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Items: 1 to 20 of 208

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5689805mobile element insertion2nstd211human GRCh38 chr3: 94,124,591-94,124,591 , GRCh37.p13 chr3: 93,843,435-93,843,435 NSUN3
    nsv5685687mobile element insertion1nstd211human GRCh38 chr3: 94,117,864-94,117,864 , GRCh37.p13 chr3: 93,836,708-93,836,708 NSUN3
    nsv5448245copy number variation1nstd206human GRCh38 chr3: 94,093,403-94,096,881 , GRCh37.p13 chr3: 93,812,247-93,815,725 NSUN3
    nsv5443615copy number variation1nstd206human GRCh38 chr3: 94,089,653-94,089,751 , GRCh37.p13 chr3: 93,808,497-93,808,595 NSUN3
    nsv5442929copy number variation1nstd206human GRCh38 chr3: 94,083,487-94,086,604 , GRCh37.p13 chr3: 93,802,331-93,805,448 NSUN3
    nsv5435306copy number variation1nstd206human GRCh38 chr3: 94,089,686-94,096,879 , GRCh37.p13 chr3: 93,808,530-93,815,723 NSUN3
    nsv5406414mobile element insertion1nstd206human GRCh38 chr3: 94,117,864-94,117,915 , GRCh37.p13 chr3: 93,836,708-93,836,759 NSUN3
    nsv5396173mobile element insertion1nstd206human GRCh38 chr3: 94,124,591-94,124,642 , GRCh37.p13 chr3: 93,843,435-93,843,486 NSUN3
    nsv5346259translocation1nstd200human GRCh38 chr3: 94,097,116-94,097,116 , GRCh38 chr3: 94,097,613-94,097,613 , GRCh37.p13 chr3: 93,815,960-93,815,960 , GRCh37.p13 chr3: 93,816,457-93,816,457 NSUN3
    nsv5313998copy number variation1nstd204human GRCh38.p13 chr3: 94,083,477-94,086,613 , GRCh37.p13 chr3: 93,802,321-93,805,457 NSUN3
    nsv5230607copy number variation1nstd204human GRCh38.p13 chr3: 94,084,305-94,087,104 , GRCh37.p13 chr3: 93,803,149-93,805,948 NSUN3
    nsv5088750mobile element insertion1nstd203human GRCh38 chr3: 94,124,577-94,124,586 , GRCh37.p13 chr3: 93,843,421-93,843,430 NSUN3
    nsv4914508copy number variation1nstd200human GRCh38 chr3: 94,062,846-94,063,013 , GRCh37.p13 chr3: 93,781,690-93,781,857 DHFR2, NSUN3
    nsv4914506copy number variation1nstd200human GRCh38 chr3: 93,991,806-94,228,578 , GRCh37.p13 chr3: 93,710,650-93,947,422 DHFR2, RBBP4P2, 3 more genes
    nsv4911983copy number variation1nstd200human GRCh38 chr3: 94,093,413-94,096,879 , GRCh37.p13 chr3: 93,812,257-93,815,723 NSUN3
    nsv4911982copy number variation1nstd200human GRCh38 chr3: 94,089,685-94,096,879 , GRCh37.p13 chr3: 93,808,529-93,815,723 NSUN3
    nsv4911981copy number variation1nstd200human GRCh38 chr3: 94,089,686-94,093,348 , GRCh37.p13 chr3: 93,808,530-93,812,192 NSUN3
    nsv4911980copy number variation1nstd200human GRCh38 chr3: 94,083,487-94,086,604 , GRCh37.p13 chr3: 93,802,331-93,805,448 NSUN3
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4755509insertion1nstd199human GRCh37 chr3: 93,829,101-93,829,101 , GRCh38.p12 chr3: 94,110,257-94,110,257 NSUN3
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