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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137431insertion1nstd232human GRCh37.p13 chrX: 108,906,633-108,906,633 , GRCh38.p12 chrX: 109,663,404-109,663,404 ACSL4
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7082249copy number variation1nstd229human GRCh38 chrX: 109,724,461-109,725,099 , GRCh37.p13 chrX: 108,967,690-108,968,328 ACSL4
    nsv7082248copy number variation1nstd229human GRCh38 chrX: 109,715,719-109,718,905 , GRCh37.p13 chrX: 108,958,948-108,962,134 ACSL4
    nsv7082247copy number variation1nstd229human GRCh38 chrX: 109,713,265-109,713,428 , GRCh37.p13 chrX: 108,956,494-108,956,657 ACSL4
    nsv7082246copy number variation1nstd229human GRCh38 chrX: 109,697,719-109,699,907 , GRCh37.p13 chrX: 108,940,948-108,943,136 ACSL4
    nsv7082245copy number variation1nstd229human GRCh38 chrX: 109,690,354-110,095,777 , GRCh37.p13 chrX: 108,933,583-109,339,005 MIR3978, MIR652, 4 more genes
    nsv7078498copy number variation1nstd229human GRCh38 chrX: 109,678,701-110,154,100 , GRCh37.p13 chrX: 108,921,930-109,397,328 MIR652, MIR3978, 4 more genes
    nsv7078497copy number variation1nstd229human GRCh38 chrX: 109,657,720-109,659,082 , GRCh37.p13 chrX: 108,900,949-108,902,311 ACSL4
    nsv7078496copy number variation1nstd229human GRCh38 chrX: 109,652,135-109,652,521 , GRCh37.p13 chrX: 108,895,364-108,895,750 ACSL4
    nsv7078495copy number variation1nstd229human GRCh38 chrX: 109,640,701-109,643,900 , GRCh37.p13 chrX: 108,883,930-108,887,129 ACSL4
    nsv7078494copy number variation1nstd229human GRCh38 chrX: 109,640,564-109,640,978 , GRCh37.p13 chrX: 108,883,793-108,884,207 ACSL4
    nsv7078491copy number variation1nstd229human GRCh38 chrX: 109,594,401-109,685,500 , GRCh37.p13 chrX: 108,837,630-108,928,729 ACSL4, PPP6CP, 1 more genes
    nsv7078472copy number variation1nstd229human GRCh38 chrX: 109,366,788-109,796,051 , GRCh37.p13 chrX: 108,610,017-109,039,280 LOC105373311, NXT2, 5 more genes
    nsv7078409copy number variation1nstd229human GRCh38 chrX: 109,004,896-109,765,797 , GRCh37.p13 chrX: 108,248,126-109,009,026 GUCY2F, PPP6CP, 5 more genes
    nsv7052621inversion1nstd229human GRCh38 chrX: 103,826,879-110,334,422 , GRCh37.p13 chrX: 103,081,809-109,577,650 CSGALNACT2P2, LOC107985662, 82 more genes
    nsv7044993inversion1nstd229human GRCh38 chrX: 104,618,913-113,302,073 , GRCh37.p13 chrX: 103,863,594-112,545,300 NCBP2L, TEX13B, 92 more genes
    nsv7041719inversion1nstd229human GRCh38 chrX: 105,592,744-110,464,662 , GRCh37.p13 chrX: 104,836,737-109,707,890 LOC105373312, PPP6CP, 59 more genes
    nsv6636712copy number variation1nstd102humanPathogenic GRCh37 chrX: 108,922,296-111,549,785 , GRCh38.p12 chrX: 109,679,067-112,306,557 M6PRP1, HMGB1P12, 27 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
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