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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054383inversion1nstd229human GRCh38 chr3: 136,184,622-136,819,800 , GRCh37.p13 chr3: 135,903,464-136,538,642 HMGN1P10, DNAJC8P2, 8 more genes
    nsv7052094inversion1nstd229human GRCh38 chr3: 132,609,279-139,052,095 , GRCh37.p13 chr3: 132,328,123-138,770,937 RNU6-789P, UBA5, 98 more genes
    nsv7051105inversion1nstd229human GRCh38 chr3: 135,822,556-136,310,727 , GRCh37.p13 chr3: 135,541,398-136,029,569 PCCB, DONSONP1, 6 more genes
    nsv7044513inversion1nstd229human GRCh38 chr3: 131,210,998-138,882,695 , GRCh37.p13 chr3: 130,929,842-138,601,537 HSPA8P9, RNU6-1174P, 114 more genes
    nsv7039302inversion1nstd229human GRCh38 chr3: 133,378,933-139,551,784 , GRCh37.p13 chr3: 133,097,777-139,270,626 ESYT3, DONSONP1, 99 more genes
    nsv7039034inversion1nstd229human GRCh38 chr3: 136,134,661-138,768,814 , GRCh37.p13 chr3: 135,853,503-138,487,656 KRT8P36, RPL31P23, 37 more genes
    nsv6736753copy number variation1nstd229human GRCh38 chr3: 136,134,601-136,184,600 , GRCh37.p13 chr3: 135,853,443-135,903,442 CRIPTOP6, PPP2R3A, 1 more genes
    nsv6726709copy number variation1nstd229human GRCh38 chr3: 136,163,365-136,166,171 , GRCh37.p13 chr3: 135,882,207-135,885,013 MSL2
    nsv6725357copy number variation1nstd229human GRCh38 chr3: 136,179,254-136,183,474 , GRCh37.p13 chr3: 135,898,096-135,902,316 MSL2
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6575239inversion1nstd223human GRCh38 chr3: 136,170,267-136,170,618 , GRCh37.p13 chr3: 135,889,109-135,889,460 MSL2
    nsv6573821inversion1nstd223human GRCh38 chr3: 136,159,383-136,160,285 , GRCh37.p13 chr3: 135,878,225-135,879,127 MSL2
    nsv6566725inversion1nstd223human GRCh38 chr3: 136,177,585-136,178,854 , GRCh37.p13 chr3: 135,896,427-135,897,696 MSL2
    nsv6560897inversion1nstd223human GRCh38 chr3: 136,184,622-136,819,803 , GRCh37.p13 chr3: 135,903,464-136,538,645 HMGN1P10, DNAJC8P2, 8 more genes
    nsv6371987copy number variation1nstd223human GRCh38 chr3: 136,181,698-136,184,382 , GRCh37.p13 chr3: 135,900,540-135,903,224 MSL2
    nsv6367050copy number variation1nstd223human GRCh38 chr3: 136,187,426-136,188,476 , GRCh37.p13 chr3: 135,906,268-135,907,318 MSL2
    nsv6364125copy number variation1nstd223human GRCh38 chr3: 136,181,025-136,181,791 , GRCh37.p13 chr3: 135,899,867-135,900,633 MSL2
    nsv6154241copy number variation1nstd214human GRCh38 chr3: 136,187,246-136,187,325 , GRCh37.p13 chr3: 135,906,088-135,906,167 MSL2
    nsv6134991copy number variation1nstd213human GRCh37 chr3: 135,380,000-136,070,001 , GRCh38.p12 chr3: 135,661,158-136,351,159 PCCB, PPP2R3A, 8 more genes
    nsv6134785copy number variation1nstd213human GRCh37 chr3: 135,840,000-139,360,001 , GRCh38.p12 chr3: 136,121,158-139,641,159 ACTG1P1, FOXL2, 59 more genes
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