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Items: 1 to 20 of 287

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098722copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 26,726,714-26,750,699 , GRCh38.p12 chr2: 26,503,846-26,527,831 OTOF
    nsv7096643copy number variation1nstd102humanUncertain significance GRCh37 chr2: 26,414,119-26,712,628 , GRCh38.p12 chr2: 26,191,250-26,489,760 HADHA, ADGRF3, 6 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
    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
    nsv6677501copy number variation1nstd229human GRCh38 chr2: 26,498,058-26,504,172 , GRCh37.p13 chr2: 26,720,926-26,727,040 OTOF
    nsv6674836copy number variation1nstd229human GRCh38 chr2: 26,525,554-26,543,846 , GRCh37.p13 chr2: 26,748,422-26,766,714 OTOF
    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
    nsv6670003copy number variation1nstd229human GRCh38 chr2: 26,442,406-26,578,191 , GRCh37.p13 chr2: 26,665,274-26,801,059 OTOF, CIMIP2C, 1 more genes
    nsv6669537copy number variation1nstd229human GRCh38 chr2: 26,494,085-26,496,923 , GRCh37.p13 chr2: 26,716,953-26,719,791 OTOF
    nsv6669062copy number variation1nstd229human GRCh38 chr2: 26,458,027-26,461,083 , GRCh37.p13 chr2: 26,680,895-26,683,951 OTOF
    nsv6668898copy number variation1nstd229human GRCh38 chr2: 26,530,107-26,532,432 , GRCh37.p13 chr2: 26,752,975-26,755,300 OTOF
    nsv6667500copy number variation1nstd229human GRCh38 chr2: 26,471,892-26,520,333 , GRCh37.p13 chr2: 26,694,760-26,743,201 OTOF
    nsv6665331copy number variation1nstd229human GRCh38 chr2: 26,500,201-26,503,000 , GRCh37.p13 chr2: 26,723,069-26,725,868 OTOF
    nsv6659992copy number variation1nstd229human GRCh38 chr2: 26,555,622-26,558,688 , GRCh37.p13 chr2: 26,778,490-26,781,556 OTOF
    nsv6659791copy number variation1nstd229human GRCh38 chr2: 26,447,801-26,458,500 , GRCh37.p13 chr2: 26,670,669-26,681,368 DRC1, OTOF
    nsv6658686copy number variation1nstd229human GRCh38 chr2: 26,504,684-26,567,917 , GRCh37.p13 chr2: 26,727,552-26,790,785 OTOF, CIMIP2C
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628045copy number variation1nstd224human GRCh37 chr2: 26,575,986-26,760,625 , GRCh38.p12 chr2: 26,353,118-26,537,757 OTOF, DRC1, 1 more genes
    nsv6627670copy number variation1nstd224human GRCh37 chr2: 26,778,413-26,818,167 , GRCh38.p12 chr2: 26,555,545-26,595,299 OTOF, CIMIP2C, 1 more genes
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