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Items: 1 to 20 of 104

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098049copy number variation1nstd102humanUncertain significance GRCh37 chr9: 116,037,910-116,993,432 , GRCh38.p12 chr9: 113,275,630-114,231,152 POLE3, LOC100132609, 20 more genes
    nsv7097922copy number variation1nstd102humanUncertain significance GRCh37 chr9: 116,037,910-116,038,070 , GRCh38.p12 chr9: 113,275,630-113,275,790 CDC26, PRPF4
    nsv6863631copy number variation1nstd229human GRCh38 chr9: 113,185,401-113,334,700 , GRCh37.p13 chr9: 115,947,681-116,096,980 RNF183, FKBP15, 5 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
    nsv6633305copy number variation1nstd224human GRCh37 chr9: 115,861,201-116,125,789 , GRCh38.p12 chr9: 113,098,921-113,363,509 SLC31A2, BSPRY, 9 more genes
    nsv6567241inversion1nstd223human GRCh38 chr9: 113,264,667-113,265,543 , GRCh37.p13 chr9: 116,026,947-116,027,823 CDC26, SLC31A1
    nsv6565934inversion1nstd223human GRCh38 chr9: 113,264,593-113,265,631 , GRCh37.p13 chr9: 116,026,873-116,027,911 SLC31A1, CDC26
    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
    nsv6313987copy number variation1nstd102humanUncertain significance GRCh37 chr9: 115,883,313-116,179,965 , GRCh38.p12 chr9: 113,121,033-113,417,685 HDHD3, BSPRY, 11 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
    nsv6136358copy number variation1nstd213human GRCh37 chr9: 115,820,000-116,410,001 , GRCh38.p12 chr9: 113,057,720-113,647,721 RGS3, PRPF4, 16 more genes
    nsv6004054copy number variation1nstd212human GRCh38 chr9: 113,268,819-113,268,886 , GRCh37.p13 chr9: 116,031,099-116,031,166 CDC26
    nsv5131488mobile element insertion1nstd203human GRCh38 chr9: 113,267,549-113,267,566 , GRCh37.p13 chr9: 116,029,829-116,029,846 CDC26
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4489408mobile element insertion1nstd166human GRCh37.p13 chr9: 116,034,833-116,034,833 , GRCh38.p12 chr9: 113,272,553-113,272,553 CDC26
    nsv4457284copy number variation1nstd102humanUncertain significance GRCh37 chr9: 116,034,704-116,199,658 , GRCh38.p12 chr9: 113,272,424-113,437,378 RNF183, C9orf43, 7 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
    nsv4456379copy number variation1nstd102humanUncertain significance GRCh37 chr9: 113,982,711-117,443,628 , GRCh38.p12 chr9: 111,220,431-114,681,348 MIR4668, LOC100418705, 74 more genes
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