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Items: 1 to 20 of 242

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095898copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,223,339-44,638,757 , GRCh38.p12 chr20: 43,594,699-46,010,118 ADA, CCN5, 99 more genes
    nsv7062736inversion1nstd229human GRCh38 chr20: 36,955,253-45,585,462 , GRCh37.p13 chr20: 35,583,656-44,214,101 GDAP1L1, PI3, 177 more genes
    nsv7036845copy number variation1nstd229human GRCh38 chr20: 44,672,001-44,676,200 , GRCh37.p13 chr20: 43,300,642-43,304,841 LINC01260
    nsv7031535copy number variation1nstd229human GRCh38 chr20: 44,668,301-44,669,300 , GRCh37.p13 chr20: 43,296,942-43,297,941 LINC01260
    nsv7029465copy number variation1nstd229human GRCh38 chr20: 44,668,603-44,677,006 , GRCh37.p13 chr20: 43,297,244-43,305,647 LINC01260
    nsv7027338copy number variation1nstd229human GRCh38 chr20: 44,670,730-44,673,910 , GRCh37.p13 chr20: 43,299,371-43,302,551 LINC01260
    nsv7025624copy number variation1nstd229human GRCh38 chr20: 44,667,855-44,669,268 , GRCh37.p13 chr20: 43,296,496-43,297,909 LINC01260
    nsv7023569copy number variation1nstd229human GRCh38 chr20: 44,628,160-44,660,337 , GRCh37.p13 chr20: 43,256,801-43,288,978 LINC01260, ADA
    nsv7020274copy number variation1nstd229human GRCh38 chr20: 44,671,796-44,686,844 , GRCh37.p13 chr20: 43,300,437-43,315,485 LINC01260
    nsv7020009copy number variation1nstd229human GRCh38 chr20: 44,670,317-44,676,364 , GRCh37.p13 chr20: 43,298,958-43,305,005 LINC01260
    nsv6596116inversion1nstd223human GRCh38 chr20: 36,955,253-45,585,469 , GRCh37.p13 chr20: 35,583,656-44,214,108 LOC101929863, LOC105372620, 177 more genes
    nsv6555199copy number variation1nstd223human GRCh38 chr20: 44,649,601-44,690,600 , GRCh37.p13 chr20: 43,278,242-43,319,241 ADA, LINC01260
    nsv6553140copy number variation1nstd223human GRCh38 chr20: 44,654,175-44,669,190 , GRCh37.p13 chr20: 43,282,816-43,297,831 LINC01260
    nsv6549237copy number variation1nstd223human GRCh38 chr20: 44,667,864-44,669,277 , GRCh37.p13 chr20: 43,296,505-43,297,918 LINC01260
    nsv6548654copy number variation1nstd223human GRCh38 chr20: 44,669,901-44,676,100 , GRCh37.p13 chr20: 43,298,542-43,304,741 LINC01260
    nsv6544488copy number variation1nstd223human GRCh38 chr20: 44,666,914-44,667,232 , GRCh37.p13 chr20: 43,295,555-43,295,873 LINC01260
    nsv6290315copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,985,044-48,599,046 , GRCh38.p12 chr20: 44,356,404-49,982,509 PABPC1L, LOC107985401, 170 more genes
    nsv6146637copy number variation1nstd206human GRCh38 chr20: 44,666,907-44,667,252 , GRCh37.p13 chr20: 43,295,548-43,295,893 LINC01260
    nsv6134297copy number variation1nstd213human GRCh37 chr20: 42,590,000-43,450,001 , GRCh38.p12 chr20: 43,961,360-44,821,360 ADA, OSER1, 22 more genes
    nsv6134164copy number variation1nstd213human GRCh37 chr20: 43,170,000-44,070,001 , GRCh38.p12 chr20: 44,541,359-45,441,361 PI3, SEMG2, 35 more genes
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