv6634329copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,794,355-119,282,836 , GRCh38.p12 chrX: 77,538,874-120,148,930 NXF4, RHOXF1P1, 489 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634047copy number variation1nstd224human GRCh37 chrX: 114,871,655-114,958,974 , GRCh38.p12 chrX: 115,637,343-115,842,641 ASS1P5, PLS3, 5 more genes
    nsv6315429copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,670,699-155,233,731 , GRCh38.p12 chrX: 78,415,202-156,004,066 H2AB1, GPR174, 1081 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
    nsv6315332copy number variation1nstd102humanPathogenic GRCh37 chrX: 62,685,885-155,233,731 , GRCh38.p12 chrX: 63,466,005-156,004,066 MAGT1, TAFAZZIN, 1337 more genes
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
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