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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
    nsv7084205copy number variation1nstd229human GRCh38 chrX: 135,581,079-135,581,426 , GRCh37.p13 chrX|NW_004070887.1: 512,222-512,569 , GRCh37.p13 chrX: 134,715,004-134,715,351 INTS6L
    nsv7084204copy number variation1nstd229human GRCh38 chrX: 135,578,044-135,734,787 , GRCh37.p13 chrX|NW_004070887.1: 509,187-665,930 , GRCh37.p13 chrX: 134,711,969-134,903,218 MGAT2P1, ETS2P1, 5 more genes
    nsv7084203copy number variation1nstd229human GRCh38 chrX: 135,554,494-135,555,280 , GRCh37.p13 chrX|NW_004070887.1: 485,637-486,423 , GRCh37.p13 chrX: 134,688,419-134,689,205 INTS6L
    nsv7084202copy number variation1nstd229human GRCh38 chrX: 135,553,001-135,713,000 , GRCh37.p13 chrX|NW_004070887.1: 484,144-644,143 , GRCh37.p13 chrX: 134,686,926-134,846,732 SAGE3P, INTS6L, 4 more genes
    nsv7084201copy number variation1nstd229human GRCh38 chrX: 135,538,143-135,746,482 , GRCh37.p13 chrX: 134,672,068-134,914,913 , GRCh37.p13 chrX|NW_004070887.1: 469,286-677,625 SAGE4P, CT45A1, 5 more genes
    nsv7084200copy number variation1nstd229human GRCh38 chrX: 135,527,313-135,533,868 , GRCh37.p13 chrX|NW_004070887.1: 458,456-465,011 , GRCh37.p13 chrX: 134,661,238-134,667,793 INTS6L
    nsv7084199copy number variation1nstd229human GRCh38 chrX: 135,527,301-135,533,800 , GRCh37.p13 chrX|NW_004070887.1: 458,444-464,943 , GRCh37.p13 chrX: 134,661,226-134,667,725 INTS6L
    nsv7084197copy number variation1nstd229human GRCh38 chrX: 135,517,043-135,519,220 , GRCh37.p13 chrX|NW_004070887.1: 448,186-450,363 , GRCh37.p13 chrX: 134,650,968-134,653,145 INTS6L-AS1, INTS6L
    nsv7084174copy number variation1nstd229human GRCh38 chrX: 135,373,087-135,534,207 , GRCh37.p13 chrX: 134,507,012-134,668,132 , GRCh37.p13 chrX|NW_004070887.1: 304,230-465,350 RNA5SP515, INTS6L-AS1, 5 more genes
    nsv7053317inversion1nstd229human GRCh38 chrX: 135,179,664-135,609,734 , GRCh37.p13 chrX: 134,313,588-134,743,659 , GRCh37.p13 chrX|NW_004070887.1: 110,808-540,877 WDR4P1, LOC100421043, 16 more genes
    nsv7052099inversion1nstd229human GRCh38 chrX: 135,452,836-135,540,618 , GRCh37.p13 chrX|NW_004070887.1: 383,979-471,761 , GRCh37.p13 chrX: 134,586,761-134,674,543 INTS6L-AS1, WDR4P1, 1 more genes
    nsv7045748inversion1nstd229human GRCh37.p13 chrX|NW_004070887.1: 341,785-455,995 , GRCh38 chrX: 135,410,642-135,524,852 , GRCh37.p13 chrX: 134,544,567-134,658,777 WDR4P1, CROCCP1, 4 more genes
    nsv7044060inversion1nstd229human GRCh38 chrX: 134,736,748-136,484,102 , GRCh37.p13 chrX|NW_004070887.1: 1-1,045,622 , GRCh37.p13 chrX: 133,870,778-135,566,261 ETDA, SAGE3P, 57 more genes
    nsv7042727inversion1nstd229human GRCh37.p13 chrX|NW_004070887.1: 295,498-509,029 , GRCh38 chrX: 135,364,355-135,577,886 , GRCh37.p13 chrX: 134,498,280-134,711,811 LOC100506790, INTS6L-AS1, 5 more genes
    nsv7040089inversion1nstd229human GRCh37.p13 chrX|NW_004070887.1: 375,705-644,848 , GRCh38 chrX: 135,444,562-135,713,705 , GRCh37.p13 chrX: 134,578,487-134,847,438 WDR4P1, SAGE4P, 6 more genes
    nsv7039978inversion1nstd229human GRCh38 chrX: 135,536,540-135,542,517 , GRCh37.p13 chrX|NW_004070887.1: 467,683-473,660 , GRCh37.p13 chrX: 134,670,465-134,676,442 INTS6L
    nsv7039184inversion1nstd229human GRCh38 chrX: 135,461,412-135,605,282 , GRCh37.p13 chrX|NW_004070887.1: 392,555-536,425 , GRCh37.p13 chrX: 134,595,337-134,739,207 SAGE4P, WDR4P1, 3 more genes
    nsv7038253inversion1nstd229human GRCh38 chrX: 135,525,202-135,525,285 , GRCh37.p13 chrX: 134,659,127-134,659,210 , GRCh37.p13 chrX|NW_004070887.1: 456,345-456,428 INTS6L
    nsv6636407copy number variation1nstd102humanPathogenic GRCh37 chrX: 124,749,464-155,233,731 , GRCh38.p12 chrX: 125,615,468-156,004,066 RN7SKP31, LOC728470, 539 more genes
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