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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
    nsv7098218copy number variation1nstd102humanUncertain significance GRCh37 chrX: 118,708,675-119,761,021 , GRCh38.p12 chrX: 119,574,712-120,627,166 RHOXF2B, RHOXF1P3, 33 more genes
    nsv7098217copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 117,629,935-119,761,021 , GRCh38.p12 chrX: 118,495,972-120,627,166 HNRNPA1P28, RNU7-86P, 59 more genes
    nsv7097982copy number variation1nstd102humanUncertain significance GRCh37 chrX: 118,968,841-119,010,497 , GRCh38.p12 chrX: 119,834,878-119,876,534 UPF3B, RNF113A, 1 more genes
    nsv7083218copy number variation1nstd229human GRCh38 chrX: 119,846,101-120,000,600 , GRCh37.p13 chrX: 118,980,064-119,081,533 RHOXF1P3, UPF3B, 5 more genes
    nsv7083217copy number variation1nstd229human GRCh38 chrX: 119,845,928-119,845,998 , GRCh37.p13 chrX: 118,979,891-118,979,961 UPF3B
    nsv7083216copy number variation1nstd229human GRCh38 chrX: 119,841,301-119,948,000 , GRCh37.p13 chrX: 118,975,264-119,081,533 UPF3B, NDUFA1, 3 more genes
    nsv7083215copy number variation1nstd229human GRCh38 chrX: 119,808,987-119,824,721 , GRCh37.p13 chrX: 118,942,950-118,958,684 LOC100422368, UPF3B
    nsv7083214copy number variation1nstd229human GRCh38 chrX: 119,794,173-119,823,619 , GRCh37.p13 chrX: 118,928,136-118,957,582 LOC100422368, LOC107985694, 1 more genes
    nsv7083208copy number variation1nstd229human GRCh38 chrX: 119,748,932-120,013,756 , GRCh37.p13 chrX: 118,882,895-119,081,533 RHOXF1P2, RPL39, 11 more genes
    nsv7083197copy number variation1nstd229human GRCh38 chrX: 119,706,101-119,807,400 , GRCh37.p13 chrX: 118,840,064-118,941,363 UPF3B, LOC107985694, 3 more genes
    nsv7083190copy number variation1nstd229human GRCh38 chrX: 119,649,601-119,807,300 , GRCh37.p13 chrX: 118,783,564-118,941,263 SEPTIN6, LOC107985694, 4 more genes
    nsv7083184copy number variation1nstd229human GRCh38 chrX: 119,593,801-119,978,300 , GRCh37.p13 chrX: 118,727,764-119,081,533 NKRF, SOWAHD, 11 more genes
    nsv7083182copy number variation1nstd229human GRCh38 chrX: 119,575,201-119,955,200 , GRCh37.p13 chrX: 118,709,164-119,081,533 RPL39, MIR766, 12 more genes
    nsv7057233inversion1nstd229human GRCh38 chrX: 117,599,215-122,918,174 , GRCh37.p13 chrX: 116,733,178-122,052,027 NUDT19P1, RHOXF1P2, 89 more genes
    nsv7053551inversion1nstd229human GRCh38 chrX: 119,787,766-120,266,058 , GRCh37.p13 chrX|NW_004070886.1: 1-318,488 , GRCh37.p13 chrX: 119,081,534-119,399,913 TMEM255A, RHOXF2B, 20 more genes
    nsv7053106inversion1nstd229human GRCh38 chrX: 118,857,141-120,493,178 , GRCh37.p13 chrX: 117,991,104-119,627,033 LINC03098, RNF113A, 49 more genes
    nsv7049773inversion1nstd229human GRCh38 chrX: 118,660,648-122,841,710 , GRCh37.p13 chrX: 117,794,611-121,975,563 NUDT19P6, MRPS17P9, 83 more genes
    nsv7040757inversion1nstd229human GRCh38 chrX: 119,358,756-119,946,578 , GRCh37.p13 chrX: 118,492,719-119,080,541 NDUFA1, UBE2A, 20 more genes
    nsv7038305inversion1nstd229human GRCh38 chrX: 118,464,002-122,855,541 , GRCh37.p13 chrX: 117,597,965-121,989,394 UBE2V1P16, RNY3P16, 84 more genes
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