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Items: 1 to 20 of 180

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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
    nsv5928275copy number variation1nstd209human GRCh38 chr16: 46,789,380-46,802,408 , GRCh37.p13 chr16: 46,823,292-46,836,320 C16orf87, LOC100130180
    nsv5870425copy number variation1nstd209human GRCh38 chr16: 46,798,387-46,800,886 , GRCh37.p13 chr16: 46,832,299-46,834,798 C16orf87
    nsv5868361copy number variation1nstd209human GRCh38 chr16: 46,789,522-46,800,661 , GRCh37.p13 chr16: 46,823,434-46,834,573 LOC100130180, C16orf87
    nsv5711769mobile element insertion1nstd211human GRCh38 chr16: 46,812,732-46,812,732 , GRCh37.p13 chr16: 46,846,644-46,846,644 C16orf87
    nsv5533554copy number variation1nstd206human GRCh38 chr16: 46,789,380-46,802,413 , GRCh37.p13 chr16: 46,823,292-46,836,325 C16orf87, LOC100130180
    nsv5522573copy number variation1nstd206human GRCh38 chr16: 46,386,400-46,898,682 , GRCh37.p13 chr16: 46,420,312-46,932,594 C16orf87, GPT2, 12 more genes
    nsv5426104mobile element insertion1nstd206human GRCh38 chr16: 46,812,732-46,812,783 , GRCh37.p13 chr16: 46,846,644-46,846,695 C16orf87
    nsv5320134copy number variation1nstd204human GRCh38.p13 chr16: 46,789,370-46,802,422 , GRCh37.p13 chr16: 46,823,282-46,836,334 LOC100130180, C16orf87
    nsv5267332copy number variation1nstd204human GRCh38.p13 chr16: 46,789,088-46,801,823 , GRCh37.p13 chr16: 46,823,000-46,835,735 C16orf87, LOC100130180
    nsv5005641copy number variation1nstd200human GRCh38 chr16: 46,789,380-46,802,413 , GRCh37.p13 chr16: 46,823,292-46,836,325 LOC100130180, C16orf87
    nsv4864135copy number variation1nstd200human GRCh37 chr16: 46,823,292-46,836,325 , GRCh38.p12 chr16: 46,789,380-46,802,413 LOC100130180, C16orf87
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4730011copy number variation1nstd102humanUncertain significance GRCh37 chr16: 46,503,572-47,114,342 , GRCh38.p12 chr16: 46,469,660-47,080,431 C16orf87, GPT2, 14 more genes
    nsv4729794copy number variation1nstd102humanUncertain significance GRCh37 chr16: 46,503,968-47,312,075 , GRCh38.p12 chr16: 46,470,056-47,278,164 LOC100130180, NETO2, 18 more genes
    nsv4675001copy number variation1nstd102humanUncertain significance GRCh37 chr16: 46,467,497-47,004,071 , GRCh38.p12 chr16: 46,433,585-46,970,159 LOC100130180, LOC441768, 13 more genes
    nsv4627972copy number variation1nstd183human GRCh37 chr16: 46,793,161-46,880,063 , GRCh38.p12 chr16: 46,759,249-46,846,151 MYLK3, CKBP1, 2 more genes
    nsv4625748copy number variation1nstd183human GRCh37 chr16: 46,858,137-46,916,594 , GRCh38.p12 chr16: 46,824,225-46,882,682 GPT2, CKBP1, 1 more genes
    nsv4429011copy number variation1nstd174human GRCh37 chr16: 46,463,770-46,874,684 , GRCh38.p12 chr16: 46,429,858-46,840,772 VPS35, SHCBP1, 9 more genes
    nsv4365843copy number variation1nstd173human GRCh37 chr16: 46,464,489-55,795,214 , GRCh38.p12 chr16: 46,430,577-55,761,302 , LOC100526838, 158 more genes
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