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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6874906copy number variation1nstd229human GRCh38 chr9: 111,555,501-111,653,300 , GRCh37.p13 chr9: 114,317,781-114,415,580 ZNF483, DNAJC25-GNG10, 4 more genes
    nsv6873360copy number variation1nstd229human GRCh38 chr9: 111,494,875-111,906,695 , GRCh37.p13 chr9: 114,257,155-114,668,975 ZNF483, GNG10, 8 more genes
    nsv6867147copy number variation1nstd229human GRCh38 chr9: 111,569,993-111,605,081 , GRCh37.p13 chr9: 114,332,273-114,367,361 ZNF483, PTGR1, 1 more genes
    nsv6861299copy number variation1nstd229human GRCh38 chr9: 111,610,355-111,621,365 , GRCh37.p13 chr9: 114,372,635-114,383,645 LRRC37A5P
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6435848copy number variation1nstd223human GRCh38 chr9: 111,604,541-111,607,287 , GRCh37.p13 chr9: 114,366,821-114,369,567 LRRC37A5P
    nsv6315460copy number variation1nstd102humanUncertain significance GRCh37 chr9: 113,673,200-115,935,268 , GRCh38.p12 chr9: 110,910,920-113,172,988 MIR4668, LINC02977, 40 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
    nsv6314062copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 109,265,628-117,650,999 , GRCh38.p12 chr9: 106,503,347-114,888,719 ALAD, AMBP, 151 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
    nsv6137435copy number variation1nstd213human GRCh37 chr9: 114,290,000-114,910,001 , GRCh38.p12 chr9: 111,527,720-112,147,721 PTGR1, DNAJC25-GNG10, 13 more genes
    nsv6136726copy number variation1nstd213human GRCh37 chr9: 114,140,000-114,620,001 , GRCh38.p12 chr9: 111,377,720-111,857,721 ECPAS, LOC107987116, 9 more genes
    nsv6136639copy number variation1nstd213human GRCh37 chr9: 114,260,000-114,500,001 , GRCh38.p12 chr9: 111,497,720-111,737,721 GNG10, PTGR1, 6 more genes
    nsv5924410copy number variation1nstd209human GRCh38 chr9: 111,494,845-111,906,694 , GRCh37.p13 chr9: 114,257,125-114,668,974 UGCG, PTGR1, 8 more genes
    nsv5640749insertion1nstd207human GRCh38 chr9: 111,600,860-111,600,860 , GRCh37.p13 chr9: 114,363,140-114,363,140 LRRC37A5P
    nsv5259668copy number variation1nstd204human GRCh38.p13 chr9: 111,607,703-111,611,856 , GRCh37.p13 chr9: 114,369,983-114,374,136 LRRC37A5P
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4525533copy number variation1nstd166human GRCh37.p13 chr9: 114,360,902-114,390,470 , GRCh38.p12 chr9: 111,598,622-111,628,190 PTGR1, LRRC37A5P, 1 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
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