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Items: 1 to 20 of 289

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5650937insertion1nstd207human GRCh38 chr14: 104,729,510-104,729,510 , GRCh37.p13 chr14: 105,195,847-105,195,847 ADSS1
    nsv5645195insertion1nstd207human GRCh38 chr14: 104,729,716-104,729,716 , GRCh37.p13 chr14: 105,196,053-105,196,053 ADSS1
    nsv5589014copy number variation1nstd207human GRCh38 chr14: 104,729,535-104,729,587 , GRCh37.p13 chr14: 105,195,872-105,195,924 ADSS1
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv4991589copy number variation1nstd200human GRCh38 chr14: 104,735,541-104,741,606 , GRCh37.p13 chr14: 105,201,878-105,207,943 LOC107984670, ADSS1
    nsv4991588copy number variation1nstd200human GRCh38 chr14: 104,726,168-104,732,588 , GRCh37.p13 chr14: 105,192,505-105,198,925 ADSS1
    nsv4855126copy number variation1nstd200human GRCh37 chr14: 105,192,505-105,198,925 , GRCh38.p12 chr14: 104,726,168-104,732,588 ADSS1
    nsv4749948copy number variation1nstd199human GRCh37 chr14: 105,195,837-105,195,889 , GRCh38.p12 chr14: 104,729,500-104,729,552 ADSS1
    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
    nsv4728983copy number variation1nstd102humanUncertain significance GRCh37 chr14: 104,830,935-105,203,925 , GRCh38.p12 chr14: 104,364,598-104,737,588 C14orf180, TMEM179, 6 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
    nsv4675901copy number variation1nstd102humanUncertain significance GRCh37 chr14: 104,752,809-105,201,309 , GRCh38.p12 chr14: 104,286,472-104,734,972 TMEM179, LINC02280, 7 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
    nsv4675279copy number variation1nstd102humanUncertain significance GRCh37 chr14: 104,461,553-105,232,775 , GRCh38.p12 chr14: 103,995,216-104,766,438 MIR203A, ASPG, 18 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
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