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Items: 1 to 20 of 150

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7073007inversion1nstd229human GRCh38 chr10: 83,678,437-92,070,274 , GRCh37.p13 chr10: 85,438,193-93,830,031 PPP1R3C, LOC105378415, 157 more genes
    nsv7065381inversion1nstd229human GRCh38 chr10: 83,674,811-92,070,275 , GRCh37.p13 chr10: 85,434,567-93,830,032 LINC01520, RPS27P1, 158 more genes
    nsv6897098copy number variation1nstd229human GRCh38 chr10: 89,715,984-89,964,412 , GRCh37.p13 chr10: 91,475,741-91,724,169 MARK2P16, LOC105378424, 5 more genes
    nsv6894302copy number variation1nstd229human GRCh38 chr10: 89,808,883-90,278,470 , GRCh37.p13 chr10: 91,568,640-92,038,227 LINC01375, LOC105378424, 6 more genes
    nsv6893901copy number variation1nstd229human GRCh38 chr10: 89,825,685-89,963,919 , GRCh37.p13 chr10: 91,585,442-91,723,676 LOC105378424, MARK2P16, 3 more genes
    nsv6893892copy number variation1nstd229human GRCh38 chr10: 89,838,641-89,838,763 , GRCh37.p13 chr10: 91,598,398-91,598,520 LINC00865, MARK2P16
    nsv6887646copy number variation1nstd229human GRCh38 chr10: 89,829,484-89,834,300 , GRCh37.p13 chr10: 91,589,241-91,594,057 LOC105378424, LINC00865
    nsv6881928copy number variation1nstd229human GRCh38 chr10: 89,840,368-89,852,580 , GRCh37.p13 chr10: 91,600,125-91,612,337 LINC00865, LINC01374
    nsv6637868copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,823,147-96,056,941 , GRCh38.p12 chr10: 88,063,390-94,297,184 RPS27P1, RNLS, 118 more genes
    nsv6637857copy number variation1nstd102humanUncertain significance GRCh37 chr10: 91,478,772-91,725,006 , GRCh38.p12 chr10: 89,719,015-89,965,249 KIF20B, LINC01375, 5 more genes
    nsv6637542copy number variation1nstd102humanPathogenic GRCh37 chr10: 82,595,472-93,542,416 , GRCh38.p12 chr10: 80,835,716-91,782,659 IFIT6P, HECTD2, 166 more genes
    nsv6634458copy number variation1nstd102humanPathogenic GRCh37 chr10: 83,533,660-91,913,077 , GRCh38.p12 chr10: 81,773,904-90,153,320 IFIT5, IFIT1, 140 more genes
    nsv6585420inversion1nstd223human GRCh38 chr10: 89,833,967-89,834,938 , GRCh37.p13 chr10: 91,593,724-91,594,695 LINC00865
    nsv6449264copy number variation1nstd223human GRCh38 chr10: 89,827,291-89,832,497 , GRCh37.p13 chr10: 91,587,048-91,592,254 LINC00865, LOC105378424
    nsv6448916copy number variation1nstd223human GRCh38 chr10: 89,808,883-90,278,467 , GRCh37.p13 chr10: 91,568,640-92,038,224 SNRPD2P1, LINC00865, 6 more genes
    nsv6445163copy number variation1nstd223human GRCh38 chr10: 89,829,484-89,834,296 , GRCh37.p13 chr10: 91,589,241-91,594,053 LOC105378424, LINC00865
    nsv6436714copy number variation1nstd223human GRCh38 chr10: 89,833,822-89,835,780 , GRCh37.p13 chr10: 91,593,579-91,595,537 LINC00865
    nsv6131983copy number variation1nstd213human GRCh37 chr10: 91,480,000-91,730,001 , GRCh38.p12 chr10: 89,720,243-89,970,244 KIF20B, LINC00865, 5 more genes
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