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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5916921copy number variation1nstd209human GRCh38 chr7: 603,638-603,754 , GRCh37.p13 chr7: 643,275-643,391 PRKAR1B, PRKAR1B-AS1
    nsv5914093copy number variation1nstd209human GRCh38 chr7: 608,627-609,015 , GRCh37.p13 chr7: 648,264-648,652 PRKAR1B, PRKAR1B-AS1
    nsv5638262insertion1nstd207human GRCh38 chr7: 608,758-608,758 , GRCh37.p13 chr7: 648,395-648,395 PRKAR1B-AS1, PRKAR1B
    nsv5633559insertion2nstd207human GRCh38 chr7: 608,596-608,596 , GRCh37.p13 chr7: 648,233-648,233 PRKAR1B-AS1, PRKAR1B
    nsv5628993insertion1nstd207human GRCh38 chr7: 603,598-603,598 , GRCh37.p13 chr7: 643,235-643,235 PRKAR1B, PRKAR1B-AS1
    nsv5627858insertion1nstd207human GRCh38 chr7: 603,814-603,814 , GRCh37.p13 chr7: 643,451-643,451 PRKAR1B, PRKAR1B-AS1
    nsv5578089copy number variation1nstd207human GRCh38 chr7: 608,628-608,887 , GRCh37.p13 chr7: 648,265-648,524 PRKAR1B-AS1, PRKAR1B
    nsv5569604copy number variation1nstd207human GRCh38 chr7: 608,995-609,059 , GRCh37.p13 chr7: 648,632-648,696 PRKAR1B, PRKAR1B-AS1
    nsv5568463copy number variation1nstd207human GRCh38 chr7: 608,598-608,662 , GRCh37.p13 chr7: 648,235-648,299 PRKAR1B-AS1, PRKAR1B
    nsv4966149copy number variation1nstd200human GRCh38 chr7: 535,382-699,021 , GRCh37.p13 chr7: 575,019-738,658 LOC105375119, PRKAR1B-AS1, 2 more genes
    nsv4764656insertion1nstd199human GRCh37 chr7: 643,452-643,452 , GRCh38.p12 chr7: 603,815-603,815 PRKAR1B, PRKAR1B-AS1
    nsv4679604copy number variation1nstd189human GRCh37.p13 chr7: 518,519-745,398 , GRCh38.p12 chr7: 478,882-705,761 PDGFA, PRKAR1B, 4 more genes
    nsv4675871copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-1,750,797 , GRCh38.p12 chr7: 44,935-1,711,161 C7orf50, LOC105375123, 47 more genes
    nsv4675301copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-1,648,288 , GRCh38.p12 chr7: 43,360-1,608,652 LOC112267991, MICALL2, 42 more genes
    nsv4456827copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,376-19,520,619 , GRCh38.p12 chr7: 43,376-19,480,996 MIR6836, EEF1A1P26, 277 more genes
    nsv4456136copy number variation1nstd102humanPathogenic GRCh37 chr7: 36,616-4,298,168 , GRCh38.p12 chr7: 36,616-4,258,536 LOC442497, LFNG, 85 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4446738copy number variation1nstd175human GRCh37 chr7: 648,632-648,697 , GRCh38.p12 chr7: 608,995-609,060 PRKAR1B, PRKAR1B-AS1
    nsv4443042insertion1nstd175human GRCh37 chr7: 643,451-643,451 , GRCh38.p12 chr7: 603,814-603,814 PRKAR1B, PRKAR1B-AS1
    nsv4376782copy number variation1nstd173human GRCh37 chr7: 230,908-941,749 , GRCh38.p12 chr7: 230,908-902,112 PRKAR1B-AS1, LOC105375119, 15 more genes
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