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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673923copy number variation1nstd102humanPathogenic GRCh37 chr6: 72,596,727-74,363,609 , GRCh38.p12 chr6: 71,887,024-73,653,886 LOC100422453, RPS27P15, 32 more genes
    nsv5457340copy number variation1nstd206human GRCh38 chr6: 73,408,675-73,418,543 , GRCh37.p13 chr6: 74,118,398-74,128,266 DDX43
    nsv5232363copy number variation1nstd204human GRCh38.p13 chr6: 73,323,901-73,711,800 , GRCh37.p13 chr6: 74,033,624-74,421,523 OOEP, RN7SL827P, 15 more genes
    nsv5109844mobile element insertion1nstd203human GRCh38 chr6: 73,417,457-73,417,474 , GRCh37.p13 chr6: 74,127,180-74,127,197 DDX43
    nsv5033711inversion1nstd200human GRCh38 chr6: 66,790,667-77,039,639 , GRCh37.p13 chr6: 67,500,560-77,749,356 , FAM135A-AS1, 116 more genes
    nsv4933599copy number variation1nstd200human GRCh38 chr6: 73,414,311-73,414,454 , GRCh37.p13 chr6: 74,124,034-74,124,177 DDX43
    nsv4933598copy number variation1nstd200human GRCh38 chr6: 73,408,698-73,418,519 , GRCh37.p13 chr6: 74,118,421-74,128,242 DDX43
    nsv4933597copy number variation1nstd200human GRCh38 chr6: 73,403,221-73,403,446 , GRCh37.p13 chr6: 74,112,944-74,113,169 DDX43
    nsv4810423copy number variation1nstd200human GRCh37 chr6: 74,124,034-74,124,177 , GRCh38.p12 chr6: 73,414,311-73,414,454 DDX43
    nsv4810422copy number variation1nstd200human GRCh37 chr6: 74,118,421-74,128,242 , GRCh38.p12 chr6: 73,408,698-73,418,519 DDX43
    nsv4778643mobile element deletion1nstd200human GRCh37 chr6: 74,118,278-74,118,578 , GRCh38.p12 chr6: 73,408,555-73,408,855 DDX43
    nsv4680743copy number variation1nstd189human GRCh37.p13 chr6: 73,919,920-74,316,780 , GRCh38.p12 chr6: 73,210,197-73,607,057 , EEF1A1, 18 more genes
    nsv4675253copy number variation1nstd102humanUncertain significance GRCh37 chr6: 73,881,985-74,138,519 , GRCh38.p12 chr6: 73,172,262-73,428,796 KCNQ5, OOEP, 13 more genes
    nsv4608447copy number variation1nstd183human GRCh37 chr6: 74,126,941-74,182,222 , GRCh38.p12 chr6: 73,417,218-73,472,499 MTO1, CGAS, 2 more genes
    nsv4608263copy number variation1nstd183human GRCh37 chr6: 74,117,281-74,117,487 , GRCh38.p12 chr6: 73,407,558-73,407,764 DDX43
    nsv4491606mobile element insertion1nstd166human GRCh37.p13 chr6: 74,127,180-74,127,180 , GRCh38.p12 chr6: 73,417,457-73,417,457 DDX43
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv4144593copy number variation1nstd166human GRCh37.p13 chr6: 73,936,058-74,735,891 , GRCh38.p12 chr6: 73,226,335-74,026,175 , DDX43, 20 more genes
    nsv4139698copy number variation1nstd166human GRCh37.p13 chr6: 74,112,944-74,113,169 , GRCh38.p12 chr6: 73,403,221-73,403,446 DDX43
    nsv3924180copy number variation1nstd102humanPathogenic NCBI36 chr6: 65,316,269-84,193,229 , GRCh38 chr6: 64,549,655-83,426,791 , GRCh37 chr6: 65,259,548-84,136,510 LOC105377875, KCNQ5-IT1, 188 more genes
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