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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5597008copy number variation1nstd207human GRCh38 chr9: 122,391,309-122,391,361 , GRCh37.p13 chr9: 125,153,588-125,153,640 PTGS1
    nsv5483613copy number variation1nstd206human GRCh38 chr9: 122,376,093-122,376,156 , GRCh37.p13 chr9: 125,138,372-125,138,435 PTGS1
    nsv5206201mobile element deletion1nstd204human GRCh38.p13 chr9: 122,389,132-122,389,458 , GRCh37.p13 chr9: 125,151,411-125,151,737 PTGS1
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4771281mobile element deletion1nstd200human GRCh37 chr9: 125,151,420-125,151,729 , GRCh38.p12 chr9: 122,389,141-122,389,450 PTGS1
    nsv4728975copy number variation1nstd102humanLikely benign GRCh37 chr9: 125,154,228-125,339,689 , GRCh38.p12 chr9: 122,391,949-122,577,410 PTGS1, OR1J4, 6 more genes
    nsv4676065copy number variation1nstd102humanUncertain significance GRCh37 chr9: 125,105,375-125,616,987 , GRCh38.p12 chr9: 122,343,096-122,854,708 OR1L3, OR1N1, 19 more genes
    nsv4675789copy number variation1nstd102humanUncertain significance GRCh37 chr9: 124,604,592-126,306,080 , GRCh38.p12 chr9: 121,842,313-123,543,801 MIR7150, OR1N2, 43 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
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4179741copy number variation1nstd166human GRCh37.p13 chr9: 125,030,455-125,139,517 , GRCh38.p12 chr9: 122,268,176-122,377,238 PTGS1, MRRF
    nsv4179296copy number variation1nstd166human GRCh37.p13 chr9: 125,153,025-125,346,950 , GRCh38.p12 chr9: 122,390,746-122,584,671 PTGS1, OR1J4, 6 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
    nsv3921598copy number variation1nstd102humanPathogenic GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389 PGAP4, ECPAS, 2167 more genes
    nsv3920829copy number variation1nstd102humanPathogenic GRCh38 chr9: 121,112,395-138,075,224 , GRCh37 chr9: 123,874,673-140,969,676 , NCBI36 chr9: 122,914,494-140,089,497 LOC101928786, NRON, 495 more genes
    nsv3920713copy number variation1nstd102humanPathogenic NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389 ABHD17B, LOC100533707, 2167 more genes
    nsv3919257copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718 LOC107987031, LOC105376234, 2169 more genes
    nsv3918439copy number variation1nstd102humanPathogenic GRCh38 chr9: 121,073,102-138,179,445 , GRCh37 chr9: 123,835,380-141,073,897 , NCBI36 chr9: 122,875,201-140,193,718 MIR4478, ENTR1, 498 more genes
    nsv3917022copy number variation1nstd102humanPathogenic GRCh37 chr9: 214,367-141,008,915 , GRCh38 chr9: 193,412-138,114,463 , NCBI36 chr9: 204,367-140,128,736 RN7SKP87, SPATA6L, 2168 more genes
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