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Items: 1 to 20 of 284

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5500370copy number variation1nstd206human GRCh38 chr14: 104,800,549-104,800,812 , GRCh37.p13 chr14: 105,266,886-105,267,149 ZBTB42
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5357643translocation1nstd200human GRCh38 chr14: 104,803,026-104,803,026 , GRCh38 chr14: 104,803,087-104,803,087 , GRCh37.p13 chr14: 105,269,424-105,269,424 , GRCh37.p13 chr14: 105,269,363-105,269,363 ZBTB42
    nsv5340382translocation1nstd200human GRCh37 chr14: 105,269,363-105,269,363 , GRCh37 chr14: 105,269,424-105,269,424 , GRCh38.p12 chr14: 104,803,026-104,803,026 , GRCh38.p12 chr14: 104,803,087-104,803,087 ZBTB42
    nsv5005040copy number variation1nstd200human GRCh38 chr14: 104,782,003-104,804,453 , GRCh37.p13 chr14: 105,248,340-105,270,790 ZBTB42, AKT1
    nsv4863626copy number variation1nstd200human GRCh37 chr14: 105,248,340-105,270,790 , GRCh38.p12 chr14: 104,782,003-104,804,453 ZBTB42, AKT1
    nsv4729298copy number variation1nstd102humanUncertain significance GRCh37 chr14: 105,112,467-105,285,280 , GRCh38.p12 chr14: 104,646,130-104,818,943 LOC102723342, ZBTB42, 8 more genes
    nsv4729218copy number variation1nstd102humanPathogenic GRCh37 chr14: 102,615,953-107,285,437 , GRCh38.p12 chr14: 102,149,616-106,877,229 IGHV4-61, IGHD3-9, 308 more genes
    nsv4728966copy number variation1nstd102humanUncertain significance GRCh37 chr14: 105,204,147-105,543,486 , GRCh38.p12 chr14: 104,737,810-105,077,149 CLBA1, ZBTB42, 15 more genes
    nsv4684265copy number variation1nstd102humanPathogenic GRCh37 chr14: 96,829,290-107,287,663 , GRCh38.p12 chr14: 96,362,953-106,879,456 NDUFB3P4, LINC02320, 502 more genes
    nsv4681219copy number variation1nstd102humanPathogenic GRCh37 chr14: 105,143,996-105,424,009 , GRCh38.p12 chr14: 104,677,659-104,957,672 INF2, SIVA1, 14 more genes
    nsv4675524copy number variation1nstd102humanPathogenic GRCh37 chr14: 104,764,078-107,285,437 , GRCh38.p12 chr14: 104,297,741-106,877,229 IGHV3-76, IGHV5-10-1, 241 more genes
    nsv4624902copy number variation1nstd183human GRCh37 chr14: 103,676,460-105,831,463 , GRCh38.p12 chr14: 103,210,123-105,365,126 , ZFYVE21, 69 more genes
    nsv4624595copy number variation1nstd183human GRCh37 chr14: 104,929,882-106,342,979 , GRCh38.p12 chr14: 104,466,471-105,877,120 , IGHJ2, 73 more genes
    nsv4456944copy number variation1nstd102humanPathogenic GRCh37 chr14: 101,627,916-107,147,698 , GRCh38.p12 chr14: 101,161,579-106,691,681 IGHV1-58, IGHVII-60-1, 308 more genes
    nsv4456320copy number variation1nstd102humanPathogenic GRCh37 chr14: 102,931,119-107,285,437 , GRCh38.p12 chr14: 102,464,782-106,877,229 LOC105378184, LINC02298, 302 more genes
    nsv4456178copy number variation1nstd102humanPathogenic GRCh37 chr14: 91,969,028-107,285,437 , GRCh38.p12 chr14: 91,502,684-106,877,229 LOC105370639, SERPINA9, 600 more genes
    nsv4455831copy number variation1nstd102humanUncertain significance GRCh37 chr14: 105,067,651-107,285,437 , GRCh38.p12 chr14|NT_187600.1: 1-1,214,078 , GRCh38.p12 chr14: 104,622,881-106,877,229 VESTAR, IGHVIII-25-1, 238 more genes
    nsv4455156copy number variation1nstd102humanPathogenic GRCh37 chr14: 99,794,230-107,285,437 , GRCh38.p12 chr14: 99,327,893-106,877,229 IGHG4, IGHV3-57, 464 more genes
    nsv4436056complex substitution1nstd102humanUncertain significance GRCh38.p12 chr14: 104,177,384-105,466,438 , GRCh37 chr14: 104,643,721-105,932,775 AKT1, BRF1, 35 more genes
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