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Items: 1 to 20 of 243

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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
    nsv5979505inversion1nstd209human GRCh38 chr16: 46,982,903-47,949,086 , GRCh37.p13 chr16: 47,016,814-47,982,997 PHKB, ITFG1, 13 more genes
    nsv5979274insertion1nstd209human GRCh38 chr16: 47,115,716-47,115,716 , GRCh37.p13 chr16: 47,149,627-47,149,627 NETO2
    nsv5940157copy number variation1nstd209human GRCh38 chr16: 47,104,853-47,108,043 , GRCh37.p13 chr16: 47,138,764-47,141,954 NETO2
    nsv5875711copy number variation1nstd209human GRCh38 chr16: 47,104,726-47,107,475 , GRCh37.p13 chr16: 47,138,637-47,141,386 NETO2
    nsv5705038mobile element insertion2nstd211human GRCh38 chr16: 47,075,815-47,075,815 , GRCh37.p13 chr16: 47,109,726-47,109,726 NETO2
    nsv5702474mobile element insertion1nstd211human GRCh38 chr16: 47,090,605-47,090,605 , GRCh37.p13 chr16: 47,124,516-47,124,516 NETO2
    nsv5663781insertion2nstd207human GRCh38 chr16: 47,115,716-47,115,716 , GRCh37.p13 chr16: 47,149,627-47,149,627 NETO2
    nsv5540823insertion1nstd206human GRCh38 chr16: 47,108,205-47,108,247 , GRCh37.p13 chr16: 47,142,116-47,142,158 NETO2
    nsv5528971copy number variation1nstd206human GRCh38 chr16: 47,084,553-47,088,045 , GRCh37.p13 chr16: 47,118,464-47,121,956 NETO2
    nsv5520702copy number variation1nstd206human GRCh38 chr16: 47,112,695-47,113,792 , GRCh37.p13 chr16: 47,146,606-47,147,703 NETO2
    nsv5419972mobile element insertion1nstd206human GRCh38 chr16: 47,075,815-47,075,866 , GRCh37.p13 chr16: 47,109,726-47,109,777 NETO2
    nsv5358149translocation1nstd200human GRCh38 chr16: 47,073,851-47,073,851 , GRCh38 chr16: 47,075,720-47,075,720 , GRCh37.p13 chr16: 47,107,762-47,107,762 , GRCh37.p13 chr16: 47,109,631-47,109,631 NETO2
    nsv5333672translocation1nstd200human GRCh37 chr7: 20,709,861-20,709,861 , GRCh37 chr16: 47,114,609-47,114,609 , GRCh38.p12 chr16: 47,080,698-47,080,698 , GRCh38.p12 chr7: 20,670,238-20,670,238 NETO2, ABCB5
    nsv5183507mobile element insertion1nstd203human GRCh38 chr16: 47,080,683-47,080,699 , GRCh37.p13 chr16: 47,114,594-47,114,610 NETO2
    nsv5181751mobile element insertion1nstd203human GRCh38 chr16: 47,127,511-47,127,511 , GRCh37.p13 chr16: 47,161,422-47,161,422 NETO2
    nsv5153177mobile element insertion1nstd203human GRCh38 chr16: 47,077,636-47,077,651 , GRCh37.p13 chr16: 47,111,547-47,111,562 NETO2
    nsv5148175mobile element insertion1nstd203human GRCh38 chr16: 47,120,368-47,120,368 , GRCh37.p13 chr16: 47,154,279-47,154,279 NETO2
    nsv5146957mobile element insertion1nstd203human GRCh38 chr16: 47,095,133-47,095,146 , GRCh37.p13 chr16: 47,129,044-47,129,057 NETO2
    nsv5141284mobile element insertion1nstd203human GRCh38 chr16: 47,133,784-47,133,800 , GRCh37.p13 chr16: 47,167,695-47,167,711 NETO2
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