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Items: 1 to 20 of 117

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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
    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
    nsv6870463copy number variation1nstd229human GRCh38 chr9: 104,387,838-104,554,257 , GRCh37.p13 chr9: 107,150,119-107,316,538 OR13F1, OR13C3, 2 more genes
    nsv6870421copy number variation1nstd229human GRCh38 chr9: 104,413,572-104,511,407 , GRCh37.p13 chr9: 107,175,853-107,273,688 LOC105376195, OR13F1
    nsv6858554copy number variation1nstd229human GRCh38 chr9: 104,486,501-104,502,400 , GRCh37.p13 chr9: 107,248,782-107,264,681 OR13F1
    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
    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
    nsv6307709mobile element insertion1nstd186human GRCh37 chr9: 107,267,588-107,267,639 , GRCh38.p12 chr9: 104,505,307-104,505,358 OR13F1
    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
    nsv5721391mobile element insertion2nstd211human GRCh38 chr9: 104,505,307-104,505,307 , GRCh37.p13 chr9: 107,267,588-107,267,588 OR13F1
    nsv5562107mobile element insertion1nstd206human GRCh38 chr9: 104,505,307-104,505,358 , GRCh37.p13 chr9: 107,267,588-107,267,639 OR13F1
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 RPS26P37, MIR27B, 238 more genes
    nsv4679196copy number variation1nstd189human GRCh37.p13 chr9: 107,061,882-107,737,966 , GRCh38.p12 chr9: 104,299,601-104,975,685 ABCA1, NIPSNAP3A, 18 more genes
    nsv4571558mobile element insertion1nstd166human GRCh37.p13 chr9: 107,267,573-107,267,573 , GRCh38.p12 chr9: 104,505,292-104,505,292 OR13F1
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