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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5694432mobile element insertion2nstd211human GRCh38 chr9: 121,194,628-121,194,628 , GRCh37.p13 chr9: 123,956,906-123,956,906 RAB14
    nsv5545913insertion1nstd206human GRCh38 chr9: 121,181,027-121,181,077 , GRCh37.p13 chr9: 123,943,305-123,943,355 RAB14
    nsv5485367copy number variation1nstd206human GRCh38 chr9: 121,179,387-121,179,517 , GRCh37.p13 chr9: 123,941,665-123,941,795 RAB14
    nsv5394711mobile element insertion1nstd206human GRCh38 chr9: 121,194,628-121,194,679 , GRCh37.p13 chr9: 123,956,906-123,956,957 RAB14
    nsv5139463mobile element insertion1nstd203human GRCh38 chr9: 121,194,617-121,194,628 , GRCh37.p13 chr9: 123,956,895-123,956,906 RAB14
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983507copy number variation1nstd200human GRCh38 chr9: 121,194,744-121,195,686 , GRCh37.p13 chr9: 123,957,022-123,957,964 RAB14
    nsv4496385mobile element insertion1nstd166human GRCh37.p13 chr9: 123,962,278-123,962,278 , GRCh38.p12 chr9: 121,200,000-121,200,000 GSN, RAB14
    nsv4482805mobile element insertion1nstd166human GRCh37.p13 chr9: 123,956,895-123,956,895 , GRCh38.p12 chr9: 121,194,617-121,194,617 RAB14
    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
    nsv4343265sequence alteration1nstd166human GRCh37.p13 chr9: 123,579,171-124,453,597 , GRCh38.p12 chr9: 120,816,893-121,691,318 C5, GSN, 17 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
    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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