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Items: 1 to 20 of 265

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971389insertion1nstd209human GRCh38 chr17: 76,416,180-76,416,180 , GRCh37.p13 chr17: 74,412,262-74,412,262 UBE2O
    nsv5707099mobile element insertion1nstd211human GRCh38 chr17: 76,425,241-76,425,241 , GRCh37.p13 chr17: 74,421,323-74,421,323 UBE2O
    nsv5551747insertion1nstd206human GRCh38 chr17: 76,416,269-76,416,269 , GRCh37.p13 chr17: 74,412,351-74,412,351 UBE2O
    nsv5548687insertion1nstd206human GRCh38 chr17: 76,448,241-76,448,241 , GRCh37.p13 chr17: 74,444,323-74,444,323 UBE2O
    nsv5530378copy number variation1nstd206human GRCh38 chr17: 76,433,728-76,443,992 , GRCh37.p13 chr17: 74,429,810-74,440,074 UBE2O
    nsv5529457copy number variation1nstd206human GRCh38 chr17: 76,429,396-76,431,440 , GRCh37.p13 chr17: 74,425,478-74,427,522 RPL7P49, UBE2O
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
    nsv5153179mobile element insertion1nstd203human GRCh38 chr17: 76,441,592-76,441,604 , GRCh37.p13 chr17: 74,437,674-74,437,686 UBE2O
    nsv4680180copy number variation1nstd189human GRCh37.p13 chr17: 74,053,616-74,648,486 , GRCh38.p12 chr17: 76,057,535-76,652,404 , AANAT, 30 more genes
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4628562copy number variation1nstd183human GRCh37 chr17: 74,406,128-74,414,286 , GRCh38.p12 chr17: 76,410,046-76,418,204 UBE2O
    nsv4548520insertion1nstd166human GRCh37.p13 chr17: 74,389,866-74,389,866 , GRCh38.p12 chr17: 76,393,785-76,393,785 UBE2O
    nsv4502831mobile element insertion1nstd166human GRCh37.p13 chr17: 74,437,891-74,437,891 , GRCh38.p12 chr17: 76,441,809-76,441,809 UBE2O
    nsv4457881copy number variation1nstd102humanUncertain significance GRCh37 chr17: 74,401,337-74,574,103 , GRCh38.p12 chr17: 76,405,256-76,578,021 SNHG16, PRCD, 9 more genes
    nsv4457850copy number variation1nstd102humanUncertain significance GRCh37 chr17: 74,286,105-74,413,899 , GRCh38.p12 chr17: 76,290,024-76,417,817 RNU6-24P, PRPSAP1, 4 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4322217insertion1nstd166human GRCh37.p13 chr17: 74,412,342-74,412,342 , GRCh38.p12 chr17: 76,416,260-76,416,260 UBE2O
    nsv4261082copy number variation1nstd166human GRCh37.p13 chr17: 74,425,631-74,425,831 , GRCh38.p12 chr17: 76,429,549-76,429,749 UBE2O, RPL7P49
    nsv4258989copy number variation1nstd166human GRCh37.p13 chr17: 74,430,061-74,432,902 , GRCh38.p12 chr17: 76,433,979-76,436,820 UBE2O
    nsv4258269copy number variation1nstd166human GRCh37.p13 chr17: 74,415,000-74,421,000 , GRCh38.p12 chr17: 76,418,918-76,424,918 UBE2O
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