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Items: 1 to 20 of 184

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5883783copy number variation1nstd209human GRCh38 chr1: 35,022,539-35,022,998 , GRCh37.p13 chr1: 35,488,140-35,488,599 ZMYM6
    nsv5881202copy number variation1nstd209human GRCh38 chr1: 34,992,679-34,992,812 , GRCh37.p13 chr1: 35,458,280-35,458,413 ZMYM6
    nsv5693717mobile element insertion2nstd211human GRCh38 chr1: 34,998,640-34,998,640 , GRCh37.p13 chr1: 35,464,241-35,464,241 ZMYM6
    nsv5689901mobile element insertion1nstd211human GRCh38 chr1: 34,992,657-34,992,657 , GRCh37.p13 chr1: 35,458,258-35,458,258 ZMYM6
    nsv5678853mobile element insertion1nstd211human GRCh38 chr1: 35,029,475-35,029,475 , GRCh37.p13 chr1: 35,495,076-35,495,076 ZMYM6
    nsv5619003insertion1nstd207human GRCh38 chr1: 34,992,713-34,992,713 , GRCh37.p13 chr1: 35,458,314-35,458,314 ZMYM6
    nsv5617404insertion1nstd207human GRCh38 chr1: 35,015,743-35,015,743 , GRCh37.p13 chr1: 35,481,344-35,481,344 ZMYM6
    nsv5398791mobile element insertion1nstd206human GRCh38 chr1: 34,998,640-34,998,691 , GRCh37.p13 chr1: 35,464,241-35,464,292 ZMYM6
    nsv5361141translocation1nstd200human GRCh38 chr1: 35,022,542-35,022,542 , GRCh38 chr1: 35,022,999-35,022,999 , GRCh37.p13 chr1: 35,488,143-35,488,143 , GRCh37.p13 chr1: 35,488,600-35,488,600 ZMYM6
    nsv5338643translocation1nstd200human GRCh37 chr1: 35,488,143-35,488,143 , GRCh37 chr1: 35,488,600-35,488,600 , GRCh38.p12 chr1: 35,022,542-35,022,542 , GRCh38.p12 chr1: 35,022,999-35,022,999 ZMYM6
    nsv5296442copy number variation1nstd204human GRCh38.p13 chr1: 34,977,262-35,073,212 , GRCh37.p13 chr1: 35,442,863-35,538,813 ZMYM1, GPR199P, 3 more genes
    nsv5215408copy number variation1nstd204human GRCh38.p13 chr1: 34,977,101-35,073,200 , GRCh37.p13 chr1: 35,442,702-35,538,801 GPR199P, TMEM35B, 3 more genes
    nsv5212873copy number variation1nstd204human GRCh38.p13 chr1: 34,976,631-35,010,418 , GRCh37.p13 chr1: 35,442,232-35,476,019 ZMYM6, GPR199P, 1 more genes
    nsv5184106mobile element insertion1nstd203human GRCh38 chr1: 34,989,588-34,989,601 , GRCh37.p13 chr1: 35,455,189-35,455,202 ZMYM6
    nsv5075357mobile element insertion1nstd203human GRCh38 chr1: 34,998,624-34,998,640 , GRCh37.p13 chr1: 35,464,225-35,464,241 ZMYM6
    nsv4903346copy number variation1nstd200human GRCh38 chr1: 34,993,160-34,993,908 , GRCh37.p13 chr1: 35,458,761-35,459,509 ZMYM6
    nsv4895921copy number variation1nstd200human GRCh38 chr1: 35,024,621-35,036,435 , GRCh37.p13 chr1: 35,490,222-35,502,036 ZMYM6
    nsv4895920copy number variation1nstd200human GRCh38 chr1: 35,023,812-35,026,105 , GRCh37.p13 chr1: 35,489,413-35,491,706 ZMYM6
    nsv4895919copy number variation1nstd200human GRCh38 chr1: 34,993,110-35,001,471 , GRCh37.p13 chr1: 35,458,711-35,467,072 ZMYM6
    nsv4780772copy number variation1nstd200human GRCh37 chr1: 35,450,344-35,461,383 , GRCh38.p12 chr1: 34,984,743-34,995,782 TMEM35B, ZMYM6
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