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Items: 1 to 20 of 433

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148033insertion1nstd232human GRCh37.p13 chrX: 114,871,291-114,871,291 , GRCh38.p12 chrX: 115,636,979-115,636,979 PLS3
    nsv7146417insertion1nstd232human GRCh37.p13 chrX: 114,880,860-114,880,860 , GRCh38.p12 chrX: 115,646,540-115,646,540 PLS3
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098111copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 114,871,128-114,871,310 , GRCh38.p12 chrX: 115,636,816-115,636,998 PLS3
    nsv7098110copy number variation1nstd102humanPathogenic GRCh37 chrX: 114,844,563-114,844,655 , GRCh38.p12 chrX: 115,610,251-115,610,343 PLS3
    nsv7097981copy number variation1nstd102humanPathogenic GRCh37 chrX: 114,844,563-114,883,881 , GRCh38.p12 chrX: 115,610,251-115,649,561 PLS3
    nsv7082831copy number variation1nstd229human GRCh38 chrX: 115,633,095-115,687,182 , GRCh37.p13 chrX: 114,867,407-114,921,502 , GRCh37.p13 chrX|NW_004070891.1: 1,301,897-1,355,984 PLS3, PHF5AP4, 1 more genes
    nsv7082830copy number variation1nstd229human GRCh38 chrX: 115,609,546-115,610,113 , GRCh37.p13 chrX|NW_004070891.1: 1,278,348-1,278,915 , GRCh37.p13 chrX: 114,843,858-114,844,425 PLS3
    nsv7082829copy number variation1nstd229human GRCh38 chrX: 115,603,212-115,603,559 , GRCh37.p13 chrX|NW_004070891.1: 1,272,014-1,272,361 , GRCh37.p13 chrX: 114,837,524-114,837,871 PLS3
    nsv7082828copy number variation1nstd229human GRCh38 chrX: 115,594,217-115,594,871 , GRCh37.p13 chrX: 114,828,529-114,829,183 , GRCh37.p13 chrX|NW_004070891.1: 1,263,019-1,263,673 PLS3
    nsv7082827copy number variation1nstd229human GRCh38 chrX: 115,589,448-116,387,614 , GRCh37.p13 chrX: 114,823,760-115,518,754 , GRCh37.p13 chrX|NW_004070892.1: 1-548,665 AGTR2, ASS1P5, 9 more genes
    nsv7082826copy number variation1nstd229human GRCh38 chrX: 115,589,448-116,374,411 , GRCh37.p13 chrX: 114,823,760-115,505,557 , GRCh37.p13 chrX|NW_004070892.1: 1-535,462 SUMO2P21, DANT1, 9 more genes
    nsv7082825copy number variation1nstd229human GRCh38 chrX: 115,565,795-115,573,163 , GRCh37.p13 chrX: 114,800,121-114,807,478 , GRCh37.p13 chrX|NW_004070891.1: 1,234,597-1,241,965 PLS3
    nsv7082824copy number variation1nstd229human GRCh38 chrX: 115,564,329-115,568,905 , GRCh37.p13 chrX|NW_004070891.1: 1,233,131-1,237,707 , GRCh37.p13 chrX: 114,798,655-114,803,227 PLS3
    nsv7082817copy number variation1nstd229human GRCh38 chrX: 115,510,102-115,570,867 , GRCh37.p13 chrX: 114,744,415-114,805,183 , GRCh37.p13 chrX|NW_004070891.1: 1,178,904-1,239,669 PLS3, PLS3-AS1
    nsv7082804copy number variation1nstd229human GRCh38 chrX: 115,418,070-115,967,397 , GRCh37.p13 chrX|NW_004070891.1: 1,086,872-1,389,764 , GRCh37.p13 chrX: 114,652,539-115,083,730 DANT2, ASS1P5, 8 more genes
    nsv7082791copy number variation1nstd229human GRCh38 chrX: 115,305,420-115,627,472 , GRCh37.p13 chrX|NW_004070891.1: 974,222-1,296,274 , GRCh37.p13 chrX: 114,539,985-114,861,784 LOC105373314, PLS3, 4 more genes
    nsv7082783copy number variation1nstd229human GRCh38 chrX: 115,144,540-115,620,007 , GRCh37.p13 chrX|NW_004070891.1: 813,342-1,288,809 , GRCh37.p13 chrX: 114,379,103-114,854,319 LOC107985681, LRCH2, 7 more genes
    nsv7056261inversion1nstd229human GRCh38 chrX: 115,650,539-115,657,966 , GRCh37.p13 chrX|NW_004070891.1: 1,319,341-1,326,768 , GRCh37.p13 chrX: 114,884,859-114,892,286 PLS3, PHF5AP4
    nsv7055271inversion1nstd229human GRCh38 chrX: 114,091,775-119,749,531 , GRCh37.p13 chrX: 115,732,291-118,883,494 ZCCHC12, CT47C1, 83 more genes
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