NEXTflex® Targeted NGS Hybridization Panel 1 - This Targeted NGS Hybridization Panel 1 simplifies the identification of relevant single nucleotide variants (SNVs), small insertion and deletions (indels), and copy number variants (CNVs) in more than 75 genes related to endocrine and metabolic disorders, hemoglobinopathies, and primary immunodeficiencies.