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Items: 1 to 20 of 483

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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
    nsv7098612copy number variation1nstd102humanUncertain significance GRCh37 chrX: 20,173,516-20,195,222 , GRCh38.p12 chrX: 20,155,398-20,177,104 RPS6KA3
    nsv7098611copy number variation1nstd102humanPathogenic GRCh37 chrX: 20,173,516-20,174,387 , GRCh38.p12 chrX: 20,155,398-20,156,269 RPS6KA3
    nsv7098359copy number variation1nstd102humanUncertain significance GRCh37 chrX: 18,525,053-20,284,750 , GRCh38.p12 chrX: 18,506,933-20,266,632 PPEF1, PDHA1, 23 more genes
    nsv7098013copy number variation1nstd102humanUncertain significance GRCh37 chrX: 20,173,516-20,252,952 , GRCh38.p12 chrX: 20,155,398-20,234,834 RPS6KA3
    nsv7086145copy number variation1nstd229human GRCh38 chrX: 20,245,075-20,248,966 , GRCh37.p13 chrX: 20,263,193-20,267,084 RPS6KA3
    nsv7086144copy number variation1nstd229human GRCh38 chrX: 20,243,019-20,244,164 , GRCh37.p13 chrX: 20,261,137-20,262,282 RPS6KA3
    nsv7086143copy number variation1nstd229human GRCh38 chrX: 20,223,456-20,223,530 , GRCh37.p13 chrX: 20,241,574-20,241,648 RPS6KA3
    nsv7086142copy number variation1nstd229human GRCh38 chrX: 20,217,227-20,219,652 , GRCh37.p13 chrX: 20,235,345-20,237,770 RPS6KA3
    nsv7086141copy number variation1nstd229human GRCh38 chrX: 20,215,301-20,229,800 , GRCh37.p13 chrX: 20,233,419-20,247,918 RPS6KA3
    nsv7086140copy number variation1nstd229human GRCh38 chrX: 20,198,507-20,700,341 , GRCh37.p13 chrX: 20,216,625-20,718,459 RN7SKP183, RPS6KA3
    nsv7086139copy number variation1nstd229human GRCh38 chrX: 20,152,201-20,154,400 , GRCh37.p13 chrX: 20,170,319-20,172,518 RPS6KA3
    nsv7086138copy number variation1nstd229human GRCh38 chrX: 20,150,987-20,151,477 , GRCh37.p13 chrX: 20,169,105-20,169,595 RPS6KA3
    nsv7086125copy number variation1nstd229human GRCh38 chrX: 20,008,238-20,358,387 , GRCh37.p13 chrX: 20,026,356-20,376,505 RPS6KA3, SCARNA9L, 4 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
    nsv7086086copy number variation1nstd229human GRCh38 chrX: 19,521,108-20,478,041 , GRCh37.p13 chrX: 19,539,226-20,496,159 LOC729609, BCLAF3, 8 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
    nsv7080097copy number variation1nstd229human GRCh38 chrX: 20,256,721-20,257,127 , GRCh37.p13 chrX: 20,274,839-20,275,245 RPS6KA3
    nsv7037605inversion1nstd229human GRCh38 chrX: 18,692,586-26,419,471 , GRCh37.p13 chrX: 18,710,705-26,437,588 PPEF1-AS1, MAP7D2, 79 more genes
    nsv7032498inversion1nstd229human GRCh38 chrX: 20,175,249-20,175,295 , GRCh37.p13 chrX: 20,193,367-20,193,413 RPS6KA3
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