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Items: 1 to 20 of 87

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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
    nsv7076630inversion1nstd229human GRCh38 chr10: 29,313,096-30,347,685 , GRCh37.p13 chr10: 29,602,025-30,636,614 LOC105376475, RNU6-598P, 22 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
    nsv7058187inversion1nstd229human GRCh38 chr10: 27,002,297-30,809,591 , GRCh37.p13 chr10: 27,291,226-31,098,520 RNU6-490P, LOC105376474, 87 more genes
    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
    nsv6885429copy number variation1nstd229human GRCh38 chr10: 29,599,986-29,618,300 , GRCh37.p13 chr10: 29,888,915-29,907,229 SVIL, MIR938
    nsv6593310inversion1nstd223human GRCh38 chr10: 29,384,765-30,593,038 , GRCh37.p13 chr10: 29,673,694-30,881,967 LOC105376479, RN7SL63P, 30 more genes
    nsv6584945inversion1nstd223human GRCh38 chr10: 29,510,330-30,674,089 , GRCh37.p13 chr10: 29,799,259-30,963,018 LOC107984218, LOC102724333, 28 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
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6131782copy number variation1nstd213human GRCh37 chr10: 28,950,000-33,420,001 , GRCh38.p12 chr10: 28,661,071-33,131,073 CCND3P1, MAP3K8, 88 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
    nsv5126027mobile element insertion1nstd203human GRCh38 chr10: 29,600,834-29,600,844 , GRCh37.p13 chr10: 29,889,763-29,889,773 SVIL, MIR938
    nsv4983915copy number variation1nstd200human GRCh38 chr10: 29,599,986-29,618,300 , GRCh37.p13 chr10: 29,888,915-29,907,229 SVIL, MIR938
    nsv4833356copy number variation1nstd200human GRCh37 chr10: 29,888,915-29,907,229 , GRCh38.p12 chr10: 29,599,986-29,618,300 MIR938, SVIL
    nsv4680495copy number variation1nstd189human GRCh37.p13 chr10: 29,866,139-30,340,823 , GRCh38.p12 chr10: 29,577,210-30,051,894 SVIL, JCAD, 9 more genes
    nsv4674851copy number variation1nstd102humanUncertain significance GRCh37 chr10: 29,204,926-30,604,037 , GRCh38.p12 chr10: 28,915,997-30,315,108 EEF1A1P39, LOC107984173, 25 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
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