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Items: 1 to 20 of 231

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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
    nsv5936563copy number variation1nstd209human GRCh38 chr16: 46,750,571-46,750,869 , GRCh37.p13 chr16: 46,784,483-46,784,781 MYLK3
    nsv5728726mobile element insertion1nstd211human GRCh38 chr16: 46,724,173-46,724,173 , GRCh37.p13 chr16: 46,758,085-46,758,085 MYLK3
    nsv5701374mobile element insertion1nstd211human GRCh38 chr16: 46,702,974-46,702,974 , GRCh37.p13 chr16: 46,736,886-46,736,886 MYLK3
    nsv5697202mobile element insertion2nstd211human GRCh38 chr16: 46,701,070-46,701,070 , GRCh37.p13 chr16: 46,734,982-46,734,982 MYLK3
    nsv5554671mobile element insertion1nstd206human GRCh38 chr16: 46,724,184-46,724,193 , GRCh37.p13 chr16: 46,758,096-46,758,105 MYLK3
    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
    nsv5428245mobile element insertion1nstd206human GRCh38 chr16: 46,701,070-46,701,121 , GRCh37.p13 chr16: 46,734,982-46,735,033 MYLK3
    nsv5317096copy number variation1nstd204human GRCh38.p13 chr16: 46,719,223-46,720,037 , GRCh37.p13 chr16: 46,753,135-46,753,949 MYLK3
    nsv5146732mobile element insertion1nstd203human GRCh38 chr16: 46,706,598-46,706,609 , GRCh37.p13 chr16: 46,740,510-46,740,521 MYLK3
    nsv5140853mobile element insertion1nstd203human GRCh38 chr16: 46,706,597-46,706,609 , GRCh37.p13 chr16: 46,740,509-46,740,521 MYLK3
    nsv5003956copy number variation1nstd200human GRCh38 chr16: 46,761,910-46,762,065 , GRCh37.p13 chr16: 46,795,822-46,795,977 MYLK3
    nsv4856969copy number variation1nstd200human GRCh37 chr16: 46,753,110-46,753,923 , GRCh38.p12 chr16: 46,719,198-46,720,011 MYLK3
    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
    nsv4513513mobile element insertion1nstd166human GRCh37.p13 chr16: 46,740,510-46,740,510 , GRCh38.p12 chr16: 46,706,598-46,706,598 MYLK3
    nsv4505158mobile element insertion1nstd166human GRCh37.p13 chr16: 46,734,972-46,734,972 , GRCh38.p12 chr16: 46,701,060-46,701,060 MYLK3
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