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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140993copy number variation1nstd232human GRCh37.p13 chrX: 114,360,011-114,360,136 , GRCh38.p12 chrX: 115,125,448-115,125,573 LRCH2, SNORA35B
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7082774copy number variation1nstd229human GRCh38 chrX: 115,043,024-115,141,940 , GRCh37.p13 chrX|NW_004070891.1: 711,826-810,742 , GRCh37.p13 chrX: 114,277,587-114,376,503 TMSB4XP7, YAP1P2, 3 more genes
    nsv7082769copy number variation1nstd229human GRCh38 chrX: 115,008,958-115,349,261 , GRCh37.p13 chrX|NW_004070891.1: 677,760-1,018,063 , GRCh37.p13 chrX: 114,243,521-114,583,909 RBMXL3, SNORA35B, 9 more genes
    nsv7082766copy number variation1nstd229human GRCh38 chrX: 114,967,276-115,163,566 , GRCh37.p13 chrX|NW_004070891.1: 636,078-832,368 , GRCh37.p13 chrX: 114,201,839-114,398,129 LRCH2, RNU6-648P, 5 more genes
    nsv7082752copy number variation1nstd229human GRCh38 chrX: 114,787,493-115,300,260 , GRCh37.p13 chrX|NW_004070891.1: 456,295-969,062 , GRCh37.p13 chrX: 114,022,056-114,534,826 LOC105373313, LRCH2, 11 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
    nsv6635277copy number variation1nstd227human GRCh37 chrX: 114,205,618-114,395,131 , GRCh38.p12 chrX: 114,971,055-115,160,568 IL13RA2, TMSB4XP7, 5 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
    nsv6634046copy number variation3nstd224human GRCh37 chrX: 114,216,163-114,395,131 , GRCh38.p12 chrX: 114,981,600-115,160,568 IL13RA2, TMSB4XP7, 5 more genes
    nsv6633958copy number variation1nstd224human GRCh37 chrX: 114,205,618-114,395,131 , GRCh38.p12 chrX: 114,971,055-115,160,568 IL13RA2, TMSB4XP7, 5 more genes
    nsv6633749copy number variation2nstd224human GRCh37 chrX: 114,205,618-114,399,364 , GRCh38.p12 chrX: 114,971,055-115,164,801 IL13RA2, TMSB4XP7, 5 more genes
    nsv6633570copy number variation1nstd224human GRCh37 chrX: 114,214,478-114,399,364 , GRCh38.p12 chrX: 114,979,915-115,164,801 IL13RA2, TMSB4XP7, 5 more genes
    nsv6633565copy number variation1nstd224human GRCh37 chrX: 107,804,808-114,879,367 , GRCh38.p12 chrX: 108,561,578-115,645,047 DCX, IL13RA2, 80 more genes
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