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Items: 1 to 20 of 284

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5723746mobile element insertion1nstd211human GRCh38 chr1: 119,040,364-119,040,364 , GRCh37.p13 chr1: 119,582,987-119,582,987 WARS2
    nsv5715934mobile element insertion2nstd211human GRCh38 chr1: 119,072,160-119,072,160 , GRCh37.p13 chr1: 119,614,783-119,614,783 WARS2
    nsv5692720mobile element insertion1nstd211human GRCh38 chr1: 119,103,823-119,103,823 , GRCh37.p13 chr1: 119,646,446-119,646,446 WARS2
    nsv5680789mobile element insertion2nstd211human GRCh38 chr1: 119,064,880-119,064,880 , GRCh37.p13 chr1: 119,607,503-119,607,503 WARS2
    nsv5563217mobile element insertion1nstd206human GRCh38 chr1: 119,040,364-119,040,415 , GRCh37.p13 chr1: 119,582,987-119,583,038 WARS2
    nsv5407129mobile element insertion1nstd206human GRCh38 chr1: 119,064,880-119,064,931 , GRCh37.p13 chr1: 119,607,503-119,607,554 WARS2
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 AMYP1, MIR4256, 320 more genes
    nsv5218115copy number variation1nstd204human GRCh38.p13 chr1: 119,106,801-119,110,900 , GRCh37.p13 chr1: 119,649,424-119,653,523 WARS2
    nsv5201334copy number variation1nstd204human GRCh38.p13 chr1: 119,058,401-119,058,800 , GRCh37.p13 chr1: 119,601,024-119,601,423 WARS2-IT1, WARS2
    nsv5071641mobile element insertion1nstd203human GRCh38 chr1: 119,064,868-119,064,880 , GRCh37.p13 chr1: 119,607,491-119,607,503 WARS2
    nsv5060720mobile element insertion1nstd203human GRCh38 chr1: 119,064,872-119,064,880 , GRCh37.p13 chr1: 119,607,495-119,607,503 WARS2
    nsv4891010copy number variation1nstd200human GRCh38 chr1: 119,132,234-119,200,134 , GRCh37.p13 chr1: 119,674,857-119,742,757 WARS2-AS1, WARS2
    nsv4891009copy number variation1nstd200human GRCh38 chr1: 119,109,773-119,114,033 , GRCh37.p13 chr1: 119,652,396-119,656,656 WARS2
    nsv4891008copy number variation1nstd200human GRCh38 chr1: 119,074,763-119,076,273 , GRCh37.p13 chr1: 119,617,386-119,618,896 WARS2
    nsv4891007copy number variation1nstd200human GRCh38 chr1: 119,071,578-119,073,287 , GRCh37.p13 chr1: 119,614,201-119,615,910 WARS2
    nsv4891006copy number variation1nstd200human GRCh38 chr1: 119,065,024-119,069,875 , GRCh37.p13 chr1: 119,607,647-119,612,498 WARS2
    nsv4891005copy number variation1nstd200human GRCh38 chr1: 119,029,117-119,030,932 , GRCh37.p13 chr1: 119,571,740-119,573,555 WARS2
    nsv4773860copy number variation1nstd200human GRCh37 chr1: 119,652,396-119,656,656 , GRCh38.p12 chr1: 119,109,773-119,114,033 WARS2
    nsv4773859copy number variation1nstd200human GRCh37 chr1: 119,617,386-119,618,896 , GRCh38.p12 chr1: 119,074,763-119,076,273 WARS2
    nsv4773858copy number variation1nstd200human GRCh37 chr1: 119,598,616-119,605,727 , GRCh38.p12 chr1: 119,055,993-119,063,104 WARS2-IT1, WARS2
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