NSGC’s Webinar Series is a timely, year-round series program focused on education and other issues impacting our profession. From telemedicine to genetic engineering, these webinars keep you apprised of how the latest trends in healthcare may affect you.
2026 Webinar Series Package
Get access to all 24 webinars, along with CEUs, from NSGC's 2026 Webinar Series in one comprehensive package.
Member price: $400
Non-member price: $475
Purchase 2026 Webinar Series
Purchase Individual Webinars
Browse and purchase individual webinars and their corresponding CEUs. Please note that while active NSGC members may access webinar recordings at no cost, CEUs require a purchase.
Member price: $35
Non-member price: $50
February 4: The future is here: Genome Sequencing as the first line prenatal diagnostic testing
Presented by: Prenatal SIG
Learning Objectives:
- Examine the value of genome sequencing in prenatal diagnosis as a single-tier, comprehensive test for all patients
- Assess benefits and limitations of different sequencing consenting and reporting strategies
- Explore the future state of non-invasive exome/genome sequencing
- Discuss the value of community and data sharing to move the field of prenatal diagnosis forward
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February 18: Practice Recommendations for Genetic Testing of Ataxias
Presented by: Neurogenetics SIG
Learning Objectives:
- Describe the rationale for creating standardized genetic testing recommendations
- Review the process for developing evidence-based, consensus driven guidelines
- Recommend an approach for evaluation and counseling for patients with a personal and/or family history ataxia
- Discuss considerations for test selection and associated methodologies
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March 18: Case Based Webinar - Part One
Presented by: Kendra Schaa, ScM, CGC Laura Godfrey Hendon, MA, MS, LCGC Rozalia Valentine, MS, CGC Brettne Frewin Elizabeth Spitzer, PhD
Learning Objectives:
- Illustrate the role of a genetic counselor in client-centered decision-making
- Demonstrate how genetic counselors fit within the larger healthcare system
- Review the wide differential and one center’s testing strategy for fetal cystic hygroma
- Examine the impact of severe intrafamilial variable expressivity in a “lethal” Mendelian disorder on patient expectations and coping
- Assess the limitations of current NMD vs NDD classification frameworks in DYNC1H1-related disorders and their impact on accurate diagnostic prognostication
- Integrate patient and caregiver narratives into genetic counseling practice to inform communication, expectation-setting, and support
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