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Items: 1 to 20 of 295

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980275insertion1nstd209human GRCh38 chr11: 95,896,229-95,896,229 , GRCh37.p13 chr11: 95,629,393-95,629,393 MTMR2
    nsv5975161insertion1nstd209human GRCh38 chr11: 95,850,217-95,850,217 , GRCh37.p13 chr11: 95,583,381-95,583,381 MTMR2
    nsv5923225copy number variation1nstd209human GRCh38 chr11: 95,849,517-95,849,623 , GRCh37.p13 chr11: 95,582,681-95,582,787 MTMR2
    nsv5921606copy number variation1nstd209human GRCh38 chr11: 95,847,898-95,849,671 , GRCh37.p13 chr11: 95,581,062-95,582,835 MTMR2
    nsv5916987copy number variation1nstd209human GRCh38 chr11: 95,845,159-95,847,712 , GRCh37.p13 chr11: 95,578,323-95,580,876 MTMR2
    nsv5912599copy number variation1nstd209human GRCh38 chr11: 95,835,450-95,836,145 , GRCh37.p13 chr11: 95,568,614-95,569,309 MTMR2
    nsv5910093copy number variation1nstd209human GRCh38 chr11: 95,839,873-95,839,927 , GRCh37.p13 chr11: 95,573,037-95,573,091 MTMR2, RNA5SP345
    nsv5908282copy number variation1nstd209human GRCh38 chr11: 95,836,324-95,838,092 , GRCh37.p13 chr11: 95,569,488-95,571,256 RNA5SP345, MTMR2
    nsv5725275mobile element insertion1nstd211human GRCh38 chr11: 95,918,151-95,918,151 , GRCh37.p13 chr11: 95,651,315-95,651,315 MTMR2
    nsv5709358mobile element insertion2nstd211human GRCh38 chr11: 95,853,675-95,853,675 , GRCh37.p13 chr11: 95,586,839-95,586,839 MTMR2
    nsv5708512mobile element insertion2nstd211human GRCh38 chr11: 95,917,014-95,917,014 , GRCh37.p13 chr11: 95,650,178-95,650,178 MTMR2
    nsv5701546mobile element insertion1nstd211human GRCh38 chr11: 95,901,857-95,901,857 , GRCh37.p13 chr11: 95,635,021-95,635,021 MTMR2
    nsv5695834mobile element insertion2nstd211human GRCh38 chr11: 95,907,938-95,907,938 , GRCh37.p13 chr11: 95,641,102-95,641,102 MTMR2
    nsv5695098mobile element insertion2nstd211human GRCh38 chr11: 95,850,233-95,850,233 , GRCh37.p13 chr11: 95,583,397-95,583,397 MTMR2
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5654908insertion1nstd207human GRCh38 chr11: 95,850,217-95,850,217 , GRCh37.p13 chr11: 95,583,381-95,583,381 MTMR2
    nsv5551624insertion1nstd206human GRCh38 chr11: 95,920,569-95,920,620 , GRCh37.p13 chr11: 95,653,733-95,653,784 MTMR2
    nsv5513371copy number variation1nstd206human GRCh38 chr11: 95,845,032-95,847,713 , GRCh37.p13 chr11: 95,578,196-95,580,877 MTMR2
    nsv5512920copy number variation1nstd206human GRCh38 chr11: 95,835,454-95,836,146 , GRCh37.p13 chr11: 95,568,618-95,569,310 MTMR2
    nsv5511388copy number variation1nstd206human GRCh38 chr11: 95,865,253-95,865,320 , GRCh37.p13 chr11: 95,598,417-95,598,484 MTMR2
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