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Items: 1 to 20 of 353

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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
    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
    nsv7066138inversion1nstd229human GRCh38 chr21: 22,253,885-27,921,241 , GRCh37.p13 chr21: 23,626,205-29,293,560 LOC107985516, D21S2088E, 57 more genes
    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
    nsv7059690inversion1nstd229human GRCh38 chr21: 26,938,907-26,938,948 , GRCh37.p13 chr21: 28,311,226-28,311,267 ADAMTS5
    nsv7036624copy number variation1nstd229human GRCh38 chr21: 26,945,201-26,955,300 , GRCh37.p13 chr21: 28,317,520-28,327,619 MIR4759, ADAMTS5
    nsv7034464copy number variation1nstd229human GRCh38 chr21: 26,926,701-26,930,100 , GRCh37.p13 chr21: 28,299,020-28,302,419 ADAMTS5
    nsv7032393copy number variation1nstd229human GRCh38 chr21: 26,917,776-27,322,823 , GRCh37.p13 chr21: 28,290,095-28,695,142 LOC105372759, LOC102724355, 3 more genes
    nsv7028994copy number variation1nstd229human GRCh38 chr21: 26,915,067-26,929,552 , GRCh37.p13 chr21: 28,287,386-28,301,871 ADAMTS5
    nsv7027594copy number variation1nstd229human GRCh38 chr21: 26,943,958-26,944,531 , GRCh37.p13 chr21: 28,316,277-28,316,850 ADAMTS5
    nsv7025623copy number variation1nstd229human GRCh38 chr21: 26,926,663-26,930,110 , GRCh37.p13 chr21: 28,298,982-28,302,429 ADAMTS5
    nsv7024458copy number variation1nstd229human GRCh38 chr21: 26,951,501-27,314,400 , GRCh37.p13 chr21: 28,323,820-28,686,719 MIR4759, ADAMTS5, 3 more genes
    nsv7021808copy number variation1nstd229human GRCh38 chr21: 26,392,260-27,183,788 , GRCh37.p13 chr21: 27,764,579-28,556,107 LOC107985474, MIR4759, 8 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
    nsv6635933copy number variation1nstd227human GRCh38.p12 chr21: 26,887,792-27,175,497 , GRCh37 chr21: 28,260,111-28,547,816 GPX1P2, ADAMTS5, 3 more genes
    nsv6634469copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,006,457-29,046,428 , GRCh38.p12 chr21: 13,634,136-27,674,109 ADAMTS5, VN2R20P, 160 more genes
    nsv6626865copy number variation1nstd224human GRCh37 chr21: 28,327,495-28,392,015 , GRCh38.p12 chr21: 26,955,176-27,019,696 ADAMTS5
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