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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5864276copy number variation1nstd209human GRCh38 chr10: 38,460,295-38,463,749 , GRCh37.p13 chr10: 38,749,223-38,752,677 SEPTIN14P10
    nsv5588677copy number variation1nstd207human GRCh38 chr10: 38,460,241-38,461,188 , GRCh37.p13 chr10: 38,749,169-38,750,116 SEPTIN14P10
    nsv5258134copy number variation1nstd204human GRCh38.p13 chr10: 38,460,245-38,463,749 , GRCh37.p13 chr10: 38,749,173-38,752,677 SEPTIN14P10
    nsv5244242copy number variation1nstd204human GRCh38.p13 chr10: 38,460,201-38,461,100 , GRCh37.p13 chr10: 38,749,129-38,750,028 SEPTIN14P10
    nsv5242403copy number variation1nstd204human GRCh38.p13 chr10: 38,456,401-38,463,800 , GRCh37.p13 chr10: 38,745,329-38,752,728 SEPTIN14P10
    nsv5035636inversion1nstd200human GRCh38 chr10: 32,580,256-50,959,654 , GRCh37.p13 chr10: 32,869,184-52,719,414 , ZNF32-AS2, 320 more genes
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4988775copy number variation1nstd200human GRCh38 chr10: 38,305,317-38,826,633 , GRCh37.p13 chr10: 38,594,245-39,119,764 , HSD17B7P2, 12 more genes
    nsv4986280copy number variation1nstd200human GRCh38 chr10: 38,460,038-38,463,819 , GRCh37.p13 chr10: 38,748,966-38,752,747 SEPTIN14P10
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4676011copy number variation1nstd102humanLikely benign GRCh37 chr10: 38,064,033-38,900,673 , GRCh38.p12 chr10: 37,775,105-38,607,542 EIF3LP3, CCNYL4, 20 more genes
    nsv4675921copy number variation1nstd102humanLikely benign GRCh37 chr10: 37,189,335-38,900,673 , GRCh38.p12 chr10: 36,900,407-38,607,542 ZNF248, RNU6-1118P, 38 more genes
    nsv4671818copy number variation1nstd186human GRCh37 chr10: 38,726,639-38,877,388 , GRCh38.p12 chr10: 38,437,711-38,584,257 , LINC00999, 2 more genes
    nsv4667969copy number variation1nstd186human GRCh37 chr10: 38,749,168-38,752,704 , GRCh38.p12 chr10: 38,460,240-38,463,776 SEPTIN14P10
    nsv4666981copy number variation2nstd186human GRCh37 chr10: 38,701,624-39,132,382 , GRCh38.p12 chr10: 38,412,696-38,839,251 , ACTR3BP5, 9 more genes
    nsv4654017copy number variation1nstd186human GRCh37 chr10: 38,749,125-38,752,663 , GRCh38.p12 chr10: 38,460,197-38,463,735 SEPTIN14P10
    nsv4647403copy number variation1nstd186human GRCh37 chr10: 38,749,169-38,752,704 , GRCh38.p12 chr10: 38,460,241-38,463,776 SEPTIN14P10
    nsv4608236copy number variation1nstd183human GRCh37 chr10: 38,693,727-38,771,531 , GRCh38.p12 chr10: 38,404,799-38,482,603 , LINC00999, 4 more genes
    nsv4607891copy number variation1nstd183human GRCh37 chr10: 38,749,168-38,752,704 , GRCh38.p12 chr10: 38,460,240-38,463,776 SEPTIN14P10
    nsv4606597copy number variation2nstd183human GRCh37 chr10: 38,726,639-38,877,388 , GRCh38.p12 chr10: 38,437,711-38,584,257 , CICP9, 2 more genes
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