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Items: 1 to 20 of 139

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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
    nsv7077264inversion1nstd229human GRCh38 chr9: 107,230,971-107,507,293 , GRCh37.p13 chr9: 109,993,252-110,269,574 RAD23B, LOC107987110, 6 more genes
    nsv7074978inversion1nstd229human GRCh38 chr9: 106,755,903-108,407,110 , GRCh37.p13 chr9: 109,518,184-111,169,390 LOC105376209, LINC01509, 31 more genes
    nsv7072245inversion1nstd229human GRCh38 chr9: 107,492,197-107,576,903 , GRCh37.p13 chr9: 110,254,478-110,339,184 PPIAP88, LOC105376205, 1 more genes
    nsv6874739copy number variation1nstd229human GRCh38 chr9: 107,441,701-107,650,374 , GRCh37.p13 chr9: 110,203,982-110,412,655 RNU6-492P, KLF4, 5 more genes
    nsv6873365copy number variation1nstd229human GRCh38 chr9: 107,489,917-107,550,586 , GRCh37.p13 chr9: 110,252,198-110,312,867 KLF4, LOC105376206, 1 more genes
    nsv6871477copy number variation1nstd229human GRCh38 chr9: 107,346,001-107,556,200 , GRCh37.p13 chr9: 110,108,282-110,318,481 KLF4, LOC107987111, 5 more genes
    nsv6861684copy number variation1nstd229human GRCh38 chr9: 107,507,301-107,576,900 , GRCh37.p13 chr9: 110,269,582-110,339,181 PPIAP88, LOC105376206, 1 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
    nsv6632870copy number variation1nstd224human GRCh37 chr9: 110,241,529-110,303,463 , GRCh38.p12 chr9: 107,479,248-107,541,182 KLF4, PPIAP88, 1 more genes
    nsv6446869copy number variation1nstd223human GRCh38 chr9: 107,505,667-107,505,996 , GRCh37.p13 chr9: 110,267,948-110,268,277 LOC105376206
    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
    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
    nsv6137327copy number variation1nstd213human GRCh37 chr9: 109,340,000-112,470,001 , GRCh38.p12 chr9: 106,577,719-109,707,721 ACTL7A, TMEM245, 55 more genes
    nsv6136633copy number variation1nstd213human GRCh37 chr9: 110,220,000-110,410,001 , GRCh38.p12 chr9: 107,457,719-107,647,720 KLF4, HMGN2P32, 5 more genes
    nsv6136350copy number variation1nstd213human GRCh37 chr9: 109,820,000-110,360,001 , GRCh38.p12 chr9: 107,057,719-107,597,720 RAD23B, LOC340512, 11 more genes
    nsv5383888mobile element deletion1nstd186human GRCh37 chr9: 110,274,873-110,275,156 , GRCh38.p12 chr9: 107,512,592-107,512,875 LOC105376206
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