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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6126000copy number variation1nstd186human GRCh37 chr17: 18,241,329-18,241,638 , GRCh38.p12 chr17: 18,338,015-18,338,324 , GRCh38.p12 chr17|NW_017363819.1: 98,389-98,698 SHMT1
    nsv5974534inversion1nstd209human GRCh38 chr17: 15,750,079-18,634,890 , GRCh37.p13 chr17: 15,653,393-18,538,203 , ADORA2B, 119 more genes
    nsv5940881copy number variation1nstd209human GRCh38 chr17: 18,359,589-18,361,722 , GRCh37.p13 chr17: 18,262,903-18,265,036 SHMT1
    nsv5934241copy number variation1nstd209human GRCh38 chr17: 18,338,015-18,338,323 , GRCh37.p13 chr17: 18,241,329-18,241,637 SHMT1
    nsv5933579copy number variation1nstd209human GRCh38 chr17: 16,936,959-20,558,118 , GRCh37.p13 chr17: 16,840,273-20,461,431 , FAM106B, 146 more genes
    nsv5726484mobile element insertion2nstd211human GRCh38 chr17: 18,359,783-18,359,783 , GRCh37.p13 chr17: 18,263,097-18,263,097 SHMT1
    nsv5725147mobile element insertion1nstd211human GRCh38 chr17: 18,349,110-18,349,110 , GRCh37.p13 chr17: 18,252,424-18,252,424 SHMT1
    nsv5665112inversion1nstd207human GRCh37.p13 chr17: 16,704,599-18,417,421 , GRCh38 chr17: 16,801,285-18,514,107 , DRG2, 71 more genes
    nsv5645220insertion1nstd207human GRCh38 chr17: 18,359,694-18,359,694 , GRCh37.p13 chr17: 18,263,008-18,263,008 SHMT1
    nsv5563122mobile element insertion1nstd206human GRCh38 chr17: 18,359,733-18,359,783 , GRCh37.p13 chr17: 18,263,047-18,263,097 SHMT1
    nsv5545192insertion1nstd206human GRCh38 chr17: 18,355,712-18,355,726 , GRCh37.p13 chr17: 18,259,026-18,259,040 SHMT1
    nsv5531178copy number variation1nstd206human GRCh38 chr17: 18,354,124-18,355,551 , GRCh37.p13 chr17: 18,257,438-18,258,865 SHMT1
    nsv5528831copy number variation1nstd206human GRCh38 chr17: 18,349,036-18,350,946 , GRCh37.p13 chr17: 18,252,350-18,254,260 SHMT1
    nsv5527369copy number variation1nstd206human GRCh38 chr17: 18,338,015-18,338,324 , GRCh37.p13 chr17: 18,241,329-18,241,638 SHMT1
    nsv5524477copy number variation1nstd206human GRCh38 chr17: 18,359,816-18,361,633 , GRCh37.p13 chr17: 18,263,130-18,264,947 SHMT1
    nsv5515278copy number variation1nstd206human GRCh38 chr17: 18,340,996-18,344,427 , GRCh37.p13 chr17: 18,244,310-18,247,741 MIR6778, SHMT1
    nsv5381800copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,601,603-20,063,369 , GRCh38.p12 chr17: 16,698,289-20,160,056 COTL1P1, LOC105371551, 141 more genes
    nsv5381797copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,145,361-20,137,943 , GRCh38.p12 chr17: 17,242,047-20,234,630 LOC644909, FLII, 117 more genes
    nsv5324461copy number variation1nstd204human GRCh38.p13 chr17: 18,359,857-18,361,641 , GRCh37.p13 chr17: 18,263,171-18,264,955 SHMT1
    nsv5308539copy number variation1nstd204human GRCh38.p13 chr17: 18,330,715-18,331,064 , GRCh37.p13 chr17: 18,234,029-18,234,378 SHMT1
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