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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960840insertion1nstd209human GRCh38 chr9: 34,492,497-34,492,497 , GRCh37.p13 chr9: 34,492,495-34,492,495 DNAI1
    nsv5920151copy number variation1nstd209human GRCh38 chr9: 34,518,759-34,518,928 , GRCh37.p13 chr9: 34,518,757-34,518,926 DNAI1
    nsv5917526copy number variation1nstd209human GRCh38 chr9: 34,482,243-34,482,640 , GRCh37.p13 chr9: 34,482,241-34,482,638 DNAI1
    nsv5708765mobile element insertion1nstd211human GRCh38 chr9: 34,479,387-34,479,387 , GRCh37.p13 chr9: 34,479,385-34,479,385 RN7SKP24, DNAI1
    nsv5674172copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 34,489,311-34,493,336 , GRCh38.p12 chr9: 34,489,313-34,493,338 DNAI1
    nsv5674074copy number variation1nstd102humanPathogenic GRCh37 chr9: 34,459,004-36,276,941 , GRCh38.p12 chr9: 34,459,006-36,276,944 SPAG8, DNAI1, 84 more genes
    nsv5673891copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 34,489,311-34,520,764 , GRCh38.p12 chr9: 34,489,313-34,520,766 DNAI1, ENHO
    nsv5405263mobile element insertion1nstd206human GRCh38 chr9: 34,479,387-34,479,438 , GRCh37.p13 chr9: 34,479,385-34,479,436 RN7SKP24, DNAI1
    nsv5381707copy number variation2nstd102humanUncertain significance GRCh37 chr9: 34,458,994-35,072,710 , GRCh38.p12 chr9: 34,458,996-35,072,713 YWHAZP6, IL11RA, 30 more genes
    nsv5317627copy number variation1nstd204human GRCh37.p13 chr9: 34,516,307-34,519,774 , GRCh38.p13 chr9: 34,516,309-34,519,776 DNAI1, ENHO
    nsv5316440copy number variation1nstd204human GRCh38.p13 chr9: 34,473,338-34,475,028 , GRCh37.p13 chr9: 34,473,336-34,475,026 DNAI1
    nsv5256518copy number variation1nstd204human GRCh38.p13 chr9: 34,500,201-34,504,900 , GRCh37.p13 chr9: 34,500,199-34,504,898 DNAI1
    nsv5245496copy number variation1nstd204human GRCh38.p13 chr9: 34,516,317-34,519,754 , GRCh37.p13 chr9: 34,516,315-34,519,752 ENHO, DNAI1
    nsv5133528mobile element insertion1nstd203human GRCh38 chr9: 34,479,373-34,479,387 , GRCh37.p13 chr9: 34,479,371-34,479,385 RN7SKP24, DNAI1
    nsv4964279copy number variation1nstd200human GRCh38 chr9: 34,474,793-34,477,226 , GRCh37.p13 chr9: 34,474,791-34,477,224 RN7SKP24, DNAI1
    nsv4954657copy number variation1nstd200human GRCh38 chr9: 34,103,197-34,805,619 , GRCh37.p13 chr9: 34,103,195-34,805,616 , CCL27, 32 more genes
    nsv4828246copy number variation1nstd200human GRCh37 chr9: 34,516,329-34,519,746 , GRCh38.p12 chr9: 34,516,331-34,519,748 DNAI1, ENHO
    nsv4828245copy number variation1nstd200human GRCh37 chr9: 34,482,134-34,482,589 , GRCh38.p12 chr9: 34,482,136-34,482,591 DNAI1
    nsv4828244copy number variation1nstd200human GRCh37 chr9: 34,474,791-34,477,224 , GRCh38.p12 chr9: 34,474,793-34,477,226 DNAI1, RN7SKP24
    nsv4828243copy number variation1nstd200human GRCh37 chr9: 34,473,344-34,475,018 , GRCh38.p12 chr9: 34,473,346-34,475,020 DNAI1
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