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Items: 1 to 20 of 318

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130409insertion1nstd186human GRCh37 chr12: 132,401,820-132,401,872 , GRCh38.p12 chr12: 131,917,275-131,917,327 ULK1
    nsv6129169insertion1nstd186human GRCh37 chr12: 132,401,835-132,401,857 , GRCh38.p12 chr12: 131,917,290-131,917,312 ULK1
    nsv5979503inversion1nstd209human GRCh38 chr12: 131,622,778-131,899,766 , GRCh37.p13 chr12: 132,107,323-132,384,311 MMP17, SFSWAP, 10 more genes
    nsv5968705inversion1nstd209human GRCh38 chr12: 131,807,431-132,059,968 , GRCh37.p13 chr12: 132,291,976-132,544,513 MMP17, ULK1, 6 more genes
    nsv5933115copy number variation1nstd209human GRCh38 chr12: 131,906,336-131,906,468 , GRCh37.p13 chr12: 132,390,881-132,391,013 ULK1
    nsv5932568copy number variation1nstd209human GRCh38 chr12: 131,917,122-131,917,311 , GRCh37.p13 chr12: 132,401,667-132,401,856 ULK1
    nsv5864584copy number variation1nstd209human GRCh38 chr12: 131,912,499-131,914,730 , GRCh37.p13 chr12: 132,397,044-132,399,275 ULK1
    nsv5862010copy number variation1nstd209human GRCh38 chr12: 131,908,517-131,911,498 , GRCh37.p13 chr12: 132,393,062-132,396,043 ULK1
    nsv5663763insertion1nstd207human GRCh38 chr12: 131,917,084-131,917,084 , GRCh37.p13 chr12: 132,401,629-132,401,629 ULK1
    nsv5662691insertion1nstd207human GRCh38 chr12: 131,917,268-131,917,268 , GRCh37.p13 chr12: 132,401,813-132,401,813 ULK1
    nsv5658167insertion1nstd207human GRCh38 chr12: 131,917,187-131,917,187 , GRCh37.p13 chr12: 132,401,732-132,401,732 ULK1
    nsv5656764insertion1nstd207human GRCh38 chr12: 131,917,219-131,917,219 , GRCh37.p13 chr12: 132,401,764-132,401,764 ULK1
    nsv5653399insertion1nstd207human GRCh38 chr12: 131,917,207-131,917,207 , GRCh37.p13 chr12: 132,401,752-132,401,752 ULK1
    nsv5651523insertion1nstd207human GRCh38 chr12: 131,918,730-131,918,730 , GRCh37.p13 chr12: 132,403,275-132,403,275 ULK1
    nsv5651185insertion1nstd207human GRCh38 chr12: 131,917,283-131,917,283 , GRCh37.p13 chr12: 132,401,828-132,401,828 ULK1
    nsv5646491insertion1nstd207human GRCh38 chr12: 131,917,144-131,917,144 , GRCh37.p13 chr12: 132,401,689-132,401,689 ULK1
    nsv5556389sequence alteration1nstd206human GRCh38 chr12: 131,556,124-132,287,086 , GRCh37.p13 chr12: 132,040,669-132,706,992 , ULK1, 25 more genes
    nsv5547647insertion1nstd206human GRCh38 chr12: 131,917,275-131,917,327 , GRCh37.p13 chr12: 132,401,820-132,401,872 ULK1
    nsv5536312insertion1nstd206human GRCh38 chr12: 131,917,290-131,917,312 , GRCh37.p13 chr12: 132,401,835-132,401,857 ULK1
    nsv5509451copy number variation1nstd206human GRCh38 chr12: 131,906,507-131,907,264 , GRCh37.p13 chr12: 132,391,052-132,391,809 ULK1
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