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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115852copy number variation1nstd186human GRCh37 chr16: 22,452,321-22,467,807 , GRCh38.p12 chr16: 22,441,000-22,456,486 , GRCh38.p12 chr16|NW_017852933.1: 648,549-664,040 SMG1P1
    nsv6114680copy number variation1nstd186human GRCh37 chr16: 22,503,807-22,710,621 , GRCh38.p12 chr16: 22,492,486-22,699,300 SMG1P1, OTOAP1, 3 more genes
    nsv6113913copy number variation1nstd186human GRCh37 chr16: 22,488,171-22,493,321 , GRCh38.p12 chr16: 22,476,850-22,482,000 SMG1P1
    nsv5980457copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 21,936,726-22,461,225 , GRCh38.p12 chr16: 21,925,405-22,449,904 , GRCh38.p12 chr16|NW_017852933.1: 655,131-1,179,634 CDR2, UQCRC2, 16 more genes
    nsv5971279inversion1nstd209human GRCh38 chr16: 21,590,269-22,770,846 , GRCh37.p13 chr16: 21,601,590-22,782,167 CDR2, UQCRC2, 31 more genes
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5929387copy number variation1nstd209human GRCh38 chr16: 20,698,055-24,692,430 , GRCh37.p13 chr16: 20,709,377-24,703,751 , ACSM1, 87 more genes
    nsv5700164mobile element insertion1nstd211human GRCh38 chr16: 22,457,395-22,457,395 , GRCh37.p13 chr16: 22,468,716-22,468,716 SMG1P1
    nsv5696885mobile element insertion1nstd211human GRCh38 chr16: 22,463,574-22,463,574 , GRCh37.p13 chr16: 22,474,895-22,474,895 SMG1P1
    nsv5662025insertion1nstd207human GRCh38 chr16: 22,462,643-22,462,643 , GRCh37.p13 chr16: 22,473,964-22,473,964 SMG1P1
    nsv5649670insertion1nstd207human GRCh38 chr16: 22,457,759-22,457,759 , GRCh37.p13 chr16: 22,469,080-22,469,080 SMG1P1
    nsv5594746copy number variation1nstd207human GRCh38 chr16: 22,479,524-22,479,945 , GRCh37.p13 chr16: 22,490,845-22,491,266 SMG1P1
    nsv5592710copy number variation1nstd207human GRCh38 chr16: 22,469,247-22,469,461 , GRCh37.p13 chr16: 22,480,568-22,480,782 SMG1P1
    nsv5592178copy number variation1nstd207human GRCh38 chr16: 22,436,053-22,436,739 , GRCh37.p13 chr16: 22,447,374-22,448,060 SMG1P1, RRN3P3
    nsv5591545copy number variation1nstd207human GRCh38 chr16: 22,479,834-22,479,957 , GRCh37.p13 chr16: 22,491,155-22,491,278 SMG1P1
    nsv5531854copy number variation1nstd206human GRCh38 chr16: 22,416,486-22,438,486 , GRCh37.p13 chr16: 22,427,807-22,449,807 RRN3P3, SMG1P1
    nsv5531837copy number variation1nstd206human GRCh38 chr16: 22,427,624-22,436,804 , GRCh37.p13 chr16: 22,438,945-22,448,125 RRN3P3, SMG1P1
    nsv5422584copy number variation1nstd206human GRCh38 chr16: 22,476,850-22,482,000 , GRCh37.p13 chr16: 22,488,171-22,493,321 SMG1P1
    nsv5422279copy number variation1nstd206human GRCh38 chr16: 22,441,000-22,456,486 , GRCh37.p13 chr16: 22,452,321-22,467,807 SMG1P1
    nsv5419610copy number variation1nstd206human GRCh38 chr16: 22,492,486-22,699,300 , GRCh37.p13 chr16: 22,503,807-22,710,621 SMG1P1, NPIPB5, 3 more genes
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