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Items: 1 to 20 of 411

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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
    nsv7098867copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-6,069,814 , GRCh38.p12 chrX: 284,188-6,151,773 RPL14P5, NLGN4X, 64 more genes
    nsv7076875copy number variation1nstd229human GRCh38 chrX: 4,227,585-5,220,447 , GRCh37.p13 chrX: 4,145,626-5,138,488 MTCYBP12, LOC101928201, 1 more genes
    nsv7076116copy number variation1nstd229human GRCh38 chrX: 4,332,010-5,688,105 , GRCh37.p13 chrX: 4,250,051-5,606,146 MTCYBP12, MTND6P12, 3 more genes
    nsv7074673copy number variation1nstd229human GRCh38 chrX: 4,223,338-4,936,394 , GRCh37.p13 chrX: 4,141,379-4,854,435 LOC101928201
    nsv7074484copy number variation1nstd229human GRCh38 chrX: 4,350,455-4,965,526 , GRCh37.p13 chrX: 4,268,496-4,883,567 LOC101928201
    nsv7072994copy number variation1nstd229human GRCh38 chrX: 4,549,002-4,709,767 , GRCh37.p13 chrX: 4,467,043-4,627,808 LOC101928201
    nsv7072862copy number variation1nstd229human GRCh38 chrX: 4,534,398-4,631,936 , GRCh37.p13 chrX: 4,452,439-4,549,977 LOC101928201
    nsv7070897copy number variation1nstd229human GRCh38 chrX: 4,558,052-4,711,554 , GRCh37.p13 chrX: 4,476,093-4,629,595 LOC101928201
    nsv7068357copy number variation1nstd229human GRCh38 chrX: 4,396,807-4,777,685 , GRCh37.p13 chrX: 4,314,848-4,695,726 LOC101928201
    nsv7065422copy number variation1nstd229human GRCh38 chrX: 4,580,104-4,651,470 , GRCh37.p13 chrX: 4,498,145-4,569,511 LOC101928201
    nsv7063241copy number variation1nstd229human GRCh38 chrX: 4,112,900-4,716,407 , GRCh37.p13 chrX: 4,030,941-4,634,448 LOC101928201
    nsv7063113copy number variation1nstd229human GRCh38 chrX: 4,608,792-4,628,948 , GRCh37.p13 chrX: 4,526,833-4,546,989 LOC101928201
    nsv7060963copy number variation1nstd229human GRCh38 chrX: 4,558,052-4,711,553 , GRCh37.p13 chrX: 4,476,093-4,629,594 LOC101928201
    nsv7060013copy number variation1nstd229human GRCh38 chrX: 4,224,180-4,680,602 , GRCh37.p13 chrX: 4,142,221-4,598,643 LOC101928201
    nsv7059872copy number variation1nstd229human GRCh38 chrX: 3,621,338-5,069,395 , GRCh37.p13 chrX: 3,539,379-4,987,436 FAM239B, FAM239C, 10 more genes
    nsv7059174copy number variation1nstd229human GRCh38 chrX: 4,617,801-4,633,900 , GRCh37.p13 chrX: 4,535,842-4,551,941 LOC101928201
    nsv7037404inversion1nstd229human GRCh38 chrX: 3,984,568-6,309,689 , GRCh37.p13 chrX: 3,902,609-6,227,730 LOC347381, MTND6P12, 6 more genes
    nsv6636165copy number variation1nstd102humanPathogenic GRCh37 chrX: 2,703,633-14,515,021 , GRCh38.p12 chrX: 2,785,592-14,496,899 GPX1P1, XG, 108 more genes
    nsv6636029copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,626,596-7,832,236 , GRCh38.p12 chrX: 1,507,703-7,864,195 ARSL, FAM239A, 53 more genes
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