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Items: 1 to 20 of 534

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5956597insertion1nstd209human GRCh38 chr7: 135,452,280-135,452,280 , GRCh37.p13 chr7: 135,137,028-135,137,028 CNOT4
    nsv5921721copy number variation1nstd209human GRCh38 chr7: 135,446,905-135,447,214 , GRCh37.p13 chr7: 135,131,653-135,131,962 CNOT4
    nsv5918895copy number variation1nstd209human GRCh38 chr7: 135,494,208-135,495,242 , GRCh37.p13 chr7: 135,178,956-135,179,990 CNOT4
    nsv5908197copy number variation1nstd209human GRCh38 chr7: 135,456,282-135,459,310 , GRCh37.p13 chr7: 135,141,030-135,144,058 CNOT4
    nsv5851578copy number variation1nstd209human GRCh38 chr7: 135,456,374-135,459,326 , GRCh37.p13 chr7: 135,141,122-135,144,074 CNOT4
    nsv5847737copy number variation1nstd209human GRCh38 chr7: 135,470,016-135,473,472 , GRCh37.p13 chr7: 135,154,764-135,158,220 CNOT4
    nsv5725704mobile element insertion1nstd211human GRCh38 chr7: 135,488,546-135,488,546 , GRCh37.p13 chr7: 135,173,294-135,173,294 CNOT4
    nsv5715374mobile element insertion1nstd211human GRCh38 chr7: 135,488,531-135,488,531 , GRCh37.p13 chr7: 135,173,279-135,173,279 CNOT4
    nsv5714467mobile element insertion1nstd211human GRCh38 chr7: 135,382,523-135,382,523 , GRCh37.p13 chr7: 135,067,275-135,067,275 CNOT4
    nsv5708260mobile element insertion2nstd211human GRCh38 chr7: 135,472,515-135,472,515 , GRCh37.p13 chr7: 135,157,263-135,157,263 CNOT4
    nsv5707660mobile element insertion1nstd211human GRCh38 chr7: 135,464,040-135,464,040 , GRCh37.p13 chr7: 135,148,788-135,148,788 CNOT4
    nsv5700979mobile element insertion1nstd211human GRCh38 chr7: 135,383,901-135,383,901 , GRCh37.p13 chr7: 135,068,653-135,068,653 CNOT4
    nsv5695235mobile element insertion2nstd211human GRCh38 chr7: 135,386,580-135,386,580 , GRCh37.p13 chr7: 135,071,332-135,071,332 CNOT4
    nsv5633177insertion1nstd207human GRCh38 chr7: 135,452,280-135,452,280 , GRCh37.p13 chr7: 135,137,028-135,137,028 CNOT4
    nsv5580886copy number variation1nstd207human GRCh38 chr7: 135,504,451-135,504,784 , GRCh37.p13 chr7: 135,189,199-135,189,532 CNOT4
    nsv5577268copy number variation1nstd207human GRCh38 chr7: 135,446,905-135,447,214 , GRCh37.p13 chr7: 135,131,653-135,131,962 CNOT4
    nsv5568258copy number variation1nstd207human GRCh38 chr7: 135,495,686-135,495,737 , GRCh37.p13 chr7: 135,180,434-135,180,485 CNOT4
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5547258insertion1nstd206human GRCh38 chr7: 135,452,298-135,452,322 , GRCh37.p13 chr7: 135,137,046-135,137,070 CNOT4
    nsv5485439copy number variation1nstd206human GRCh38 chr7: 135,446,905-135,447,215 , GRCh37.p13 chr7: 135,131,653-135,131,963 CNOT4
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