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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5902118copy number variation1nstd209human GRCh38 chr4: 67,515,180-67,517,595 , GRCh37.p13 chr4: 68,380,898-68,383,313 CENPC
    nsv5900748copy number variation1nstd209human GRCh38 chr4: 67,487,225-67,488,268 , GRCh37.p13 chr4: 68,352,943-68,353,986 CENPC
    nsv5839763copy number variation1nstd209human GRCh38 chr4: 67,487,238-67,488,237 , GRCh37.p13 chr4: 68,352,956-68,353,955 CENPC
    nsv5839456copy number variation1nstd209human GRCh38 chr4: 67,515,221-67,517,654 , GRCh37.p13 chr4: 68,380,939-68,383,372 CENPC
    nsv5685800mobile element insertion1nstd211human GRCh38 chr4: 67,541,253-67,541,253 , GRCh37.p13 chr4: 68,406,971-68,406,971 CENPC
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5613921insertion1nstd207human GRCh38 chr4: 67,491,468-67,491,468 , GRCh37.p13 chr4: 68,357,186-68,357,186 CENPC
    nsv5577712copy number variation1nstd207human GRCh38 chr4: 67,487,225-67,488,268 , GRCh37.p13 chr4: 68,352,943-68,353,986 CENPC
    nsv5553228insertion1nstd206human GRCh38 chr4: 67,541,097-67,541,132 , GRCh37.p13 chr4: 68,406,815-68,406,850 CENPC
    nsv5473832copy number variation1nstd206human GRCh38 chr4: 67,515,188-67,517,596 , GRCh37.p13 chr4: 68,380,906-68,383,314 CENPC
    nsv5472277copy number variation1nstd206human GRCh38 chr4: 67,374,723-67,478,420 , GRCh37.p13 chr4: 68,240,441-68,344,138 RNU1-63P, CENPC, 2 more genes
    nsv5470197copy number variation1nstd206human GRCh38 chr4: 67,487,227-67,488,269 , GRCh37.p13 chr4: 68,352,945-68,353,987 CENPC
    nsv5466902copy number variation1nstd206human GRCh38 chr4: 67,532,169-67,532,859 , GRCh37.p13 chr4: 68,397,887-68,398,577 CENPC
    nsv5461393copy number variation1nstd206human GRCh38 chr4: 67,494,569-67,494,727 , GRCh37.p13 chr4: 68,360,287-68,360,445 CENPC
    nsv5456336copy number variation1nstd206human GRCh38 chr4: 67,511,384-67,511,843 , GRCh37.p13 chr4: 68,377,102-68,377,561 CENPC
    nsv5410330mobile element insertion1nstd206human GRCh38 chr4: 67,541,253-67,541,304 , GRCh37.p13 chr4: 68,406,971-68,407,022 CENPC
    nsv5389416copy number variation2nstd186human GRCh37 chr4: 68,380,906-68,383,314 , GRCh38.p12 chr4: 67,515,188-67,517,596 CENPC
    nsv5317972copy number variation1nstd204human GRCh38.p13 chr4: 67,487,217-67,488,278 , GRCh37.p13 chr4: 68,352,935-68,353,996 CENPC
    nsv5308022copy number variation1nstd204human GRCh38.p13 chr4: 67,515,164-67,517,618 , GRCh37.p13 chr4: 68,380,882-68,383,336 CENPC
    nsv5236208copy number variation1nstd204human GRCh38.p13 chr4: 67,515,705-67,517,579 , GRCh37.p13 chr4: 68,381,423-68,383,297 CENPC
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