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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935838copy number variation1nstd209human GRCh37.p13 chr20: 17,894,881-18,009,106 , GRCh38 chr20: 17,914,237-18,028,462 , PTMAP3, 4 more genes
    nsv5524167copy number variation1nstd206human GRCh38 chr20: 17,973,959-17,974,035 , GRCh37.p13 chr20: 17,954,602-17,954,678 MGME1
    nsv5328138copy number variation1nstd204human GRCh38.p13 chr20: 17,961,806-17,974,655 , GRCh37.p13 chr20: 17,942,449-17,955,298 SNX5, MGME1, 1 more genes
    nsv5297318copy number variation1nstd204human GRCh38.p13 chr20: 17,963,601-17,974,000 , GRCh37.p13 chr20: 17,944,244-17,954,643 SNX5, MGME1
    nsv5293360copy number variation1nstd204human GRCh38.p13 chr20: 17,962,551-17,974,633 , GRCh37.p13 chr20: 17,943,194-17,955,276 SNORD17, MGME1, 1 more genes
    nsv5290057copy number variation1nstd204human GRCh38.p13 chr20: 17,969,759-17,972,483 , GRCh37.p13 chr20: 17,950,402-17,953,126 MGME1
    nsv5286575copy number variation1nstd204human GRCh38.p13 chr20: 17,967,601-17,971,500 , GRCh37.p13 chr20: 17,948,244-17,952,143 SNX5, MGME1
    nsv5186217mobile element insertion1nstd203human GRCh38 chr20: 17,969,082-17,969,091 , GRCh37.p13 chr20: 17,949,725-17,949,734 SNX5, MGME1
    nsv5025177copy number variation1nstd200human GRCh38 chr20: 17,987,934-17,989,017 , GRCh37.p13 chr20: 17,968,577-17,969,660 MGME1
    nsv5025176copy number variation1nstd200human GRCh38 chr20: 17,962,291-17,974,238 , GRCh37.p13 chr20: 17,942,934-17,954,881 SNORD17, MGME1, 1 more genes
    nsv5021560copy number variation1nstd200human GRCh38 chr20: 17,976,287-17,978,395 , GRCh37.p13 chr20: 17,956,930-17,959,038 MGME1
    nsv5021559copy number variation1nstd200human GRCh38 chr20: 17,966,772-17,967,999 , GRCh37.p13 chr20: 17,947,415-17,948,642 SNX5, MGME1
    nsv4865467copy number variation1nstd200human GRCh37 chr20: 17,942,939-17,954,871 , GRCh38.p12 chr20: 17,962,296-17,974,228 MGME1, SNX5, 1 more genes
    nsv4865466copy number variation1nstd200human GRCh37 chr20: 17,894,827-18,009,130 , GRCh38.p12 chr20: 17,914,183-18,028,486 , MGME1, 4 more genes
    nsv4862223copy number variation1nstd200human GRCh37 chr20: 17,956,930-17,959,038 , GRCh38.p12 chr20: 17,976,287-17,978,395 MGME1
    nsv4862222copy number variation1nstd200human GRCh37 chr20: 17,956,885-17,957,376 , GRCh38.p12 chr20: 17,976,242-17,976,733 MGME1
    nsv4862221copy number variation1nstd200human GRCh37 chr20: 17,947,415-17,948,642 , GRCh38.p12 chr20: 17,966,772-17,967,999 SNX5, MGME1
    nsv4729849copy number variation1nstd102humanUncertain significance GRCh37 chr20: 17,845,611-18,089,764 , GRCh38.p12 chr20: 17,864,967-18,109,120 LOC105372548, PTMAP3, 7 more genes
    nsv4676419copy number variation1nstd102humanPathogenic GRCh37 chr20: 8,571,696-22,088,650 , GRCh38.p12 chr20: 8,591,049-22,108,012 PGAM3P, EEF1A1P34, 182 more genes
    nsv4627939copy number variation1nstd183human GRCh37 chr20: 17,943,618-17,951,057 , GRCh38.p12 chr20: 17,962,975-17,970,414 MGME1, SNX5, 1 more genes
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