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Items: 1 to 20 of 213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5878507copy number variation1nstd209human GRCh38 chr2: 70,189,146-70,189,455 , GRCh37.p13 chr2: 70,416,278-70,416,587 C2orf42
    nsv5833792copy number variation1nstd209human GRCh38 chr2: 70,171,088-70,176,375 , GRCh37.p13 chr2: 70,398,220-70,403,507 C2orf42
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5537803insertion1nstd206human GRCh38 chr2: 70,176,501-70,176,541 , GRCh37.p13 chr2: 70,403,633-70,403,673 C2orf42
    nsv5446903copy number variation1nstd206human GRCh38 chr2: 70,190,121-70,190,196 , GRCh37.p13 chr2: 70,417,253-70,417,328 C2orf42
    nsv5442905copy number variation1nstd206human GRCh38 chr2: 70,157,309-70,159,375 , GRCh37.p13 chr2: 70,384,441-70,386,507 C2orf42
    nsv5442473copy number variation1nstd206human GRCh38 chr2: 70,187,394-70,188,257 , GRCh37.p13 chr2: 70,414,526-70,415,389 C2orf42
    nsv5212118mobile element deletion1nstd204human GRCh38.p13 chr2: 70,174,667-70,174,977 , GRCh37.p13 chr2: 70,401,799-70,402,109 C2orf42
    nsv5206418copy number variation1nstd204human GRCh38.p13 chr2: 70,058,501-70,325,800 , GRCh37.p13 chr2: 70,285,633-70,552,932 RN7SL470P, PCYOX1, 11 more genes
    nsv5064609mobile element insertion1nstd203human GRCh38 chr2: 70,164,317-70,164,331 , GRCh37.p13 chr2: 70,391,449-70,391,463 C2orf42
    nsv4908794copy number variation1nstd200human GRCh38 chr2: 70,159,550-70,194,136 , GRCh37.p13 chr2: 70,386,682-70,421,268 C2orf42
    nsv4901807copy number variation1nstd200human GRCh38 chr2: 70,170,030-70,173,500 , GRCh37.p13 chr2: 70,397,162-70,400,632 C2orf42
    nsv4901806copy number variation1nstd200human GRCh38 chr2: 70,155,006-70,157,183 , GRCh37.p13 chr2: 70,382,138-70,384,315 C2orf42
    nsv4872315mobile element deletion1nstd200human GRCh38 chr2: 70,174,676-70,174,969 , GRCh37.p13 chr2: 70,401,808-70,402,101 C2orf42
    nsv4786599mobile element deletion1nstd200human GRCh37 chr2: 70,401,808-70,402,101 , GRCh38.p12 chr2: 70,174,676-70,174,969 C2orf42
    nsv4776488copy number variation1nstd200human GRCh37 chr2: 70,382,138-70,384,315 , GRCh38.p12 chr2: 70,155,006-70,157,183 C2orf42
    nsv4659541copy number variation1nstd186human GRCh37 chr2: 70,384,386-70,386,540 , GRCh38.p12 chr2: 70,157,254-70,159,408 C2orf42
    nsv4586506copy number variation1nstd183human GRCh37 chr2: 70,384,386-70,386,540 , GRCh38.p12 chr2: 70,157,254-70,159,408 C2orf42
    nsv4518506copy number variation1nstd166human GRCh37.p13 chr2: 70,382,138-70,384,314 , GRCh38.p12 chr2: 70,155,006-70,157,182 C2orf42
    nsv4054264copy number variation1nstd166human GRCh37.p13 chr2: 70,356,719-70,385,862 , GRCh38.p12 chr2: 70,129,587-70,158,730 C2orf42
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