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Items: 1 to 20 of 194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5664043insertion1nstd207human GRCh38 chr16: 50,563,848-50,563,848 , GRCh37.p13 chr16: 50,597,759-50,597,759 NKD1
    nsv5654384insertion1nstd207human GRCh38 chr16: 50,563,549-50,563,549 , GRCh37.p13 chr16: 50,597,460-50,597,460 NKD1
    nsv5601956copy number variation1nstd207human GRCh38 chr16: 50,563,365-50,563,604 , GRCh37.p13 chr16: 50,597,276-50,597,515 NKD1
    nsv5591831copy number variation1nstd207human GRCh38 chr16: 50,579,427-50,579,540 , GRCh37.p13 chr16: 50,613,338-50,613,451 NKD1
    nsv5589094copy number variation1nstd207human GRCh38 chr16: 50,563,788-50,563,847 , GRCh37.p13 chr16: 50,597,699-50,597,758 NKD1
    nsv5358178translocation1nstd200human GRCh38 chr16: 50,596,521-50,596,521 , GRCh38 chr16: 50,593,613-50,593,613 , GRCh37.p13 chr16: 50,627,524-50,627,524 , GRCh37.p13 chr16: 50,630,432-50,630,432 NKD1
    nsv5004080copy number variation1nstd200human GRCh38 chr16: 50,578,327-50,590,177 , GRCh37.p13 chr16: 50,612,238-50,624,088 NKD1
    nsv5004079copy number variation1nstd200human GRCh38 chr16: 50,573,648-50,574,694 , GRCh37.p13 chr16: 50,607,559-50,608,605 NKD1
    nsv4857080copy number variation1nstd200human GRCh37 chr16: 50,612,238-50,624,088 , GRCh38.p12 chr16: 50,578,327-50,590,177 NKD1
    nsv4857079copy number variation1nstd200human GRCh37 chr16: 50,607,559-50,608,605 , GRCh38.p12 chr16: 50,573,648-50,574,694 NKD1
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4747992copy number variation1nstd199human GRCh37 chr16: 50,597,786-50,597,844 , GRCh38.p12 chr16: 50,563,875-50,563,933 NKD1
    nsv4746752copy number variation1nstd199human GRCh37 chr16: 50,623,598-50,623,654 , GRCh38.p12 chr16: 50,589,687-50,589,743 NKD1
    nsv4743426copy number variation1nstd199human GRCh37 chr16: 50,613,309-50,613,426 , GRCh38.p12 chr16: 50,579,398-50,579,515 NKD1
    nsv4702776copy number variation1nstd195human GRCh37 chr16: 50,383,251-51,282,851 , GRCh38.p12 chr16: 50,349,340-51,248,940 , BRD7, 18 more genes
    nsv4666064copy number variation1nstd186human GRCh37 chr16: 50,582,449-50,582,499 , GRCh38.p12 chr16: 50,548,538-50,548,588 NKD1
    nsv4623964copy number variation2nstd183human GRCh37 chr16: 50,582,449-50,582,499 , GRCh38.p12 chr16: 50,548,538-50,548,588 NKD1
    nsv4365843copy number variation1nstd173human GRCh37 chr16: 46,464,489-55,795,214 , GRCh38.p12 chr16: 46,430,577-55,761,302 , LOC100526838, 158 more genes
    nsv4365186copy number variation1nstd173human GRCh37 chr16: 46,503,205-57,376,253 , GRCh38.p12 chr16: 46,469,293-57,342,341 , TOX3, 210 more genes
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