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Items: 1 to 20 of 121

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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
    nsv7070202inversion1nstd229human GRCh38 chr10: 27,330,033-30,802,827 , GRCh37.p13 chr10: 27,618,962-31,091,756 LINC00837, RPL21P93, 77 more genes
    nsv7067182inversion1nstd229human GRCh38 chr10: 28,478,269-28,585,774 , GRCh37.p13 chr10: 28,767,198-28,874,703 WAC-AS1, LINC02652, 1 more genes
    nsv7058187inversion1nstd229human GRCh38 chr10: 27,002,297-30,809,591 , GRCh37.p13 chr10: 27,291,226-31,098,520 RNU6-490P, LOC105376474, 87 more genes
    nsv6896517copy number variation1nstd229human GRCh38 chr10: 28,343,471-28,533,887 , GRCh37.p13 chr10: 28,632,400-28,822,816 LOC107984216, WAC, 4 more genes
    nsv6896048copy number variation1nstd229human GRCh38 chr10: 28,528,501-28,534,400 , GRCh37.p13 chr10: 28,817,430-28,823,329 WAC, WAC-AS1
    nsv6894377copy number variation1nstd229human GRCh38 chr10: 28,466,728-36,061,502 , GRCh37.p13 chr10: 28,755,657-36,350,430 LOC105376482, LOC101929431, 130 more genes
    nsv6892132copy number variation1nstd229human GRCh38 chr10: 28,369,351-28,574,320 , GRCh37.p13 chr10: 28,658,280-28,863,249 LINC02652, WAC, 4 more genes
    nsv6582027inversion1nstd223human GRCh38 chr10: 26,903,422-36,846,484 , GRCh37.p13 chr10: 27,192,351-37,135,412 KIF5B, EPC1-AS1, 167 more genes
    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
    nsv6291211copy number variation1nstd102humanPathogenic GRCh37 chr10: 27,204,530-29,105,882 , GRCh38.p12 chr10: 26,915,601-28,816,953 LINC02673, FAM210CP, 44 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
    nsv6131781copy number variation1nstd213human GRCh37 chr10: 28,800,000-29,040,001 , GRCh38.p12 chr10: 28,511,071-28,751,072 BAMBI, WAC, 7 more genes
    nsv5914382copy number variation1nstd209human GRCh38 chr10: 27,312,316-36,846,398 , GRCh37.p13 chr10: 27,601,245-37,135,326 , RN7SL241P, 160 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4182287copy number variation1nstd166human GRCh37.p13 chr10: 28,818,206-28,820,843 , GRCh38.p12 chr10: 28,529,277-28,531,914 WAC, WAC-AS1
    nsv4180848copy number variation1nstd166human GRCh37.p13 chr10: 28,811,790-28,815,880 , GRCh38.p12 chr10: 28,522,861-28,526,951 WAC-AS1
    nsv3921533copy number variation1nstd102humanPathogenic GRCh37 chr10: 28,056,899-30,335,014 , NCBI36 chr10: 28,096,905-30,375,020 , GRCh38 chr10: 27,767,970-30,046,085 ODAD2, LOC107984170, 48 more genes
    nsv3920796copy number variation1nstd102humanPathogenic NCBI36 chr10: 62,842-35,729,127 , GRCh37.p13 chr10: 72,842-35,689,121 , GRCh38.p12 chr10: 26,906-35,400,193 EPC1-AS1, RNU6-452P, 559 more genes
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