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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977843inversion1nstd209human GRCh37.p13 chr3: 38,198,806-38,332,023 , GRCh38 chr3: 38,157,315-38,290,532 SLC22A14, SLC22A13, 3 more genes
    nsv5967080insertion1nstd209human GRCh38 chr3: 38,212,101-38,212,101 , GRCh37.p13 chr3: 38,253,592-38,253,592 OXSR1
    nsv5716428mobile element insertion1nstd211human GRCh38 chr3: 38,254,731-38,254,731 , GRCh37.p13 chr3: 38,296,222-38,296,222 OXSR1
    nsv5714611mobile element insertion2nstd211human GRCh38 chr3: 38,212,116-38,212,116 , GRCh37.p13 chr3: 38,253,607-38,253,607 OXSR1
    nsv5445221copy number variation1nstd206human GRCh38 chr3: 38,247,919-38,248,184 , GRCh37.p13 chr3: 38,289,410-38,289,675 OXSR1
    nsv5443345copy number variation1nstd206human GRCh38 chr3: 38,235,425-38,235,482 , GRCh37.p13 chr3: 38,276,916-38,276,973 OXSR1
    nsv5436749copy number variation1nstd206human GRCh38 chr3: 38,169,182-38,169,267 , GRCh37.p13 chr3: 38,210,673-38,210,758 OXSR1
    nsv5177014mobile element insertion1nstd203human GRCh38 chr3: 38,212,101-38,212,116 , GRCh37.p13 chr3: 38,253,592-38,253,607 OXSR1
    nsv5174063mobile element insertion1nstd203human GRCh38 chr3: 38,212,100-38,212,116 , GRCh37.p13 chr3: 38,253,591-38,253,607 OXSR1
    nsv5162553mobile element insertion1nstd203human GRCh38 chr3: 38,212,106-38,212,116 , GRCh37.p13 chr3: 38,253,597-38,253,607 OXSR1
    nsv5069917mobile element insertion1nstd203human GRCh38 chr3: 38,214,241-38,214,257 , GRCh37.p13 chr3: 38,255,732-38,255,748 OXSR1
    nsv5068205mobile element insertion1nstd203human GRCh38 chr3: 38,184,951-38,184,951 , GRCh37.p13 chr3: 38,226,442-38,226,442 OXSR1
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5032429inversion1nstd200human GRCh38 chr3: 38,157,315-38,290,531 , GRCh37.p13 chr3: 38,198,806-38,332,022 SLC22A14, SLC22A13, 3 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4924338copy number variation1nstd200human GRCh38 chr3: 38,224,858-38,230,509 , GRCh37.p13 chr3: 38,266,349-38,272,000 OXSR1
    nsv4910842copy number variation1nstd200human GRCh38 chr3: 38,247,919-38,248,184 , GRCh37.p13 chr3: 38,289,410-38,289,675 OXSR1
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4888484inversion1nstd200human GRCh37 chr3: 38,198,806-38,332,022 , GRCh38.p12 chr3: 38,157,315-38,290,531 SLC22A14, SLC22A13, 3 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
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