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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5970228inversion1nstd209human GRCh38 chr18: 42,666,448-47,133,105 , GRCh37.p13 chr18: 40,246,413-44,659,476 , ATP5F1A, 50 more genes
    nsv5939224copy number variation1nstd209human GRCh38 chr18: 45,832,259-45,832,432 , GRCh37.p13 chr18: 43,412,224-43,412,397 EPG5, SIGLEC15
    nsv5936878copy number variation1nstd209human GRCh38 chr18: 45,965,820-45,966,138 , GRCh37.p13 chr18: 43,545,786-43,546,104 EPG5
    nsv5935579copy number variation1nstd209human GRCh38 chr18: 45,951,467-45,951,549 , GRCh37.p13 chr18: 43,531,433-43,531,515 EPG5
    nsv5698207mobile element insertion1nstd211human GRCh38 chr18: 45,912,596-45,912,596 , GRCh37.p13 chr18: 43,492,561-43,492,561 EPG5
    nsv5661335insertion1nstd207human GRCh38 chr18: 45,956,736-45,956,736 , GRCh37.p13 chr18: 43,536,702-43,536,702 EPG5
    nsv5541605insertion1nstd206human GRCh38 chr18: 45,956,747-45,956,787 , GRCh37.p13 chr18: 43,536,713-43,536,753 EPG5
    nsv5533881copy number variation1nstd206human GRCh38 chr18: 45,940,557-45,940,648 , GRCh37.p13 chr18: 43,520,523-43,520,614 EPG5
    nsv5528881copy number variation1nstd206human GRCh38 chr18: 45,819,953-45,820,007 , GRCh37.p13 chr18: 43,399,918-43,399,972 EPG5
    nsv5526604copy number variation1nstd206human GRCh38 chr18: 45,830,884-45,831,978 , GRCh37.p13 chr18: 43,410,849-43,411,943 EPG5, SIGLEC15
    nsv5524469copy number variation1nstd206human GRCh38 chr18: 45,873,754-45,873,829 , GRCh37.p13 chr18: 43,453,719-43,453,794 EPG5
    nsv5519360copy number variation1nstd206human GRCh38 chr18: 45,815,434-45,846,165 , GRCh37.p13 chr18: 43,395,399-43,426,130 EPG5, SIGLEC15
    nsv5381046copy number variation2nstd102humanUncertain significance GRCh37 chr18: 42,281,312-45,423,127 , GRCh38.p12 chr18: 44,701,347-47,896,756 HDHD2, RNU6-1131P, 45 more genes
    nsv5329236copy number variation1nstd204human GRCh37.p13 chr18: 43,410,822-43,411,912 , GRCh38.p13 chr18: 45,830,857-45,831,947 SIGLEC15, EPG5
    nsv5157178mobile element insertion1nstd203human GRCh38 chr18: 45,912,578-45,912,593 , GRCh37.p13 chr18: 43,492,543-43,492,558 EPG5
    nsv5149934mobile element insertion1nstd203human GRCh38 chr18: 45,892,279-45,892,291 , GRCh37.p13 chr18: 43,472,244-43,472,256 EPG5
    nsv5024168copy number variation1nstd200human GRCh38 chr18: 45,843,821-45,854,639 , GRCh37.p13 chr18: 43,423,786-43,434,604 EPG5, SIGLEC15
    nsv5024167copy number variation1nstd200human GRCh38 chr18: 45,815,434-45,846,165 , GRCh37.p13 chr18: 43,395,399-43,426,130 SIGLEC15, EPG5
    nsv5024166copy number variation1nstd200human GRCh38 chr18: 45,784,855-45,839,490 , GRCh37.p13 chr18: 43,364,820-43,419,455 SIGLEC15, EPG5
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