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Items: 1 to 20 of 240

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077330inversion1nstd229human GRCh38 chr21: 20,333,755-29,497,356 , GRCh37.p13 chr21: 21,706,067-30,869,676 LOC105372770, LOC100419737, 95 more genes
    nsv7076627inversion1nstd229human GRCh38 chr21: 28,020,569-28,108,480 , GRCh37.p13 chr21: 29,392,888-29,480,799 LINC01697, LINC00314
    nsv7076620inversion1nstd229human GRCh38 chr21: 26,722,526-28,250,115 , GRCh37.p13 chr21: 28,094,845-29,622,434 LINC00113, LOC102724355, 14 more genes
    nsv7071358inversion1nstd229human GRCh38 chr21: 23,691,748-31,155,798 , GRCh37.p13 chr21: 25,064,065-32,528,116 LLPHP2, KRTAP20-3, 126 more genes
    nsv7066381inversion1nstd229human GRCh38 chr21: 28,015,154-28,015,169 , GRCh37.p13 chr21: 29,387,473-29,387,488 LINC00314
    nsv7066097inversion1nstd229human GRCh38 chr21: 24,633,921-28,114,599 , GRCh37.p13 chr21: 26,006,235-29,486,918 ADAMTS5, MARCKSP1, 43 more genes
    nsv7065590inversion1nstd229human GRCh38 chr21: 23,756,613-30,931,318 , GRCh37.p13 chr21: 25,128,930-32,303,637 LINC01697, LOC105372753, 119 more genes
    nsv7031312copy number variation1nstd229human GRCh38 chr21: 27,937,883-28,033,978 , GRCh37.p13 chr21: 29,310,202-29,406,297 LINC00314
    nsv7023945copy number variation1nstd229human GRCh38 chr21: 27,856,301-31,095,924 , GRCh37.p13 chr21: 29,228,620-32,468,242 KRTAP19-11P, KRTAP6-2, 78 more genes
    nsv7022043copy number variation1nstd229human GRCh38 chr21: 27,578,449-28,037,795 , GRCh37.p13 chr21: 28,950,768-29,410,114 LINC01673, LINC00314, 1 more genes
    nsv7021583copy number variation1nstd229human GRCh38 chr21: 26,860,401-28,609,800 , GRCh37.p13 chr21: 28,232,720-29,982,122 LINC01695, MIR4759, 15 more genes
    nsv7019281copy number variation1nstd229human GRCh38 chr21: 26,864,834-28,052,292 , GRCh37.p13 chr21: 28,237,153-29,424,611 LINC00314, LINC00113, 12 more genes
    nsv6637343copy number variation1nstd102humanUncertain significance GRCh37 chr21: 29,243,314-32,472,073 , GRCh38.p12 chr21: 27,870,995-31,099,755 GAPDHP14, LINC00189, 78 more genes
    nsv6626624copy number variation1nstd224human GRCh37 chr21: 1-48,129,895 , GRCh38.p12 chr21: 8,522,361-46,699,983 , ATP5PO, 657 more genes
    nsv6598206inversion1nstd223human GRCh38 chr21: 28,020,375-28,021,054 , GRCh37.p13 chr21: 29,392,694-29,393,373 LINC00314
    nsv6549449copy number variation1nstd223human GRCh38 chr21: 26,864,834-28,052,292 , GRCh37.p13 chr21: 28,237,153-29,424,611 LOC105372762, LOC102724355, 12 more genes
    nsv6315551copy number variation1nstd102humanPathogenic GRCh37 chr21: 14,420,615-48,080,926 , GRCh38.p12 chr21: 13,048,294-46,661,014 LTN1, LOC105372740, 622 more genes
    nsv6314196copy number variation1nstd102humanUncertain significance GRCh37 chr21: 27,185,913-35,853,445 , GRCh38.p12 chr21: 25,813,602-34,481,147 RPL12P9, CLDN17, 173 more genes
    nsv6313951copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,041,209-48,097,372 , GRCh38.p12 chr21: 13,668,888-46,677,460 LOC107985515, ATP5PF, 606 more genes
    nsv6291465copy number variation1nstd102humanLikely benign GRCh37 chr21: 28,240,161-29,421,743 , GRCh38.p12 chr21: 26,867,842-28,049,424 LOC102724355, LOC105372759, 12 more genes
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