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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121604copy number variation1nstd186human GRCh37 chr12: 110,099,111-110,100,069 , GRCh38.p12 chr12: 109,661,306-109,662,264 RN7SKP250
    nsv5942319copy number variation1nstd209human GRCh38 chr12: 109,662,520-109,662,756 , GRCh37.p13 chr12: 110,100,325-110,100,561 RN7SKP250
    nsv5938264copy number variation1nstd209human GRCh38 chr12: 109,662,084-109,662,173 , GRCh37.p13 chr12: 110,099,889-110,099,978 RN7SKP250
    nsv5933892copy number variation1nstd209human GRCh38 chr12: 109,661,694-109,661,968 , GRCh37.p13 chr12: 110,099,499-110,099,773 RN7SKP250
    nsv5928147copy number variation1nstd209human GRCh38 chr12: 109,661,944-109,662,213 , GRCh37.p13 chr12: 110,099,749-110,100,018 RN7SKP250
    nsv5657833insertion1nstd207human GRCh38 chr12: 109,662,136-109,662,136 , GRCh37.p13 chr12: 110,099,941-110,099,941 RN7SKP250
    nsv5653153insertion3nstd207human GRCh38 chr12: 109,661,596-109,661,596 , GRCh37.p13 chr12: 110,099,401-110,099,401 RN7SKP250
    nsv5652039insertion1nstd207human GRCh38 chr12: 109,661,579-109,661,579 , GRCh37.p13 chr12: 110,099,384-110,099,384 RN7SKP250
    nsv5649748insertion1nstd207human GRCh38 chr12: 109,662,025-109,662,025 , GRCh37.p13 chr12: 110,099,830-110,099,830 RN7SKP250
    nsv5646955insertion1nstd207human GRCh38 chr12: 109,661,666-109,661,666 , GRCh37.p13 chr12: 110,099,471-110,099,471 RN7SKP250
    nsv5644637insertion1nstd207human GRCh38 chr12: 109,661,833-109,661,833 , GRCh37.p13 chr12: 110,099,638-110,099,638 RN7SKP250
    nsv5540839insertion1nstd206human GRCh38 chr12: 109,661,493-109,661,507 , GRCh37.p13 chr12: 110,099,298-110,099,312 RN7SKP250
    nsv5507568copy number variation1nstd206human GRCh38 chr12: 109,661,945-109,662,091 , GRCh37.p13 chr12: 110,099,750-110,099,896 RN7SKP250
    nsv5506816copy number variation1nstd206human GRCh38 chr12: 109,662,520-109,662,750 , GRCh37.p13 chr12: 110,100,325-110,100,555 RN7SKP250
    nsv5499369copy number variation1nstd206human GRCh38 chr12: 109,661,042-109,662,349 , GRCh37.p13 chr12: 110,098,847-110,100,154 RN7SKP250
    nsv5390861copy number variation1nstd186human GRCh37 chr12: 110,099,068-110,099,898 , GRCh38.p12 chr12: 109,661,263-109,662,093 RN7SKP250
    nsv5390416copy number variation1nstd186human GRCh37 chr12: 110,099,067-110,100,098 , GRCh38.p12 chr12: 109,661,262-109,662,293 RN7SKP250
    nsv5389853copy number variation1nstd186human GRCh37 chr12: 110,100,325-110,100,580 , GRCh38.p12 chr12: 109,662,520-109,662,775 RN7SKP250
    nsv5316926copy number variation1nstd204human GRCh38.p13 chr12: 109,661,274-109,662,288 , GRCh37.p13 chr12: 110,099,079-110,100,093 RN7SKP250
    nsv5312011copy number variation1nstd204human GRCh38.p13 chr12: 109,662,271-109,662,578 , GRCh37.p13 chr12: 110,100,076-110,100,383 RN7SKP250
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