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Items: 1 to 20 of 515

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098786copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,466,387-51,241,672 , GRCh38.p12 chrX: 46,606,952-51,498,820 LOC100419232, LOC791091, 172 more genes
    nsv7098417copy number variation2nstd102humanPathogenic GRCh37 chrX: 46,618,120-48,549,553 , GRCh38.p12 chrX: 46,758,685-48,691,162 ZNF81, LOC105373194, 84 more genes
    nsv7098318copy number variation3nstd102humanUncertain significance GRCh37 chrX: 47,001,716-50,659,607 , GRCh38.p12 chrX: 47,142,317-50,916,607 PYY3, CCDC120, 148 more genes
    nsv7098317copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,466,387-50,659,607 , GRCh38.p12 chrX: 46,606,952-50,916,607 PLP2, RN7SL262P, 160 more genes
    nsv7087905copy number variation1nstd229human GRCh38 chrX: 48,071,485-48,071,904 , GRCh37.p13 chrX: 47,930,852-47,931,271 , GRCh37.p13 chrX|NW_004070880.2: 310,914-311,333 ZNF630
    nsv7087904copy number variation1nstd229human GRCh38 chrX: 48,058,711-48,059,770 , GRCh37.p13 chrX: 47,918,100-47,919,159 , GRCh37.p13 chrX|NW_004070880.2: 298,140-299,199 ZNF630-AS1, ZNF630
    nsv7087902copy number variation1nstd229human GRCh38 chrX: 48,024,501-48,211,800 , GRCh37.p13 chrX|NW_004070880.2: 263,930-451,229 , GRCh37.p13 chrX: 47,883,895-48,071,235 RNU6-707P, SSX13P, 9 more genes
    nsv7087900copy number variation1nstd229human GRCh38 chrX: 48,016,216-48,138,440 , GRCh37.p13 chrX|NW_004070880.2: 255,645-377,869 , GRCh37.p13 chrX: 47,875,612-47,997,815 SSX6P, ZNF630-AS1, 2 more genes
    nsv7087899copy number variation1nstd229human GRCh38 chrX: 48,016,207-48,138,459 , GRCh37.p13 chrX|NW_004070880.2: 255,636-377,888 , GRCh37.p13 chrX: 47,875,603-47,997,838 ZNF630, ZNF630-AS1, 2 more genes
    nsv7087898copy number variation1nstd229human GRCh38 chrX: 48,016,081-48,138,507 , GRCh37.p13 chrX|NW_004070880.2: 255,510-377,936 , GRCh37.p13 chrX: 47,875,477-47,997,892 SSX6P, ZNF630-AS1, 2 more genes
    nsv7087897copy number variation1nstd229human GRCh38 chrX: 48,012,933-48,137,985 , GRCh37.p13 chrX|NW_004070880.2: 252,362-377,414 , GRCh37.p13 chrX: 47,872,335-47,997,362 SSX6P, ZNF630-AS1, 2 more genes
    nsv7087896copy number variation1nstd229human GRCh38 chrX: 48,007,501-48,138,300 , GRCh37.p13 chrX|NW_004070880.2: 246,930-377,729 , GRCh37.p13 chrX: 47,866,899-47,997,677 SSX6P, ZNF630-AS1, 3 more genes
    nsv7087894copy number variation1nstd229human GRCh38 chrX: 48,004,701-48,137,000 , GRCh37.p13 chrX|NW_004070880.2: 244,130-376,429 , GRCh37.p13 chrX: 47,864,099-47,996,377 SPACA5B, ZNF630, 3 more genes
    nsv7087893copy number variation1nstd229human GRCh37.p13 chrX|NW_004070880.2: 243,830-382,529 , GRCh38 chrX: 48,004,401-48,143,100 , GRCh37.p13 chrX: 47,863,799-48,002,528 ZNF630, SPACA5B, 4 more genes
    nsv7087892copy number variation1nstd229human GRCh38 chrX: 48,002,221-48,094,435 , GRCh37.p13 chrX|NW_004070880.2: 241,650-333,864 , GRCh37.p13 chrX: 47,861,620-47,953,814 SPACA5, ZNF630, 2 more genes
    nsv7087889copy number variation1nstd229human GRCh38 chrX: 47,960,343-48,364,503 , GRCh37.p13 chrX|NW_004070880.2: 199,772-603,932 , GRCh37.p13 chrX: 47,819,742-48,223,938 S100A11P5, SSX9P, 24 more genes
    nsv7087888copy number variation1nstd229human GRCh38 chrX: 47,960,301-48,363,500 , GRCh37.p13 chrX|NW_004070880.2: 199,730-602,929 , GRCh37.p13 chrX: 47,819,700-48,222,935 SSX13P, LOC100420083, 24 more genes
    nsv7087864copy number variation1nstd229human GRCh38 chrX: 47,721,810-48,192,356 , GRCh37.p13 chrX|NW_004070880.2: 1-431,785 , GRCh37.p13 chrX: 47,619,971-48,051,792 RNU6-707P, SSX13P, 15 more genes
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