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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148263copy number variation1nstd102humanPathogenic GRCh38 chr9: 102,995,214-108,903,040 , GRCh37.p13 chr9: 105,757,496-111,665,320 ACTL7B, OR13C3, 88 more genes
    nsv7076361inversion1nstd229human GRCh38 chr9: 104,601,460-104,617,602 , GRCh37.p13 chr9: 107,363,741-107,379,883 OR13C9, OR13C2
    nsv6876203copy number variation1nstd229human GRCh38 chr9: 104,505,384-104,652,917 , GRCh37.p13 chr9: 107,267,665-107,415,198 OR13C4, OR13C8, 7 more genes
    nsv6875208copy number variation1nstd229human GRCh38 chr9: 104,605,501-104,618,700 , GRCh37.p13 chr9: 107,367,782-107,380,981 OR13C2, OR13C9
    nsv6865784copy number variation1nstd229human GRCh38 chr9: 104,605,390-104,618,014 , GRCh37.p13 chr9: 107,367,671-107,380,295 OR13C9, OR13C2
    nsv6865343copy number variation1nstd229human GRCh38 chr9: 104,605,401-104,617,900 , GRCh37.p13 chr9: 107,367,682-107,380,181 OR13C9, OR13C2
    nsv6637573copy number variation1nstd102humanUncertain significance GRCh37 chr9: 106,173,402-107,431,515 , GRCh38.p12 chr9: 103,411,120-104,669,234 LOC105376194, TOPORSLP, 18 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6448405copy number variation1nstd223human GRCh38 chr9: 104,505,382-104,652,916 , GRCh37.p13 chr9: 107,267,663-107,415,197 OR13I1P, OR13C5, 7 more genes
    nsv6443875copy number variation1nstd223human GRCh38 chr9: 104,605,352-104,618,018 , GRCh37.p13 chr9: 107,367,633-107,380,299 OR13C2, OR13C9
    nsv6441550copy number variation1nstd223human GRCh38 chr9: 104,605,501-104,618,100 , GRCh37.p13 chr9: 107,367,782-107,380,381 OR13C9, OR13C2
    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
    nsv6302435copy number variation1nstd186human GRCh37 chr9: 107,368,281-107,380,833 , GRCh38.p12 chr9: 104,606,000-104,618,552 OR13C9, OR13C2
    nsv6290765copy number variation1nstd102humanUncertain significance GRCh37 chr9: 102,858,276-110,624,997 , GRCh38.p12 chr9: 100,095,994-107,862,716 RNF20, SMC2, 120 more genes
    nsv6137323copy number variation1nstd213human GRCh37 chr9: 107,030,000-107,660,001 , GRCh38.p12 chr9: 104,267,719-104,897,720 OR13C5, OR13C8, 18 more genes
    nsv5856503copy number variation1nstd209human GRCh38 chr9: 104,608,966-104,617,977 , GRCh37.p13 chr9: 107,371,247-107,380,258 OR13C9
    nsv5850445copy number variation1nstd209human GRCh38 chr9: 104,608,466-104,616,250 , GRCh37.p13 chr9: 107,370,747-107,378,531 OR13C9
    nsv5490651copy number variation1nstd206human GRCh38 chr9: 104,605,038-104,618,552 , GRCh37.p13 chr9: 107,367,319-107,380,833 OR13C9, OR13C2
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