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Items: 1 to 20 of 329

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5903472copy number variation1nstd209human GRCh38 chr3: 32,112,226-32,112,382 , GRCh37.p13 chr3: 32,153,718-32,153,874 GPD1L
    nsv5894107copy number variation1nstd209human GRCh38 chr3: 32,162,369-32,162,650 , GRCh37.p13 chr3: 32,203,861-32,204,142 GPD1L
    nsv5891366copy number variation1nstd209human GRCh38 chr3: 32,106,471-32,106,540 , GRCh37.p13 chr3: 32,147,963-32,148,032 GPD1L
    nsv5580949copy number variation1nstd207human GRCh38 chr3: 32,112,226-32,112,382 , GRCh37.p13 chr3: 32,153,718-32,153,874 GPD1L
    nsv5571139copy number variation1nstd207human GRCh38 chr3: 32,162,369-32,162,650 , GRCh37.p13 chr3: 32,203,861-32,204,142 GPD1L
    nsv5567479copy number variation1nstd207human GRCh38 chr3: 32,160,266-32,160,596 , GRCh37.p13 chr3: 32,201,758-32,202,088 GPD1L
    nsv5451897copy number variation1nstd206human GRCh38 chr3: 32,162,385-32,162,651 , GRCh37.p13 chr3: 32,203,877-32,204,143 GPD1L
    nsv5445169copy number variation1nstd206human GRCh38 chr3: 32,112,248-32,112,360 , GRCh37.p13 chr3: 32,153,740-32,153,852 GPD1L
    nsv5440397copy number variation1nstd206human GRCh38 chr3: 32,160,294-32,160,679 , GRCh37.p13 chr3: 32,201,786-32,202,171 GPD1L
    nsv5439761copy number variation1nstd206human GRCh38 chr3: 32,129,397-32,129,819 , GRCh37.p13 chr3: 32,170,889-32,171,311 GPD1L
    nsv5389439copy number variation1nstd186human GRCh37 chr3: 32,201,828-32,202,057 , GRCh38.p12 chr3: 32,160,336-32,160,565 GPD1L
    nsv5386916copy number variation1nstd186human GRCh37 chr3: 32,201,774-32,202,128 , GRCh38.p12 chr3: 32,160,282-32,160,636 GPD1L
    nsv5382014mobile element deletion2nstd186human GRCh37 chr3: 32,203,877-32,204,143 , GRCh38.p12 chr3: 32,162,385-32,162,651 GPD1L
    nsv5381419copy number variation1nstd102humanUncertain significance GRCh37 chr3: 32,148,194-32,207,412 , GRCh38.p12 chr3: 32,106,702-32,165,920 GPD1L
    nsv5351622translocation1nstd200human GRCh38 chr3: 32,140,225-32,140,225 , GRCh38 chr3: 32,138,728-32,138,728 , GRCh37.p13 chr3: 32,180,220-32,180,220 , GRCh37.p13 chr3: 32,181,717-32,181,717 GPD1L
    nsv5351621translocation1nstd200human GRCh38 chr3: 32,128,255-32,128,255 , GRCh38 chr3: 32,138,585-32,138,585 , GRCh37.p13 chr3: 32,169,747-32,169,747 , GRCh37.p13 chr3: 32,180,077-32,180,077 GPD1L
    nsv5343913translocation1nstd200human GRCh37 chr3: 32,181,717-32,181,717 , GRCh37 chr3: 32,180,220-32,180,220 , GRCh38.p12 chr3: 32,138,728-32,138,728 , GRCh38.p12 chr3: 32,140,225-32,140,225 GPD1L
    nsv5333234translocation1nstd200human GRCh37 chr3: 32,169,747-32,169,747 , GRCh37 chr3: 32,180,077-32,180,077 , GRCh38.p12 chr3: 32,138,585-32,138,585 , GRCh38.p12 chr3: 32,128,255-32,128,255 GPD1L
    nsv5319822copy number variation1nstd204human GRCh38.p13 chr3: 32,160,050-32,160,876 , GRCh37.p13 chr3: 32,201,542-32,202,368 GPD1L
    nsv5311666copy number variation1nstd204human GRCh38.p13 chr3: 32,154,838-32,173,026 , GRCh37.p13 chr3: 32,196,330-32,214,518 GPD1L
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