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Clinical Trials on Copy Number Variations

Total 2689 results

NCT04561440

Unknown

Copy Number Variation in Prenatal Diagnosis

Copy Number Variation | Genome
NCT04774640

Terminated

Development of a NIPTT for Detecting Copy Number Variations

Copy Number Variations
NCT04191226

Recruiting

Genetic Mutation in Recurrent Cervical Cancer

Microsatellite Instability | Recurrent Cervical Cancer | PD-L1 | Nucleotide Variant | Copy Number Variation | Insertion-deletion Variation | Genomic Structural Variation | Total Mutation Burden | PD-1
NCT04191252

Recruiting

Genetic Mutation in Epithelial Ovarian Cancer

Epithelial Ovarian Cancer | Microsatellite Instability | PD-L1 | Nucleotide Variant | Copy Number Variation | Insertion-deletion Variation | Genomic Structural Variation | Total Mutation Burden | PD-1
NCT04285814

Completed

Technology Development for Noninvasive Prenatal Genetic Diagnosis Using Whole Fetal Cells from Maternal Peripheral Blood

Genetic Disease | Prenatal Diagnosis | Copy Number Abnormality

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