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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5909773copy number variation1nstd209human GRCh38 chr8: 66,902,127-66,902,187 , GRCh37.p13 chr8: 67,814,362-67,814,422 MCMDC2
    nsv5717945mobile element insertion1nstd211human GRCh38 chr8: 66,899,044-66,899,044 , GRCh37.p13 chr8: 67,811,279-67,811,279 MCMDC2
    nsv5717774mobile element insertion1nstd211human GRCh38 chr8: 66,896,537-66,896,537 , GRCh37.p13 chr8: 67,808,772-67,808,772 MCMDC2
    nsv5643213insertion1nstd207human GRCh38 chr8: 66,911,611-66,911,611 , GRCh37.p13 chr8: 67,823,846-67,823,846 MCMDC2
    nsv5563664mobile element insertion1nstd206human GRCh38 chr8: 66,899,044-66,899,095 , GRCh37.p13 chr8: 67,811,279-67,811,330 MCMDC2
    nsv5563662mobile element insertion1nstd206human GRCh38 chr8: 66,896,537-66,896,588 , GRCh37.p13 chr8: 67,808,772-67,808,823 MCMDC2
    nsv5560573sequence alteration1nstd206human GRCh38 chr8: 66,567,052-67,159,532 , GRCh37.p13 chr8: 67,479,287-68,071,767 PTTG3P, MCMDC2, 15 more genes
    nsv5552462insertion1nstd206human GRCh38 chr8: 66,911,611-66,911,611 , GRCh37.p13 chr8: 67,823,846-67,823,846 MCMDC2
    nsv5484755copy number variation1nstd206human GRCh38 chr8: 66,902,127-66,902,207 , GRCh37.p13 chr8: 67,814,362-67,814,442 MCMDC2
    nsv5381480copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,786,376-68,165,857 , GRCh38.p12 chr8: 66,874,141-67,253,622 NPM1P44, LOC100288001, 10 more genes
    nsv4960730copy number variation1nstd200human GRCh38 chr8: 66,872,792-66,910,604 , GRCh37.p13 chr8: 67,785,027-67,822,839 MCMDC2
    nsv4765289insertion1nstd199human GRCh37 chr8: 67,814,363-67,814,363 , GRCh38.p12 chr8: 66,902,128-66,902,128 MCMDC2
    nsv4729605copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,744,375-68,387,850 , GRCh38.p12 chr8: 66,832,140-67,475,615 SNORD87, ARFGEF1-DT, 15 more genes
    nsv4729318copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,810,924-67,920,345 , GRCh38.p12 chr8: 66,898,689-67,008,110 MCMDC2, SNORD87, 4 more genes
    nsv4675786copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,718,713-68,020,835 , GRCh38.p12 chr8: 66,806,478-67,108,600 COPS5, SNHG6, 10 more genes
    nsv4675746copy number variation1nstd102humanLikely benign GRCh37 chr8: 67,828,205-68,074,172 , GRCh38.p12 chr8: 66,915,970-67,161,937 TCF24, COPS5, 8 more genes
    nsv4614315copy number variation1nstd183human GRCh37 chr8: 67,636,412-67,794,904 , GRCh38.p12 chr8: 66,724,177-66,882,669 SGK3, PTTG3P, 2 more genes
    nsv4613516copy number variation1nstd183human GRCh37 chr8: 67,792,828-67,793,361 , GRCh38.p12 chr8: 66,880,593-66,881,126 MCMDC2
    nsv4555972insertion1nstd166human GRCh37.p13 chr8: 67,814,341-67,814,341 , GRCh38.p12 chr8: 66,902,106-66,902,106 MCMDC2
    nsv4553962insertion1nstd166human GRCh37.p13 chr8: 67,814,362-67,814,362 , GRCh38.p12 chr8: 66,902,127-66,902,127 MCMDC2
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