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Items: 1 to 20 of 345

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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
    nsv7098869copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,586,015-154,774,957 , GRCh38.p12 chrX: 140,503,850-155,545,296 MAGEA6, LOC101928832, 303 more genes
    nsv7084820copy number variation1nstd229human GRCh38 chrX: 145,248,131-145,256,406 , GRCh37.p13 chrX: 144,329,651-144,337,926 , GRCh37.p13 chrX|NW_004070890.2: 772,524-780,799 SPANXN1
    nsv7084819copy number variation1nstd229human GRCh38 chrX: 145,246,150-145,250,949 , GRCh37.p13 chrX: 144,327,670-144,332,469 , GRCh37.p13 chrX|NW_004070890.2: 770,543-775,342 SPANXN1
    nsv7084818copy number variation1nstd229human GRCh38 chrX: 145,245,101-145,400,500 , GRCh37.p13 chrX: 144,326,621-144,482,018 , GRCh37.p13 chrX|NW_004070890.2: 769,494-924,891 SPANXN1
    nsv7084816copy number variation1nstd229human GRCh38 chrX: 145,219,431-145,263,109 , GRCh37.p13 chrX|NW_004070890.2: 743,824-787,502 , GRCh37.p13 chrX: 144,300,951-144,344,629 SPANXN1
    nsv7084815copy number variation1nstd229human GRCh38 chrX: 145,217,560-145,271,952 , GRCh37.p13 chrX: 144,299,080-144,353,472 , GRCh37.p13 chrX|NW_004070890.2: 741,953-796,345 SPANXN1
    nsv7084814copy number variation1nstd229human GRCh38 chrX: 145,213,629-145,307,206 , GRCh37.p13 chrX|NW_004070890.2: 738,022-831,598 , GRCh37.p13 chrX: 144,295,149-144,388,725 SPANXN1
    nsv7084813copy number variation1nstd229human GRCh38 chrX: 145,206,137-145,640,436 , GRCh37.p13 chrX|NW_004070890.2: 730,530-1,164,827 , GRCh37.p13 chrX: 144,287,657-144,721,954 SPANXN1, TRMT1P1
    nsv7084812copy number variation1nstd229human GRCh38 chrX: 145,204,110-145,276,448 , GRCh37.p13 chrX|NW_004070890.2: 728,503-800,841 , GRCh37.p13 chrX: 144,285,630-144,357,968 SPANXN1
    nsv7084808copy number variation1nstd229human GRCh38 chrX: 145,182,103-145,347,117 , GRCh37.p13 chrX|NW_004070890.2: 706,496-871,508 , GRCh37.p13 chrX: 144,263,623-144,428,635 SPANXN1
    nsv7084806copy number variation1nstd229human GRCh38 chrX: 145,168,347-145,258,328 , GRCh37.p13 chrX|NW_004070890.2: 692,740-782,721 , GRCh37.p13 chrX: 144,249,867-144,339,848 SPANXN1, CYCSP44
    nsv7084804copy number variation1nstd229human GRCh38 chrX: 145,150,130-145,639,527 , GRCh37.p13 chrX|NW_004070890.2: 674,523-1,163,918 , GRCh37.p13 chrX: 144,231,650-144,721,045 SPANXN1, CYCSP44, 1 more genes
    nsv7084799copy number variation1nstd229human GRCh38 chrX: 145,124,459-145,776,494 , GRCh37.p13 chrX: 144,205,979-144,858,012 , GRCh37.p13 chrX|NW_004070890.2: 648,852-1,300,885 SPANXN1, CYCSP44, 2 more genes
    nsv7084789copy number variation1nstd229human GRCh38 chrX: 145,080,471-145,399,199 , GRCh37.p13 chrX: 144,161,991-144,480,717 , GRCh37.p13 chrX|NW_004070890.2: 604,864-923,590 SPANXN1, CYCSP44
    nsv7084770copy number variation1nstd229human GRCh38 chrX: 144,961,509-145,329,694 , GRCh37.p13 chrX: 144,043,029-144,411,212 , GRCh37.p13 chrX|NW_004070890.2: 485,902-854,085 SPANXN1, CYCSP44, 1 more genes
    nsv7084769copy number variation1nstd229human GRCh38 chrX: 144,953,309-145,432,106 , GRCh37.p13 chrX|NW_004070890.2: 477,702-956,497 , GRCh37.p13 chrX: 144,034,829-144,513,624 RN7SKP189, CYCSP44, 1 more genes
    nsv7084767copy number variation1nstd229human GRCh38 chrX: 144,942,612-145,304,974 , GRCh37.p13 chrX|NW_004070890.2: 467,005-829,366 , GRCh37.p13 chrX: 144,024,132-144,386,493 CYCSP44, RN7SKP189, 1 more genes
    nsv7084761copy number variation1nstd229human GRCh38 chrX: 144,918,447-145,352,498 , GRCh37.p13 chrX: 143,999,967-144,434,016 , GRCh37.p13 chrX|NW_004070890.2: 442,840-876,889 SPANXN1, RN7SKP189, 1 more genes
    nsv7084735copy number variation1nstd229human GRCh37.p13 chrX|NW_004070890.2: 273,128-1,421,161 , GRCh38 chrX: 144,748,734-145,896,770 , GRCh37.p13 chrX: 143,830,255-144,978,288 HNRNPCP10, UFM1P1, 6 more genes
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