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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5920237copy number variation1nstd209human GRCh38 chr8: 85,186,673-85,186,734 , GRCh37.p13 chr8: 86,098,908-86,098,969 E2F5
    nsv5915373copy number variation1nstd209human GRCh38 chr8: 85,172,142-85,176,012 , GRCh37.p13 chr8: 86,084,377-86,088,247 E2F5-DT, E2F5
    nsv5861446copy number variation1nstd209human GRCh38 chr8: 85,173,680-85,175,479 , GRCh37.p13 chr8: 86,085,915-86,087,714 E2F5-DT, E2F5
    nsv5856153copy number variation1nstd209human GRCh38 chr8: 85,172,180-85,175,779 , GRCh37.p13 chr8: 86,084,415-86,088,014 E2F5-DT, E2F5
    nsv5568432copy number variation1nstd207human GRCh38 chr8: 85,179,851-85,180,769 , GRCh37.p13 chr8: 86,092,086-86,093,004 E2F5
    nsv5485408copy number variation1nstd206human GRCh38 chr8: 85,179,851-85,180,770 , GRCh37.p13 chr8: 86,092,086-86,093,005 E2F5
    nsv5477065copy number variation1nstd206human GRCh38 chr8: 85,172,149-85,176,013 , GRCh37.p13 chr8: 86,084,384-86,088,248 E2F5-DT, E2F5
    nsv5103720mobile element insertion1nstd203human GRCh38 chr8: 85,199,628-85,199,638 , GRCh37.p13 chr8: 86,111,863-86,111,873 E2F5
    nsv5101770mobile element insertion1nstd203human GRCh38 chr8: 85,212,918-85,212,954 , GRCh37.p13 chr8: 86,125,153-86,125,189 E2F5, RBIS
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4967535copy number variation1nstd200human GRCh38 chr8: 85,203,514-85,203,652 , GRCh37.p13 chr8: 86,115,749-86,115,887 E2F5
    nsv4967534copy number variation1nstd200human GRCh38 chr8: 85,181,918-85,182,732 , GRCh37.p13 chr8: 86,094,153-86,094,967 E2F5
    nsv4967533copy number variation1nstd200human GRCh38 chr8: 85,172,149-85,176,013 , GRCh37.p13 chr8: 86,084,384-86,088,248 E2F5-DT, E2F5
    nsv4965566copy number variation1nstd200human GRCh38 chr8: 85,178,701-85,197,848 , GRCh37.p13 chr8: 86,090,936-86,110,083 E2F5
    nsv4965540copy number variation1nstd200human GRCh38 chr8: 82,628,086-85,182,488 , GRCh37.p13 chr8: 83,540,321-86,094,723 E2F5-DT, PSMC2P2, 18 more genes
    nsv4829151copy number variation1nstd200human GRCh37 chr8: 86,090,936-86,110,083 , GRCh38.p12 chr8: 85,178,701-85,197,848 E2F5
    nsv4822259copy number variation1nstd200human GRCh37 chr8: 86,115,749-86,115,887 , GRCh38.p12 chr8: 85,203,514-85,203,652 E2F5
    nsv4822258copy number variation1nstd200human GRCh37 chr8: 86,084,384-86,088,248 , GRCh38.p12 chr8: 85,172,149-85,176,013 E2F5, E2F5-DT
    nsv4675773copy number variation1nstd102humanUncertain significance GRCh37 chr8: 85,635,587-86,553,130 , GRCh38.p12 chr8: 84,723,352-85,640,901 CA3, LRRCC1, 16 more genes
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