Patient: P_clcad2_test Analysis: A_clcad2_test Change filter settings Label Select all Select default Select none Benign Likely benign Likely pathogenic Pathogenic Variant of unknown significance Unlabeled Array design CI Array Design Not specified Type Select all Select none Homozygous deletion Deletion Normal Duplication Multiplication Loss of heterzygosity Chromosomal location Source Show all Manual bluegnome.xls Apply filter Reset filter
