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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5715918mobile element insertion2nstd211human GRCh38 chr7: 44,405,547-44,405,547 , GRCh37.p13 chr7: 44,445,146-44,445,146 NUDCD3
    nsv5561273mobile element insertion1nstd206human GRCh38 chr7: 44,405,561-44,405,598 , GRCh37.p13 chr7: 44,445,160-44,445,197 NUDCD3
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5490606copy number variation1nstd206human GRCh38 chr7: 44,480,549-44,480,678 , GRCh37.p13 chr7: 44,520,148-44,520,277 NUDCD3
    nsv5484952copy number variation1nstd206human GRCh38 chr7: 44,454,110-44,454,655 , GRCh37.p13 chr7: 44,493,709-44,494,254 NUDCD3
    nsv5484456copy number variation1nstd206human GRCh38 chr7: 44,434,226-44,434,284 , GRCh37.p13 chr7: 44,473,825-44,473,883 NUDCD3
    nsv5477624copy number variation1nstd206human GRCh38 chr7: 44,377,915-44,379,919 , GRCh37.p13 chr7: 44,417,514-44,419,518 NUDCD3
    nsv5477225copy number variation1nstd206human GRCh38 chr7: 44,428,721-44,428,800 , GRCh37.p13 chr7: 44,468,320-44,468,399 NUDCD3
    nsv5476790copy number variation1nstd206human GRCh38 chr7: 44,405,101-44,408,883 , GRCh37.p13 chr7: 44,444,700-44,448,482 NUDCD3
    nsv5381787copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,341,583-50,171,623 , GRCh38.p12 chr7: 43,301,984-50,132,027 OGDH, LOC112267918, 110 more genes
    nsv5381783copy number variation1nstd102humanPathogenic GRCh37 chr7: 41,124,364-47,945,566 , GRCh38.p12 chr7: 41,084,766-47,905,969 ELK1P1, URGCP, 121 more genes
    nsv5378735translocation1nstd200human GRCh38 chr7: 44,379,919-44,379,919 , GRCh38 chr7: 44,377,915-44,377,915 , GRCh37.p13 chr7: 44,417,514-44,417,514 , GRCh37.p13 chr7: 44,419,518-44,419,518 NUDCD3
    nsv5368189translocation1nstd200human GRCh38 chr5: 39,793,860-39,793,860 , GRCh38 chr7: 44,469,101-44,469,101 , GRCh37.p13 chr7: 44,508,700-44,508,700 , GRCh37.p13 chr5: 39,793,962-39,793,962 NUDCD3
    nsv5343613translocation1nstd200human GRCh37 chr7: 44,448,482-44,448,482 , GRCh37 chr7: 44,444,700-44,444,700 , GRCh38.p12 chr7: 44,408,883-44,408,883 , GRCh38.p12 chr7: 44,405,101-44,405,101 NUDCD3
    nsv5329720translocation1nstd200human GRCh37 chr7: 44,417,514-44,417,514 , GRCh37 chr7: 44,419,518-44,419,518 , GRCh38.p12 chr7: 44,379,919-44,379,919 , GRCh38.p12 chr7: 44,377,915-44,377,915 NUDCD3
    nsv5306811copy number variation1nstd204human GRCh38.p13 chr7: 44,405,097-44,408,884 , GRCh37.p13 chr7: 44,444,696-44,448,483 NUDCD3
    nsv5233694copy number variation1nstd204human GRCh38.p13 chr7: 44,405,201-44,408,900 , GRCh37.p13 chr7: 44,444,800-44,448,499 NUDCD3
    nsv5229262copy number variation1nstd204human GRCh38.p13 chr7: 44,405,285-44,408,884 , GRCh37.p13 chr7: 44,444,884-44,448,483 NUDCD3
    nsv5220667copy number variation1nstd204human GRCh38.p13 chr7: 44,454,627-44,457,232 , GRCh37.p13 chr7: 44,494,226-44,496,831 NUDCD3
    nsv5197321mobile element insertion1nstd203human GRCh38 chr7: 44,405,547-44,405,561 , GRCh37.p13 chr7: 44,445,146-44,445,160 NUDCD3
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