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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5974801inversion1nstd209human GRCh38 chr10: 116,446,135-119,236,441 , GRCh37.p13 chr10: 118,205,647-120,995,953 EMX2, PRLHR, 48 more genes
    nsv5672603copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 119,302,758-124,813,305 , GRCh38.p12 chr10: 117,543,247-123,053,789 ACADSB, DMBT1, 84 more genes
    nsv5511841copy number variation1nstd206human GRCh38 chr10: 119,066,368-119,340,368 , GRCh37.p13 chr10: 120,825,880-121,099,880 GRK5, EIF3A, 6 more genes
    nsv5499221copy number variation1nstd206human GRCh38 chr10: 119,165,528-119,165,758 , GRCh37.p13 chr10: 120,925,040-120,925,270 PRDX3, SFXN4
    nsv5311691copy number variation1nstd204human GRCh38.p13 chr10: 118,927,032-119,220,648 , GRCh37.p13 chr10: 120,686,544-120,980,160 GRK5-IT1, GRK5, 8 more genes
    nsv5257292copy number variation1nstd204human GRCh38.p13 chr10: 119,164,751-119,172,048 , GRCh37.p13 chr10: 120,924,263-120,931,560 SFXN4, PRDX3
    nsv5251707copy number variation1nstd204human GRCh38.p13 chr10: 118,927,101-119,220,000 , GRCh37.p13 chr10: 120,686,613-120,979,512 RN7SL749P, LDHAP5, 8 more genes
    nsv5213909mobile element deletion1nstd204human GRCh38.p13 chr10: 119,168,665-119,169,011 , GRCh37.p13 chr10: 120,928,177-120,928,523 PRDX3
    nsv4983933copy number variation1nstd200human GRCh38 chr10: 119,177,992-119,179,805 , GRCh37.p13 chr10: 120,937,504-120,939,317 PRDX3
    nsv4983932copy number variation1nstd200human GRCh38 chr10: 119,138,969-119,216,526 , GRCh37.p13 chr10: 120,898,481-120,976,038 RN7SL749P, GRK5-IT1, 3 more genes
    nsv4974095copy number variation1nstd200human GRCh38 chr10: 119,127,771-119,217,472 , GRCh37.p13 chr10: 120,887,283-120,976,984 RN7SL749P, GRK5-IT1, 4 more genes
    nsv4974089copy number variation1nstd200human GRCh38 chr10: 118,693,254-119,214,513 , GRCh37.p13 chr10: 120,452,766-120,974,025 EIF3A, RN7SL749P, 11 more genes
    nsv4899601mobile element deletion1nstd200human GRCh38 chr10: 119,168,694-119,168,983 , GRCh37.p13 chr10: 120,928,206-120,928,495 PRDX3
    nsv4774853mobile element deletion1nstd200human GRCh37 chr10: 120,928,206-120,928,495 , GRCh38.p12 chr10: 119,168,694-119,168,983 PRDX3
    nsv4729721copy number variation1nstd102humanLikely benign GRCh37 chr10: 120,937,348-121,168,413 , GRCh38.p12 chr10: 119,177,836-119,408,901 MIR4681, GRK5-IT1, 4 more genes
    nsv4675991copy number variation1nstd102humanPathogenic GRCh37 chr10: 119,996,339-135,427,143 , GRCh38.p12 chr10: 118,236,827-133,613,639 STK32C, LOC105378542, 237 more genes
    nsv4576120mobile element insertion1nstd166human GRCh37.p13 chr10: 120,927,248-120,927,248 , GRCh38.p12 chr10: 119,167,736-119,167,736 PRDX3
    nsv4456626copy number variation1nstd102humanPathogenic GRCh37 chr10: 114,544,537-135,427,143 , GRCh38.p12 chr10: 112,784,778-133,613,639 LOC105378521, ZRANB1, 317 more genes
    nsv4456176copy number variation1nstd102humanUncertain significance GRCh37 chr10: 120,933,323-121,007,499 , GRCh38.p12 chr10: 119,173,811-119,247,987 GRK5-IT1, RN7SL749P, 2 more genes
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