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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098853copy number variation1nstd102humanUncertain significance GRCh37 chr2: 24,962,301-26,257,604 , GRCh38.p12 chr2: 24,739,432-26,034,735 TPM3P7, EFR3B, 25 more genes
    nsv7096625copy number variation1nstd102humanUncertain significance GRCh37 chr2: 24,443,763-30,143,525 , GRCh38.p12 chr2: 24,220,894-29,920,659 LOC105374381, POMC, 136 more genes
    nsv7096411copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,443,763-26,029,226 , GRCh38.p12 chr2: 24,220,894-25,806,357 LOC105369164, DTNB-AS1, 24 more genes
    nsv7096148copy number variation2nstd102humanUncertain significance GRCh37 chr2: 24,443,763-29,022,169 , GRCh38.p12 chr2: 24,220,894-28,799,303 LOC105374381, SLC35F6, 122 more genes
    nsv6675821copy number variation1nstd229human GRCh38 chr2: 24,710,616-24,914,385 , GRCh37.p13 chr2: 24,933,485-25,137,254 PTRHD1, CENPO, 4 more genes
    nsv6674629copy number variation1nstd229human GRCh38 chr2: 24,323,879-25,622,192 , GRCh37.p13 chr2: 24,546,748-25,845,061 POMC, RNA5SP88, 22 more genes
    nsv6673927copy number variation1nstd229human GRCh38 chr2: 24,444,134-24,913,408 , GRCh37.p13 chr2: 24,667,003-25,136,277 LOC105369164, CENPO, 7 more genes
    nsv6673034copy number variation1nstd229human GRCh38 chr2: 24,858,165-24,858,213 , GRCh37.p13 chr2: 25,081,034-25,081,082 ADCY3
    nsv6672785copy number variation1nstd229human GRCh38 chr2: 24,384,939-32,866,867 , GRCh37.p13 chr2: 24,607,808-33,091,934 CENPO, TOGARAM2, 170 more genes
    nsv6672457copy number variation1nstd229human GRCh38 chr2: 24,817,381-24,821,398 , GRCh37.p13 chr2: 25,040,250-25,044,267 CENPO, ADCY3
    nsv6672447copy number variation1nstd229human GRCh38 chr2: 24,757,901-24,942,900 , GRCh37.p13 chr2: 24,980,770-25,165,769 PTRHD1, CENPO, 5 more genes
    nsv6671906copy number variation1nstd229human GRCh38 chr2: 24,915,379-24,919,263 , GRCh37.p13 chr2: 25,138,248-25,142,132 ADCY3
    nsv6670543copy number variation1nstd229human GRCh38 chr2: 24,899,339-24,901,701 , GRCh37.p13 chr2: 25,122,208-25,124,570 ADCY3
    nsv6669231copy number variation1nstd229human GRCh38 chr2: 24,865,507-24,865,536 , GRCh37.p13 chr2: 25,088,376-25,088,405 ADCY3
    nsv6669027copy number variation1nstd229human GRCh38 chr2: 24,856,290-25,101,000 , GRCh37.p13 chr2: 25,079,159-25,323,869 ADCY3, RN7SL856P, 5 more genes
    nsv6668086copy number variation1nstd229human GRCh38 chr2: 24,906,222-24,906,262 , GRCh37.p13 chr2: 25,129,091-25,129,131 ADCY3
    nsv6667661copy number variation1nstd229human GRCh38 chr2: 24,897,518-24,914,124 , GRCh37.p13 chr2: 25,120,387-25,136,993 ADCY3
    nsv6667018copy number variation1nstd229human GRCh38 chr2: 24,818,453-24,818,529 , GRCh37.p13 chr2: 25,041,322-25,041,398 CENPO, ADCY3
    nsv6665399copy number variation1nstd229human GRCh38 chr2: 24,873,002-24,959,588 , GRCh37.p13 chr2: 25,095,871-25,182,457 ADCY3, DNAJC27
    nsv6665287copy number variation1nstd229human GRCh38 chr2: 24,819,766-24,819,864 , GRCh37.p13 chr2: 25,042,635-25,042,733 CENPO, ADCY3
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