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Items: 1 to 20 of 268

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5947014copy number variation1nstd209human GRCh38 chr13: 113,876,678-113,876,728 , GRCh37.p13 chr13: 114,579,651-114,579,701 LINC00454
    nsv5942029copy number variation1nstd209human GRCh38 chr13: 113,883,430-113,883,630 , GRCh37.p13 chr13: 114,586,403-114,586,603 LINC00454
    nsv5653620insertion1nstd207human GRCh38 chr13: 113,876,729-113,876,729 , GRCh37.p13 chr13: 114,579,702-114,579,702 LINC00454
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5503151copy number variation1nstd206human GRCh38 chr13: 113,871,335-114,124,231 , GRCh37.p13 chr13: 114,574,308-114,889,706 , RASA3, 6 more genes
    nsv5393099copy number variation1nstd186human GRCh37 chr13: 114,579,089-114,579,628 , GRCh38.p12 chr13: 113,876,116-113,876,655 LINC00454
    nsv5392815copy number variation1nstd186human GRCh37 chr13: 114,579,127-114,579,645 , GRCh38.p12 chr13: 113,876,154-113,876,672 LINC00454
    nsv5349003translocation1nstd200human GRCh38 chr13: 113,876,729-113,876,729 , GRCh38 chr13: 113,876,439-113,876,439 , GRCh37.p13 chr13: 114,579,412-114,579,412 , GRCh37.p13 chr13: 114,579,702-114,579,702 LINC00454
    nsv5337407translocation1nstd200human GRCh37 chr13: 114,579,702-114,579,702 , GRCh37 chr13: 114,579,412-114,579,412 , GRCh38.p12 chr13: 113,876,439-113,876,439 , GRCh38.p12 chr13: 113,876,729-113,876,729 LINC00454
    nsv5319592copy number variation1nstd204human GRCh38.p13 chr13: 113,876,439-113,876,729 , GRCh37.p13 chr13: 114,579,412-114,579,702 LINC00454
    nsv5305564copy number variation1nstd204human GRCh38.p13 chr13: 113,876,163-113,876,650 , GRCh37.p13 chr13: 114,579,136-114,579,623 LINC00454
    nsv5300592copy number variation1nstd204human GRCh38.p13 chr13: 113,883,576-113,883,694 , GRCh37.p13 chr13: 114,586,549-114,586,667 LINC00454
    nsv5275188copy number variation1nstd204human GRCh38.p13 chr13: 113,876,372-113,889,246 , GRCh37.p13 chr13: 114,579,345-114,592,219 LINC00454
    nsv5272817copy number variation1nstd204human GRCh38.p13 chr13: 113,876,401-113,876,700 , GRCh37.p13 chr13: 114,579,374-114,579,673 LINC00454
    nsv5269303copy number variation1nstd204human GRCh38.p13 chr13: 113,775,801-114,100,000 , GRCh37.p13 chr13: 114,478,774-114,865,475 , GAS6, 8 more genes
    nsv5007136copy number variation1nstd200human GRCh38 chr13: 113,881,717-113,881,953 , GRCh37.p13 chr13: 114,584,690-114,584,926 LINC00454
    nsv4994038copy number variation1nstd200human GRCh38 chr13: 113,876,066-113,876,696 , GRCh37.p13 chr13: 114,579,039-114,579,669 LINC00454
    nsv4994033copy number variation1nstd200human GRCh38 chr13: 113,792,082-113,937,362 , GRCh37.p13 chr13: 114,495,055-114,639,948 , GAS6, 6 more genes
    nsv4839281copy number variation1nstd200human GRCh37 chr13: 114,579,078-114,579,715 , GRCh38.p12 chr13: 113,876,105-113,876,742 LINC00454
    nsv4769247copy number variation1nstd201human GRCh37 chr13: 109,490,236-115,107,733 , GRCh38.p12 chr13: 108,837,888-114,342,258 , PARP1P1, 117 more genes
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