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Items: 1 to 20 of 528

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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
    nsv7086101copy number variation1nstd229human GRCh38 chrX: 19,663,657-28,237,068 , GRCh37.p13 chrX: 19,681,775-28,255,185 MAGEB18, RPS6KA3, 89 more genes
    nsv7085539copy number variation1nstd229human GRCh38 chrX: 15,461,305-24,177,792 , GRCh37.p13 chrX: 15,479,428-24,195,909 LOC105373146, PIR-FIGF, 104 more genes
    nsv7080236copy number variation1nstd229human GRCh38 chrX: 21,632,301-21,653,400 , GRCh37.p13 chrX: 21,650,419-21,671,518 CNKSR2, KLHL34
    nsv7080235copy number variation1nstd229human GRCh38 chrX: 21,631,986-21,635,490 , GRCh37.p13 chrX: 21,650,104-21,653,608 CNKSR2
    nsv7080234copy number variation1nstd229human GRCh38 chrX: 21,629,617-21,672,051 , GRCh37.p13 chrX: 21,647,735-21,690,169 KLHL34, CNKSR2
    nsv7080233copy number variation1nstd229human GRCh38 chrX: 21,627,001-21,627,395 , GRCh37.p13 chrX: 21,645,119-21,645,513 CNKSR2
    nsv7080232copy number variation1nstd229human GRCh38 chrX: 21,608,639-21,608,772 , GRCh37.p13 chrX: 21,626,757-21,626,890 CNKSR2
    nsv7080231copy number variation1nstd229human GRCh38 chrX: 21,600,689-21,601,098 , GRCh37.p13 chrX: 21,618,807-21,619,216 CNKSR2
    nsv7080230copy number variation1nstd229human GRCh38 chrX: 21,597,693-21,599,915 , GRCh37.p13 chrX: 21,615,811-21,618,033 CNKSR2
    nsv7080229copy number variation1nstd229human GRCh38 chrX: 21,577,001-21,579,200 , GRCh37.p13 chrX: 21,595,119-21,597,318 CNKSR2
    nsv7080228copy number variation1nstd229human GRCh38 chrX: 21,572,801-21,574,800 , GRCh37.p13 chrX: 21,590,919-21,592,918 CNKSR2
    nsv7080227copy number variation1nstd229human GRCh38 chrX: 21,545,912-21,546,012 , GRCh37.p13 chrX: 21,564,030-21,564,130 CNKSR2
    nsv7080226copy number variation1nstd229human GRCh38 chrX: 21,542,575-21,542,781 , GRCh37.p13 chrX: 21,560,693-21,560,899 CNKSR2
    nsv7080225copy number variation1nstd229human GRCh38 chrX: 21,540,501-21,548,700 , GRCh37.p13 chrX: 21,558,619-21,566,818 CNKSR2
    nsv7080224copy number variation1nstd229human GRCh38 chrX: 21,536,691-21,539,518 , GRCh37.p13 chrX: 21,554,809-21,557,636 CNKSR2
    nsv7080223copy number variation1nstd229human GRCh38 chrX: 21,495,901-21,502,700 , GRCh37.p13 chrX: 21,514,019-21,520,818 CNKSR2
    nsv7080222copy number variation1nstd229human GRCh38 chrX: 21,485,909-21,486,115 , GRCh37.p13 chrX: 21,504,027-21,504,233 CNKSR2
    nsv7080221copy number variation1nstd229human GRCh38 chrX: 21,478,263-21,481,403 , GRCh37.p13 chrX: 21,496,381-21,499,521 CNKSR2
    nsv7080220copy number variation1nstd229human GRCh38 chrX: 21,460,701-21,464,200 , GRCh37.p13 chrX: 21,478,819-21,482,318 CNKSR2
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