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Items: 1 to 20 of 651

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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
    nsv7079363copy number variation1nstd229human GRCh38 chrX: 141,649,601-141,652,100 , GRCh37.p13 chrX: 140,737,731-140,740,230 , GRCh37.p13 chrX|NW_004070888.1: 745,404-747,903 SPANXA2-OT1
    nsv7079362copy number variation1nstd229human GRCh38 chrX: 141,643,920-141,710,232 , GRCh37.p13 chrX|NW_004070888.1: 739,723-806,035 , GRCh37.p13 chrX: 140,732,051-140,798,388 SPANXA2-OT1, SPANXD
    nsv7079361copy number variation1nstd229human GRCh38 chrX: 141,643,371-141,643,908 , GRCh37.p13 chrX|NW_004070888.1: 739,174-739,711 , GRCh37.p13 chrX: 140,731,502-140,732,039 SPANXA2-OT1
    nsv7079360copy number variation1nstd229human GRCh38 chrX: 141,638,355-141,638,923 , GRCh37.p13 chrX|NW_004070888.1: 734,158-734,726 , GRCh37.p13 chrX: 140,726,485-140,727,053 SPANXA2-OT1
    nsv7079359copy number variation1nstd229human GRCh38 chrX: 141,638,298-141,638,774 , GRCh37.p13 chrX|NW_004070888.1: 734,101-734,577 , GRCh37.p13 chrX: 140,726,428-140,726,904 SPANXA2-OT1
    nsv7079358copy number variation1nstd229human GRCh38 chrX: 141,623,401-141,627,700 , GRCh37.p13 chrX|NW_004070888.1: 719,204-723,503 , GRCh37.p13 chrX: 140,711,529-140,715,830 SPANXA2-OT1, LOC645188
    nsv7079357copy number variation1nstd229human GRCh38 chrX: 141,620,762-141,622,277 , GRCh37.p13 chrX|NW_004070888.1: 716,565-718,080 , GRCh37.p13 chrX: 140,708,890-140,710,405 SPANXA2-OT1
    nsv7079356copy number variation1nstd229human GRCh38 chrX: 141,617,901-141,621,300 , GRCh37.p13 chrX|NW_004070888.1: 713,704-717,103 , GRCh37.p13 chrX: 140,706,029-140,709,428 SPANXA2-OT1
    nsv7079355copy number variation1nstd229human GRCh38 chrX: 141,612,801-141,643,300 , GRCh37.p13 chrX|NW_004070888.1: 708,604-739,103 , GRCh37.p13 chrX: 140,700,929-140,731,431 SPANXA2-OT1, LOC645188
    nsv7079344copy number variation1nstd229human GRCh38 chrX: 141,372,173-141,719,116 , GRCh37.p13 chrX|NW_004070888.1: 467,976-814,919 , GRCh37.p13 chrX: 140,466,330-140,807,272 SPANXA2-OT1, SPANXA2, 4 more genes
    nsv7079319copy number variation1nstd229human GRCh38 chrX: 141,190,530-141,585,642 , GRCh37.p13 chrX: 140,284,707-140,673,769 , GRCh37.p13 chrX|NW_004070888.1: 286,333-681,445 SPANXA1, SPANXC, 3 more genes
    nsv7079134copy number variation1nstd229human GRCh38 chrX: 139,434,048-142,116,322 , GRCh37.p13 chrX: 138,516,207-141,204,108 LOC101928833, CDR1, 33 more genes
    nsv7079098copy number variation1nstd229human GRCh38 chrX: 139,214,744-145,647,139 , GRCh37.p13 chrX: 138,296,906-142,299,065 LOC101928833, ATP11C, 61 more genes
    nsv7079096copy number variation1nstd229human GRCh38 chrX: 139,212,792-142,672,772 , GRCh37.p13 chrX: 138,294,954-141,760,558 ATP11C, LOC105373345, 43 more genes
    nsv7079085copy number variation1nstd229human GRCh38 chrX: 139,139,041-142,300,202 , GRCh37.p13 chrX: 138,221,203-141,387,988 LINC00632, LOC100420230, 40 more genes
    nsv7057557inversion1nstd229human GRCh38 chrX: 141,115,375-141,729,413 , GRCh37.p13 chrX|NW_004070888.1: 211,178-825,216 , GRCh37.p13 chrX: 140,209,560-140,817,596 SPANXA1, SPANXD, 9 more genes
    nsv7050440inversion1nstd229human GRCh37.p13 chrX|NW_004070888.1: 253,682-880,103 , GRCh38 chrX: 141,157,879-141,784,300 , GRCh37.p13 chrX: 140,252,077-140,872,086 SPANXA1, SPANXD, 7 more genes
    nsv7045449inversion1nstd229human GRCh38 chrX: 141,633,014-141,829,937 , GRCh37.p13 chrX|NW_004070888.1: 728,817-899,320 , GRCh37.p13 chrX: 140,721,144-140,891,303 SPANXA2-OT1, SPANXD
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