Introduction to Genomic Variant Curation For Clinicians
Are you new to the process of genomic variant interpretation? ClinGen is producing a series of webinars walking new users through points to consider and resources available. In this short introductory video, we explain how understanding this information may be of benefit to those in clinical practice.
Evaluating the Clinical Significance of Copy Number Variants - Points to Consider
This webinar walks the user through the general process of classifying structural variants, and describes key information to consider when evaluating these types of variants.
ClinGen Dosage Sensitivity Map
One of the resources that ClinGen provides is our Dosage Sensitivity Map. Learn how we evaluate genes and genomic regions for dosage sensitivity, and how to access the data for your own use.
Learn more about how ClinGen is partnering with individuals to advance genomic medicine through GenomeConnect, our patient portal.
The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. If you have questions about the information contained on this website, please see a health care professional.