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Items: 1 to 20 of 690

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958342insertion1nstd209human GRCh38 chr2: 62,095,807-62,095,807 , GRCh37.p13 chr2: 62,322,942-62,322,942 , COMMD1
    nsv5878547copy number variation1nstd209human GRCh38 chr2: 61,904,073-61,907,167 , GRCh37.p13 chr2: 62,131,208-62,134,302 COMMD1
    nsv5878337copy number variation1nstd209human GRCh38 chr2: 62,123,224-62,124,017 , GRCh37.p13 chr2: 62,350,359-62,351,152 COMMD1
    nsv5876341copy number variation1nstd209human GRCh38 chr2: 61,892,586-61,893,570 , GRCh37.p13 chr2: 62,119,721-62,120,705 COMMD1
    nsv5876175copy number variation1nstd209human GRCh38 chr2: 62,077,622-62,077,695 , GRCh37.p13 chr2: 62,304,757-62,304,830 COMMD1
    nsv5869334copy number variation1nstd209human GRCh38 chr2: 62,127,815-62,154,615 , GRCh37.p13 chr2: 62,354,950-62,381,750 RPSAP26, COMMD1
    nsv5833997copy number variation1nstd209human GRCh38 chr2: 62,130,570-62,148,727 , GRCh37.p13 chr2: 62,357,705-62,375,862 COMMD1, RPSAP26
    nsv5833678copy number variation1nstd209human GRCh38 chr2: 61,972,198-61,973,297 , GRCh37.p13 chr2: 62,199,333-62,200,432 COMMD1
    nsv5833084copy number variation1nstd209human GRCh38 chr2: 61,904,040-61,907,189 , GRCh37.p13 chr2: 62,131,175-62,134,324 COMMD1
    nsv5720305mobile element insertion2nstd211human GRCh38 chr2: 61,965,831-61,965,831 , GRCh37.p13 chr2: 62,192,966-62,192,966 COMMD1
    nsv5685253mobile element insertion1nstd211human GRCh38 chr2: 61,975,140-61,975,140 , GRCh37.p13 chr2: 62,202,275-62,202,275 COMMD1
    nsv5682407mobile element insertion2nstd211human GRCh38 chr2: 62,108,744-62,108,744 , GRCh37.p13 chr2: 62,335,879-62,335,879 COMMD1
    nsv5681508mobile element insertion1nstd211human GRCh38 chr2: 61,895,250-61,895,250 , GRCh37.p13 chr2: 62,122,385-62,122,385 COMMD1
    nsv5620402insertion1nstd207human GRCh38 chr2: 61,967,510-61,967,510 , GRCh37.p13 chr2: 62,194,645-62,194,645 COMMD1
    nsv5608468insertion1nstd207human GRCh38 chr2: 61,963,267-61,963,267 , GRCh37.p13 chr2: 62,190,402-62,190,402 COMMD1
    nsv5559155mobile element insertion1nstd206human GRCh38 chr2: 61,965,831-61,965,882 , GRCh37.p13 chr2: 62,192,966-62,193,017 COMMD1
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5453700copy number variation1nstd206human GRCh38 chr2: 62,045,789-62,048,265 , GRCh37.p13 chr2: 62,272,924-62,275,400 COMMD1
    nsv5453566copy number variation1nstd206human GRCh38 chr2: 61,889,500-61,893,122 , GRCh37.p13 chr2: 62,116,635-62,120,257 COMMD1
    nsv5452299copy number variation1nstd206human GRCh38 chr2: 61,968,609-62,004,549 , GRCh37.p13 chr2: 62,195,744-62,231,684 COMMD1
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