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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963619insertion1nstd209human GRCh38 chr8: 55,911,192-55,911,192 , GRCh37.p13 chr8: 56,823,751-56,823,751 LYN
    nsv5959072insertion1nstd209human GRCh38 chr8: 55,887,604-55,887,604 , GRCh37.p13 chr8: 56,800,163-56,800,163 LYN
    nsv5952930insertion1nstd209human GRCh38 chr8: 55,909,011-55,909,011 , GRCh37.p13 chr8: 56,821,570-56,821,570 LYN
    nsv5912615copy number variation1nstd209human GRCh38 chr8: 55,962,514-55,963,554 , GRCh37.p13 chr8: 56,875,073-56,876,113 LYN
    nsv5863264copy number variation1nstd209human GRCh38 chr8: 55,962,458-55,963,657 , GRCh37.p13 chr8: 56,875,017-56,876,216 LYN
    nsv5728972mobile element insertion2nstd211human GRCh38 chr8: 55,932,335-55,932,335 , GRCh37.p13 chr8: 56,844,894-56,844,894 LYN
    nsv5724054mobile element insertion1nstd211human GRCh38 chr8: 55,949,239-55,949,239 , GRCh37.p13 chr8: 56,861,798-56,861,798 LYN
    nsv5718154mobile element insertion2nstd211human GRCh38 chr8: 55,980,891-55,980,891 , GRCh37.p13 chr8: 56,893,450-56,893,450 RN7SL798P, LYN
    nsv5715584mobile element insertion1nstd211human GRCh38 chr8: 55,970,136-55,970,136 , GRCh37.p13 chr8: 56,882,695-56,882,695 LYN
    nsv5712149mobile element insertion1nstd211human GRCh38 chr8: 55,900,849-55,900,849 , GRCh37.p13 chr8: 56,813,408-56,813,408 LYN, SNORA1B
    nsv5703519mobile element insertion1nstd211human GRCh38 chr8: 55,886,916-55,886,916 , GRCh37.p13 chr8: 56,799,475-56,799,475 LYN
    nsv5637977insertion1nstd207human GRCh38 chr8: 55,911,102-55,911,102 , GRCh37.p13 chr8: 56,823,661-56,823,661 LYN
    nsv5631519insertion1nstd207human GRCh38 chr8: 55,900,835-55,900,835 , GRCh37.p13 chr8: 56,813,394-56,813,394 LYN, SNORA1B
    nsv5561013mobile element insertion1nstd206human GRCh38 chr8: 55,970,136-55,970,187 , GRCh37.p13 chr8: 56,882,695-56,882,746 LYN
    nsv5560707mobile element insertion1nstd206human GRCh38 chr8: 55,932,335-55,932,386 , GRCh37.p13 chr8: 56,844,894-56,844,945 LYN
    nsv5490281copy number variation1nstd206human GRCh38 chr8: 56,000,706-56,001,180 , GRCh37.p13 chr8: 56,913,265-56,913,739 LYN
    nsv5483659copy number variation1nstd206human GRCh38 chr8: 55,901,114-55,906,678 , GRCh37.p13 chr8: 56,813,673-56,819,237 LYN, SNORA1B
    nsv5481916copy number variation1nstd206human GRCh38 chr8: 55,910,907-55,940,461 , GRCh37.p13 chr8: 56,823,466-56,853,020 LYN
    nsv5476017copy number variation1nstd206human GRCh38 chr8: 55,808,595-55,967,439 , GRCh37.p13 chr8: 56,721,154-56,879,998 LYN, TGS1, 1 more genes
    nsv5405323mobile element insertion1nstd206human GRCh38 chr8: 55,886,916-55,886,967 , GRCh37.p13 chr8: 56,799,475-56,799,526 LYN
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