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Items: 1 to 20 of 294

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068350inversion1nstd229human GRCh38 chr9: 83,044,445-83,044,475 , GRCh37.p13 chr9: 85,659,360-85,659,390 RASEF
    nsv7066601inversion1nstd229human GRCh38 chr9: 83,036,255-83,036,322 , GRCh37.p13 chr9: 85,651,170-85,651,237 RASEF
    nsv6874990copy number variation1nstd229human GRCh38 chr9: 83,018,489-83,018,516 , GRCh37.p13 chr9: 85,633,404-85,633,431 RASEF
    nsv6873343copy number variation1nstd229human GRCh38 chr9: 82,980,773-82,983,722 , GRCh37.p13 chr9: 85,595,688-85,598,637 RASEF
    nsv6871728copy number variation1nstd229human GRCh38 chr9: 82,951,950-83,142,523 , GRCh37.p13 chr9: 85,566,865-85,757,438 RASEF
    nsv6871089copy number variation1nstd229human GRCh38 chr9: 82,803,091-83,174,770 , GRCh37.p13 chr9: 85,418,006-85,789,685 RASEF
    nsv6863202copy number variation1nstd229human GRCh38 chr9: 82,586,753-83,344,977 , GRCh37.p13 chr9: 85,201,668-85,959,892 LOC105376110, RASEF, 6 more genes
    nsv6859786copy number variation1nstd229human GRCh38 chr9: 83,024,035-83,031,032 , GRCh37.p13 chr9: 85,638,950-85,645,947 RASEF
    nsv6858300copy number variation1nstd229human GRCh38 chr9: 83,044,676-83,045,082 , GRCh37.p13 chr9: 85,659,591-85,659,997 RASEF
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6574515inversion1nstd223human GRCh38 chr9: 83,029,417-83,030,209 , GRCh37.p13 chr9: 85,644,332-85,645,124 RASEF
    nsv6568042inversion1nstd223human GRCh38 chr9: 77,399,209-87,276,767 , GRCh37.p13 chr9: 80,014,125-89,891,682 , LOC105376119, 118 more genes
    nsv6453331copy number variation1nstd223human GRCh38 chr9: 83,032,730-83,034,590 , GRCh37.p13 chr9: 85,647,645-85,649,505 RASEF
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6257838mobile element insertion1nstd215human GRCh38 chr9: 83,049,552-83,049,552 , GRCh37.p13 chr9: 85,664,467-85,664,467 RASEF
    nsv6147455mobile element deletion1nstd206human GRCh38 chr9: 83,049,534-83,055,592 , GRCh37.p13 chr9: 85,664,449-85,670,507 RASEF
    nsv6136848copy number variation1nstd213human GRCh37 chr9: 85,400,000-85,820,001 , GRCh38.p12 chr9: 82,785,085-83,205,086 RASEF, RN7SKP242
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