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Items: 1 to 20 of 280

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5892369copy number variation1nstd209human GRCh38 chr6: 20,466,142-20,466,634 , GRCh37.p13 chr6: 20,466,373-20,466,865 E2F3
    nsv5888223copy number variation1nstd209human GRCh38 chr6: 20,419,596-20,419,897 , GRCh37.p13 chr6: 20,419,827-20,420,128 E2F3, RN7SL128P
    nsv5684199mobile element insertion1nstd211human GRCh38 chr6: 20,435,083-20,435,083 , GRCh37.p13 chr6: 20,435,314-20,435,314 E2F3
    nsv5553278insertion1nstd206human GRCh38 chr6: 20,467,910-20,467,914 , GRCh37.p13 chr6: 20,468,141-20,468,145 E2F3
    nsv5455987copy number variation1nstd206human GRCh38 chr6: 20,466,143-20,466,635 , GRCh37.p13 chr6: 20,466,374-20,466,866 E2F3
    nsv5455383copy number variation1nstd206human GRCh38 chr6: 20,463,725-20,466,452 , GRCh37.p13 chr6: 20,463,956-20,466,683 E2F3
    nsv5408834mobile element insertion1nstd206human GRCh38 chr6: 20,435,083-20,435,134 , GRCh37.p13 chr6: 20,435,314-20,435,365 E2F3
    nsv5378281translocation1nstd200human GRCh38 chr6: 20,440,977-20,440,977 , GRCh38 chr6: 20,440,918-20,440,918 , GRCh37.p13 chr6: 20,441,149-20,441,149 , GRCh37.p13 chr6: 20,441,208-20,441,208 E2F3
    nsv5378280translocation1nstd200human GRCh38 chr6: 20,431,215-20,431,215 , GRCh38 chr6: 20,431,139-20,431,139 , GRCh37.p13 chr6: 20,431,370-20,431,370 , GRCh37.p13 chr6: 20,431,446-20,431,446 E2F3
    nsv5378279translocation1nstd200human GRCh38 chr6: 20,408,432-20,408,432 , GRCh38 chr6: 20,408,329-20,408,329 , GRCh37.p13 chr6: 20,408,663-20,408,663 , GRCh37.p13 chr6: 20,408,560-20,408,560 E2F3
    nsv5303737copy number variation1nstd204human GRCh38.p13 chr6: 20,423,513-20,425,100 , GRCh37.p13 chr6: 20,423,744-20,425,331 E2F3
    nsv5098621mobile element insertion1nstd203human GRCh38 chr6: 20,445,472-20,445,505 , GRCh37.p13 chr6: 20,445,703-20,445,736 E2F3
    nsv5094229mobile element insertion1nstd203human GRCh38 chr6: 20,424,484-20,424,498 , GRCh37.p13 chr6: 20,424,715-20,424,729 E2F3
    nsv4934496copy number variation1nstd200human GRCh38 chr6: 20,489,899-20,490,157 , GRCh37.p13 chr6: 20,490,130-20,490,388 E2F3
    nsv4933055copy number variation1nstd200human GRCh38 chr6: 20,492,087-20,512,795 , GRCh37.p13 chr6: 20,492,318-20,513,026 E2F3
    nsv4933054copy number variation1nstd200human GRCh38 chr6: 20,483,295-20,484,619 , GRCh37.p13 chr6: 20,483,526-20,484,850 E2F3
    nsv4933053copy number variation1nstd200human GRCh38 chr6: 20,457,113-20,457,354 , GRCh37.p13 chr6: 20,457,344-20,457,585 E2F3
    nsv4933052copy number variation1nstd200human GRCh38 chr6: 20,444,425-20,444,548 , GRCh37.p13 chr6: 20,444,656-20,444,779 E2F3
    nsv4933051copy number variation1nstd200human GRCh38 chr6: 20,444,357-20,447,958 , GRCh37.p13 chr6: 20,444,588-20,448,189 E2F3
    nsv4933050copy number variation1nstd200human GRCh38 chr6: 20,423,539-20,425,077 , GRCh37.p13 chr6: 20,423,770-20,425,308 E2F3
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