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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5729911mobile element insertion1nstd211human GRCh38 chr10: 95,644,320-95,644,320 , GRCh37.p13 chr10: 97,404,077-97,404,077 ALDH18A1
    nsv5706797mobile element insertion2nstd211human GRCh38 chr10: 95,627,237-95,627,237 , GRCh37.p13 chr10: 97,386,994-97,386,994 ALDH18A1
    nsv5594866copy number variation1nstd207human GRCh38 chr10: 95,647,108-95,677,060 , GRCh37.p13 chr10: 97,406,865-97,436,817 ALDH18A1, TCTN3
    nsv5564286copy number variation1nstd102humanUncertain significance GRCh37 chr10: 97,366,499-98,031,175 , GRCh38.p12 chr10: 95,606,742-96,271,418 CCNJ, ENTPD1-AS1, 10 more genes
    nsv5561349sequence alteration1nstd206human GRCh38 chr10: 95,609,934-95,609,934 , GRCh37.p13 chr10: 97,369,691-97,369,691 ALDH18A1
    nsv5554180mobile element insertion1nstd206human GRCh38 chr10: 95,644,320-95,644,371 , GRCh37.p13 chr10: 97,404,077-97,404,128 ALDH18A1
    nsv5549497insertion1nstd206human GRCh38 chr10: 95,627,232-95,627,264 , GRCh37.p13 chr10: 97,386,989-97,387,021 ALDH18A1
    nsv5535253insertion1nstd206human GRCh38 chr10: 95,609,930-95,609,930 , GRCh37.p13 chr10: 97,369,687-97,369,687 ALDH18A1
    nsv5492695copy number variation1nstd206human GRCh38 chr10: 95,647,108-95,677,058 , GRCh37.p13 chr10: 97,406,865-97,436,815 TCTN3, ALDH18A1
    nsv5400372mobile element insertion1nstd206human GRCh38 chr10: 95,627,237-95,627,288 , GRCh37.p13 chr10: 97,386,994-97,387,045 ALDH18A1
    nsv5396771mobile element insertion1nstd206human GRCh38 chr10: 95,627,187-95,627,213 , GRCh37.p13 chr10: 97,386,944-97,386,970 ALDH18A1
    nsv5348011translocation1nstd200human GRCh38 chr10: 95,645,582-95,645,582 , GRCh38 chr10: 95,645,654-95,645,654 , GRCh37.p13 chr10: 97,405,339-97,405,339 , GRCh37.p13 chr10: 97,405,411-97,405,411 ALDH18A1
    nsv5309212copy number variation1nstd204human GRCh37.p13 chr10: 97,406,835-97,436,837 , GRCh38.p13 chr10: 95,647,078-95,677,080 ALDH18A1, TCTN3
    nsv5253641copy number variation1nstd204human GRCh38.p13 chr10: 95,648,377-95,650,276 , GRCh37.p13 chr10: 97,408,134-97,410,033 ALDH18A1
    nsv5245308copy number variation1nstd204human GRCh38.p13 chr10: 95,646,908-95,675,456 , GRCh37.p13 chr10: 97,406,665-97,435,213 ALDH18A1, TCTN3
    nsv5186499mobile element insertion1nstd203human GRCh38 chr10: 95,644,305-95,644,320 , GRCh37.p13 chr10: 97,404,062-97,404,077 ALDH18A1
    nsv5137981mobile element insertion1nstd203human GRCh38 chr10: 95,627,218-95,627,232 , GRCh37.p13 chr10: 97,386,975-97,386,989 ALDH18A1
    nsv5129957mobile element insertion1nstd203human GRCh38 chr10: 95,627,216-95,627,237 , GRCh37.p13 chr10: 97,386,973-97,386,994 ALDH18A1
    nsv5124905mobile element insertion1nstd203human GRCh38 chr10: 95,627,213-95,627,237 , GRCh37.p13 chr10: 97,386,970-97,386,994 ALDH18A1
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