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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077900inversion1nstd229human GRCh38 chr14: 82,348,366-87,667,930 , GRCh37.p13 chr14: 82,814,710-88,134,274 LINC02301, LINC02305, 25 more genes
    nsv7071644inversion1nstd229human GRCh38 chr14: 86,450,775-87,093,880 , GRCh37.p13 chr14: 86,917,119-87,560,224 LINC01148, LOC105370608
    nsv7069334inversion1nstd229human GRCh38 chr14: 84,501,002-89,358,377 , GRCh37.p13 chr14: 84,967,346-89,824,721 EML5, LOC105370612, 35 more genes
    nsv7066414inversion1nstd229human GRCh38 chr14: 79,890,342-89,436,638 , GRCh37.p13 chr14: 80,356,685-89,902,982 SPATA7, RNU6ATAC28P, 82 more genes
    nsv7063507inversion1nstd229human GRCh38 chr14: 86,911,865-86,916,811 , GRCh37.p13 chr14: 87,378,209-87,383,155 LINC01148
    nsv6974449copy number variation1nstd229human GRCh38 chr14: 86,897,961-86,932,783 , GRCh37.p13 chr14: 87,364,305-87,399,127 LINC01148
    nsv6971312copy number variation1nstd229human GRCh38 chr14: 86,865,558-87,146,948 , GRCh37.p13 chr14: 87,331,902-87,613,292 LOC105370608, LINC01148
    nsv6967862copy number variation1nstd229human GRCh38 chr14: 86,902,520-87,002,451 , GRCh37.p13 chr14: 87,368,864-87,468,795 LINC01148
    nsv6964830copy number variation1nstd229human GRCh38 chr14: 86,908,866-86,914,464 , GRCh37.p13 chr14: 87,375,210-87,380,808 LINC01148
    nsv6963733copy number variation1nstd229human GRCh38 chr14: 86,917,916-86,918,753 , GRCh37.p13 chr14: 87,384,260-87,385,097 LINC01148
    nsv6963040copy number variation1nstd229human GRCh38 chr14: 86,912,359-86,914,794 , GRCh37.p13 chr14: 87,378,703-87,381,138 LINC01148
    nsv6962662copy number variation1nstd229human GRCh38 chr14: 86,707,995-87,031,285 , GRCh37.p13 chr14: 87,174,339-87,497,629 LINC01148
    nsv6962178copy number variation1nstd229human GRCh38 chr14: 86,890,417-86,908,797 , GRCh37.p13 chr14: 87,356,761-87,375,141 LINC01148
    nsv6637996copy number variation1nstd102humanUncertain significance GRCh37 chr14: 85,366,999-90,760,040 , GRCh38.p12 chr14: 84,900,655-90,293,696 LOC105370608, FOXN3-AS2, 49 more genes
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
    nsv6637462copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 81,593,708-97,059,276 , GRCh38.p12 chr14: 81,127,364-96,592,939 SERPINA3, BDKRB1, 210 more genes
    nsv6592963inversion1nstd223human GRCh38 chr14: 86,486,184-95,139,000 , GRCh37.p13 chr14: 86,952,528-95,605,337 CCDC88C-DT, RPSAP4, 134 more genes
    nsv6495249copy number variation1nstd223human GRCh38 chr14: 86,919,931-87,008,882 , GRCh37.p13 chr14: 87,386,275-87,475,226 LINC01148
    nsv6492876copy number variation1nstd223human GRCh38 chr14: 86,903,600-86,905,728 , GRCh37.p13 chr14: 87,369,944-87,372,072 LINC01148
    nsv6488745copy number variation1nstd223human GRCh38 chr14: 86,919,472-86,920,113 , GRCh37.p13 chr14: 87,385,816-87,386,457 LINC01148
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