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Items: 1 to 20 of 242

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5908456copy number variation1nstd209human GRCh38 chr9: 34,549,821-34,549,875 , GRCh37.p13 chr9: 34,549,819-34,549,873 CNTFR
    nsv5674074copy number variation1nstd102humanPathogenic GRCh37 chr9: 34,459,004-36,276,941 , GRCh38.p12 chr9: 34,459,006-36,276,944 SPAG8, DNAI1, 84 more genes
    nsv5585662copy number variation1nstd207human GRCh38 chr9: 34,549,821-34,549,875 , GRCh37.p13 chr9: 34,549,819-34,549,873 CNTFR
    nsv5493723copy number variation1nstd206human GRCh38 chr9: 34,549,823-34,549,876 , GRCh37.p13 chr9: 34,549,821-34,549,874 CNTFR
    nsv5493133copy number variation1nstd206human GRCh38 chr9: 34,574,250-34,574,324 , GRCh37.p13 chr9: 34,574,248-34,574,322 CNTFR, CNTFR-AS1
    nsv5381707copy number variation2nstd102humanUncertain significance GRCh37 chr9: 34,458,994-35,072,710 , GRCh38.p12 chr9: 34,458,996-35,072,713 YWHAZP6, IL11RA, 30 more genes
    nsv4964281copy number variation1nstd200human GRCh38 chr9: 34,574,552-34,593,528 , GRCh37.p13 chr9: 34,574,550-34,593,526 CNTFR, CNTFR-AS1
    nsv4954662copy number variation1nstd200human GRCh38 chr9: 34,586,119-34,588,042 , GRCh37.p13 chr9: 34,586,117-34,588,040 CNTFR
    nsv4954661copy number variation1nstd200human GRCh38 chr9: 34,568,023-34,569,246 , GRCh37.p13 chr9: 34,568,021-34,569,244 CNTFR, CNTFR-AS1, 1 more genes
    nsv4954657copy number variation1nstd200human GRCh38 chr9: 34,103,197-34,805,619 , GRCh37.p13 chr9: 34,103,195-34,805,616 , CCL27, 32 more genes
    nsv4828247copy number variation1nstd200human GRCh37 chr9: 34,574,550-34,593,526 , GRCh38.p12 chr9: 34,574,552-34,593,528 CNTFR, CNTFR-AS1
    nsv4766654inversion1nstd199human GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552 , ACO1, 876 more genes
    nsv4755256inversion1nstd199human GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552 , ACO1, 876 more genes
    nsv4732173copy number variation1nstd199human GRCh37 chr9: 34,549,821-34,549,876 , GRCh38.p12 chr9: 34,549,823-34,549,878 CNTFR
    nsv4729230copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 32,192,406-38,311,776 , GRCh38.p12 chr9: 32,192,408-38,311,779 ACO1, ANXA2P2, 210 more genes
    nsv4675565copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-70,984,588 , GRCh38.p12 chr9: 203,861-68,369,672 LOC100132004, LOC105375993, 853 more genes
    nsv4652067copy number variation1nstd186human GRCh37 chr9: 34,549,821-34,549,874 , GRCh38.p12 chr9: 34,549,823-34,549,876 CNTFR
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4457200copy number variation2nstd102humanPathogenic GRCh37 chr9: 203,861-67,986,965 , GRCh38.p12 chr9: 203,861-67,919,519 ACO1, RNU6-1073P, 846 more genes
    nsv4456028copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-38,472,979 , GRCh38.p12 chr9: 203,861-38,472,982 SNORA30B, LOC100419692, 559 more genes
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