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Items: 1 to 20 of 1338

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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
    nsv7090810copy number variation1nstd229human GRCh38 chrX: 125,204,306-125,205,053 , GRCh37.p13 chrX: 124,338,155-124,338,902 TENM1
    nsv7090809copy number variation1nstd229human GRCh38 chrX: 125,203,101-125,204,400 , GRCh37.p13 chrX: 124,336,950-124,338,249 TENM1
    nsv7090808copy number variation1nstd229human GRCh38 chrX: 125,188,801-125,194,200 , GRCh37.p13 chrX: 124,322,650-124,328,049 TENM1
    nsv7090807copy number variation1nstd229human GRCh38 chrX: 125,173,912-125,568,021 , GRCh37.p13 chrX: 124,307,761-124,701,870 TENM1, FBLIM1P1, 1 more genes
    nsv7090806copy number variation1nstd229human GRCh38 chrX: 125,162,501-125,202,400 , GRCh37.p13 chrX: 124,296,350-124,336,249 TENM1
    nsv7090805copy number variation1nstd229human GRCh38 chrX: 125,162,001-125,177,100 , GRCh37.p13 chrX: 124,295,850-124,310,949 TENM1
    nsv7090804copy number variation1nstd229human GRCh38 chrX: 125,160,601-125,202,400 , GRCh37.p13 chrX: 124,294,450-124,336,249 TENM1
    nsv7090803copy number variation1nstd229human GRCh38 chrX: 125,157,996-125,160,554 , GRCh37.p13 chrX: 124,291,845-124,294,403 TENM1
    nsv7090802copy number variation1nstd229human GRCh38 chrX: 125,134,059-125,171,774 , GRCh37.p13 chrX: 124,267,908-124,305,623 TENM1
    nsv7090801copy number variation1nstd229human GRCh38 chrX: 125,134,047-125,170,445 , GRCh37.p13 chrX: 124,267,896-124,304,294 TENM1
    nsv7090800copy number variation1nstd229human GRCh38 chrX: 125,131,297-125,132,031 , GRCh37.p13 chrX: 124,265,146-124,265,880 TENM1
    nsv7090799copy number variation1nstd229human GRCh38 chrX: 125,131,293-125,133,513 , GRCh37.p13 chrX: 124,265,142-124,267,362 TENM1
    nsv7090798copy number variation1nstd229human GRCh38 chrX: 125,114,401-125,117,700 , GRCh37.p13 chrX: 124,248,250-124,251,549 TENM1
    nsv7090797copy number variation1nstd229human GRCh38 chrX: 125,105,322-125,109,172 , GRCh37.p13 chrX: 124,239,171-124,243,021 TENM1
    nsv7090796copy number variation1nstd229human GRCh38 chrX: 125,104,672-125,173,546 , GRCh37.p13 chrX: 124,238,521-124,307,395 TENM1
    nsv7090795copy number variation1nstd229human GRCh38 chrX: 125,100,296-125,102,452 , GRCh37.p13 chrX: 124,234,145-124,236,301 TENM1
    nsv7090794copy number variation1nstd229human GRCh38 chrX: 125,098,601-125,102,500 , GRCh37.p13 chrX: 124,232,450-124,236,349 TENM1
    nsv7090793copy number variation1nstd229human GRCh38 chrX: 125,070,630-125,101,364 , GRCh37.p13 chrX: 124,204,479-124,235,213 TENM1
    nsv7090792copy number variation1nstd229human GRCh38 chrX: 125,066,483-125,066,532 , GRCh37.p13 chrX: 124,200,332-124,200,381 TENM1
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