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Items: 1 to 20 of 357

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966146insertion1nstd209human GRCh38 chr3: 146,483,479-146,483,479 , GRCh37.p13 chr3: 146,201,266-146,201,266 PLSCR2
    nsv5954141insertion1nstd209human GRCh38 chr3: 146,424,976-146,424,976 , GRCh37.p13 chr3: 146,142,763-146,142,763 PLSCR2
    nsv5947588insertion1nstd209human GRCh38 chr3: 146,423,325-146,423,325 , GRCh37.p13 chr3: 146,141,112-146,141,112 PLSCR2
    nsv5891615copy number variation1nstd209human GRCh38 chr3: 146,413,565-146,413,688 , GRCh37.p13 chr3: 146,131,352-146,131,475 PLSCR2
    nsv5888733copy number variation1nstd209human GRCh38 chr3: 146,433,024-146,455,087 , GRCh37.p13 chr3: 146,150,811-146,172,874 PLSCR2
    nsv5834971copy number variation1nstd209human GRCh38 chr3: 146,432,994-146,454,636 , GRCh37.p13 chr3: 146,150,781-146,172,423 PLSCR2
    nsv5720858mobile element insertion1nstd211human GRCh38 chr3: 146,412,814-146,412,814 , GRCh37.p13 chr3: 146,130,601-146,130,601 PLSCR2
    nsv5687238mobile element insertion2nstd211human GRCh38 chr3: 146,434,476-146,434,476 , GRCh37.p13 chr3: 146,152,263-146,152,263 PLSCR2
    nsv5686972mobile element insertion2nstd211human GRCh38 chr3: 146,423,340-146,423,340 , GRCh37.p13 chr3: 146,141,127-146,141,127 PLSCR2
    nsv5677906mobile element insertion1nstd211human GRCh38 chr3: 146,427,470-146,427,470 , GRCh37.p13 chr3: 146,145,257-146,145,257 PLSCR2
    nsv5614655insertion1nstd207human GRCh38 chr3: 146,483,476-146,483,476 , GRCh37.p13 chr3: 146,201,263-146,201,263 PLSCR2
    nsv5576039copy number variation1nstd207human GRCh38 chr3: 146,480,766-146,481,129 , GRCh37.p13 chr3: 146,198,553-146,198,916 PLSCR2
    nsv5555802mobile element insertion1nstd206human GRCh38 chr3: 146,412,814-146,412,865 , GRCh37.p13 chr3: 146,130,601-146,130,652 PLSCR2
    nsv5449209copy number variation1nstd206human GRCh38 chr3: 146,480,766-146,481,132 , GRCh37.p13 chr3: 146,198,553-146,198,919 PLSCR2
    nsv5442724copy number variation1nstd206human GRCh38 chr3: 146,490,706-146,490,772 , GRCh37.p13 chr3: 146,208,493-146,208,559 PLSCR2
    nsv5411610mobile element insertion1nstd206human GRCh38 chr3: 146,427,470-146,427,521 , GRCh37.p13 chr3: 146,145,257-146,145,308 PLSCR2
    nsv5403201mobile element insertion1nstd206human GRCh38 chr3: 146,423,340-146,423,391 , GRCh37.p13 chr3: 146,141,127-146,141,178 PLSCR2
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5367083translocation1nstd200human GRCh38 chr3: 146,438,672-146,438,672 , GRCh38 chr3: 146,479,418-146,479,418 , GRCh37.p13 chr3: 146,197,205-146,197,205 , GRCh37.p13 chr3: 146,156,459-146,156,459 PLSCR2
    nsv5352005translocation1nstd200human GRCh38 chr3: 146,481,132-146,481,132 , GRCh38 chr3: 146,480,766-146,480,766 , GRCh37.p13 chr3: 146,198,553-146,198,553 , GRCh37.p13 chr3: 146,198,919-146,198,919 PLSCR2
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