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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137702copy number variation1nstd102humanPathogenic GRCh37 chr9: 35,059,633-37,660,586 , GRCh38.p12 chr9: 35,059,636-37,660,589 ARHGEF39, LOC105376026, 84 more genes
    nsv6137700copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,088,563-39,092,820 , GRCh38.p12 chr9: 36,088,566-39,092,823 SNX18P3, VN1R48P, 69 more genes
    nsv5861912copy number variation1nstd209human GRCh38 chr9: 36,085,011-36,086,210 , GRCh37.p13 chr9: 36,085,008-36,086,207 RECK
    nsv5711819mobile element insertion1nstd211human GRCh38 chr9: 36,123,372-36,123,372 , GRCh37.p13 chr9: 36,123,369-36,123,369 RECK
    nsv5709757mobile element insertion1nstd211human GRCh38 chr9: 36,108,318-36,108,318 , GRCh37.p13 chr9: 36,108,315-36,108,315 RECK
    nsv5709739mobile element insertion1nstd211human GRCh38 chr9: 36,070,550-36,070,550 , GRCh37.p13 chr9: 36,070,547-36,070,547 RECK
    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
    nsv5486608copy number variation1nstd206human GRCh38 chr9: 36,035,069-36,035,183 , GRCh37.p13 chr9: 36,035,066-36,035,180 RECK
    nsv5413354mobile element insertion1nstd206human GRCh38 chr9: 36,070,550-36,070,601 , GRCh37.p13 chr9: 36,070,547-36,070,598 RECK
    nsv5407729mobile element insertion1nstd206human GRCh38 chr9: 36,108,318-36,108,369 , GRCh37.p13 chr9: 36,108,315-36,108,366 RECK
    nsv5399326mobile element insertion1nstd206human GRCh38 chr9: 36,123,372-36,123,423 , GRCh37.p13 chr9: 36,123,369-36,123,420 RECK
    nsv5381659copy number variation1nstd102humanUncertain significance GRCh37 chr9: 35,683,146-36,277,049 , GRCh38.p12 chr9: 35,683,149-36,277,052 CREB3, GBA2, 30 more genes
    nsv5127384mobile element insertion1nstd203human GRCh38 chr9: 36,123,359-36,123,372 , GRCh37.p13 chr9: 36,123,356-36,123,369 RECK
    nsv5122967mobile element insertion1nstd203human GRCh38 chr9: 36,123,358-36,123,372 , GRCh37.p13 chr9: 36,123,355-36,123,369 RECK
    nsv5121382mobile element insertion1nstd203human GRCh38 chr9: 36,108,316-36,108,330 , GRCh37.p13 chr9: 36,108,313-36,108,327 RECK
    nsv4964330copy number variation1nstd200human GRCh38 chr9: 36,035,069-36,035,183 , GRCh37.p13 chr9: 36,035,066-36,035,180 RECK
    nsv4828278copy number variation1nstd200human GRCh37 chr9: 36,035,066-36,035,180 , GRCh38.p12 chr9: 36,035,069-36,035,183 RECK
    nsv4766654inversion1nstd199human GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552 , ACO1, 876 more genes
    nsv4755256inversion1nstd199human GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552 , ACO1, 876 more genes
    nsv4729230copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 32,192,406-38,311,776 , GRCh38.p12 chr9: 32,192,408-38,311,779 ACO1, ANXA2P2, 210 more genes
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