ClinVar Reaches One Million Variants!

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(Audio Described Version) ClinVar Reaches One Million Variants!

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The NCBI Minute: Find All Variants with ClinVar

(9:54)

How to Search ClinVar

(8:51)

Using ClinVar: what it is, why it matters, and how to incorporate it into your variant reviews

(12:41)

Understanding Variant Interpretation Discrepancy in ClinVar [Part 1]

(5:9)

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

(20:1econd)

Clinvar

(6:37)

ClinVar Miner

(34:46)

ANNOVAR How to annotate genetic variants

(26:29)

MPG Primer: Clinical Variant and Gene Classification (2023)

(49:14)

Presentation - Intro to Genome Analysis (Christina Austin-Tse)

(43:44)

HGVS nomenclature basics and legacy variants

(59:17)

Presentation - Use of the Genome Aggregation Database (gnomAD) (Anne O'Donnell-Luria)

(43:12)

Introduction to Variants and Nomenclature

(12:49)

NCBI dbSNP and dbVar

(20:46)

Accurate Variant Classification and Clinical Impact of variability (2023) - webinar 3

(1:31:1econd)

Annotating your own variation data with the Ensembl Variant Effect Predictor VEP

(57:43)

Variants of Uncertain Significance

(5:50)

Webinar: MedGen, GTR, and Clinvar

(42:12)

ClinVar Data: Current Limitations for Germline Variants | Center for Genomic Interpretation | Oct'23

(23:10)

Using ClinVar - For the ClinGen Biocurator Working Group

(45:43)

Presentation - Use of and Submission to ClinVar (Melissa Landrum)

(39:46)

GenomeConnect and ClinVar Webinar

(45:38)

Using Mastermind’s New ClinVar Integration to Accelerate Clinical Diagnoses

(1:23)

ClinGen and ClinVar: Complementary resources - Erin Riggs

(19:20)

Understanding Variant Interpretation Discrepancy in ClinVar [Part 2]

(11:29)

Navigating the ClinVar Database

(58:18)

ClinVar 10th Anniversary

(1:21)