MPG Primer: Clinical interpretation of genes and variants for disease causality (2022)

(1:2:23)

Introduction to Genomic Variant Interpretation for Clinicians

(5:15)

Evaluating the Clinical Significance of Cytogenomic Variants

(22:2)

Why Clinicians Should Learn About Variant Interpretation

(8:40)

Not All Gene Changes Are the Same: Variants of Unknown Clinical Significance

(3:48)

Understanding clinical variability for variants in the same gene

(36:44)

Panel 2: Consistency of Interpretation of Variants Across Expert Labs/Groups, ClinVar Submissions

(20:1econd)

The NCBI Minute: Find All Variants with ClinVar

(9:54)

PATS Webinar - Clinical Genetics #2

(1:29:44)

Clinical Variant Interpretation, Dr. Brian Shirts

(53:54)

Elaine Lyon - Clinical Interpretation of Sequence Variants

(59:39)

Mapping Legacy Variants to HGVS

(21:3)

MPG Primer: Clinical Variant and Gene Classification (2023)

(49:14)

Clinical Interpretation of Genomic Variants - What we need to keep in mind - Dr. Vinod Scaria

(30:47)

MPG Primer: Clinical interpretation of sequence variants (2017)

(54:30)

Using clinically validated variants in assessing NGS technologies

(11:20)

Common risk variants and complex disorders

(32:3)

Using ClinVar to Share Germline \u0026 Somatic Variant Classifications from Clinical Genomic Testing

(59:15)

GM4: NHGRI Clinically Relevant Genomic Variants Initiatives - Erin Ramos

(26:23)