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Items: 1 to 20 of 137

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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
    nsv7074105inversion1nstd229human GRCh38 chr10: 17,945,641-22,801,235 , GRCh37.p13 chr10: 18,252,931-23,090,164 UBE2V2P1, LOC105376450, 62 more genes
    nsv7061293inversion1nstd229human GRCh38 chr10: 18,677,449-18,677,569 , GRCh37.p13 chr10: 18,966,378-18,966,498 ARL5B
    nsv6888370copy number variation1nstd229human GRCh38 chr10: 18,680,812-18,743,991 , GRCh37.p13 chr10: 18,969,741-19,032,920 AIFM1P1, ARL5B, 1 more genes
    nsv6888094copy number variation1nstd229human GRCh38 chr10: 18,656,701-18,665,700 , GRCh37.p13 chr10: 18,945,630-18,954,629 NSUN6, ARL5B
    nsv6881493copy number variation1nstd229human GRCh38 chr10: 18,226,684-19,178,310 , GRCh37.p13 chr10: 18,515,613-19,467,239 LOC107984213, CACNB2, 8 more genes
    nsv6878896copy number variation1nstd229human GRCh38 chr10: 18,659,953-18,660,130 , GRCh37.p13 chr10: 18,948,882-18,949,059 ARL5B
    nsv6637959copy number variation1nstd102humanUncertain significance GRCh37 chr10: 18,969,812-19,032,885 , GRCh38.p12 chr10: 18,680,883-18,743,956 AIFM1P1, LOC105376440, 1 more genes
    nsv6635502copy number variation1nstd227human GRCh38.p12 chr10: 18,493,951-19,380,438 , GRCh37 chr10: 18,782,880-19,669,367 CACNB2, NSUN6, 7 more genes
    nsv6593934inversion1nstd223human GRCh38 chr10: 18,668,850-18,669,640 , GRCh37.p13 chr10: 18,957,779-18,958,569 ARL5B
    nsv6576985inversion1nstd223human GRCh38 chr10: 18,670,413-18,671,254 , GRCh37.p13 chr10: 18,959,342-18,960,183 ARL5B
    nsv6443757copy number variation1nstd223human GRCh38 chr10: 18,647,752-18,704,055 , GRCh37.p13 chr10: 18,936,681-18,992,984 NSUN6, ARL5B
    nsv6439814copy number variation1nstd223human GRCh38 chr10: 18,681,392-18,682,116 , GRCh37.p13 chr10: 18,970,321-18,971,045 ARL5B
    nsv6439355copy number variation1nstd223human GRCh38 chr10: 18,661,437-18,662,060 , GRCh37.p13 chr10: 18,950,366-18,950,989 ARL5B
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6132031copy number variation1nstd213human GRCh37 chr10: 18,100,000-28,260,001 , GRCh38.p12 chr10: 17,839,748-27,971,072 BMI1, CACNB2, 136 more genes
    nsv5364780translocation1nstd200human GRCh38 chr10: 18,678,205-18,678,205 , GRCh38 chr10: 98,754,746-98,754,746 , GRCh37.p13 chr10: 100,514,503-100,514,503 , GRCh37.p13 chr10: 18,967,134-18,967,134 ARL5B, HPSE2
    nsv5128429mobile element insertion1nstd203human GRCh38 chr10: 18,663,041-18,663,062 , GRCh37.p13 chr10: 18,951,970-18,951,991 ARL5B
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