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New ClinVar graphical display - NCBI Insights
ClinVar Archives - NCBI Insights
IJMS | Free Full-Text | Aggregated Genomic Data as Cohort-Specific Allelic Frequencies can Boost Variants and Genes Prioritization in Non-Solved Cases of Inherited Retinal Dystrophies
![PDF] ClinVar: improving access to variant interpretations and supporting evidence | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/128ba335c95595ea6846fed1c349601e97a18e5e/2-Figure1-1.png "PDF] ClinVar: improving access to variant interpretations and supporting evidence | Semantic Scholar")
PDF] ClinVar: improving access to variant interpretations and supporting evidence | Semantic Scholar
IJMS | Free Full-Text | A Comprehensive Evaluation of the Performance of Prediction Algorithms on Clinically Relevant Missense Variants
Assessment of an automated approach for variant interpretation in screening for monogenic disorders: A single‐center study - Gall - Molecular Genetics & Genomic Medicine - Wiley Online Library
New ClinVar graphical display - NCBI Insights
What is ClinVar? A database for variant interpretation! [Today's pape…
New ClinVar graphical display - NCBI Insights
CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer | Nature Genetics
Using ClinVar as a Resource to Support Variant Interpretation. - Abstract - Europe PMC
Clinical laboratories collaborate to resolve differences in variant interpretations submitted to ClinVar | Genetics in Medicine
Genome Alert!: a standardized procedure for genomic variant reinterpretation and automated genotype-phenotype reassessment in clinical routine | medRxiv
New ClinVar graphical display - NCBI Insights
Frontiers | Mastermind: A Comprehensive Genomic Association Search Engine for Empirical Evidence Curation and Genetic Variant Interpretation
![PDF] ClinVar: public archive of relationships among sequence variation and human phenotype | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/ed95339eb652c67570cd2b0093a2758b8139e9e1/2-Table1-1.png "PDF] ClinVar: public archive of relationships among sequence variation and human phenotype | Semantic Scholar")
PDF] ClinVar: public archive of relationships among sequence variation and human phenotype | Semantic Scholar
Genes | Free Full-Text | Annotation of Human Exome Gene Variants with Consensus Pathogenicity
ClinVar - ClinGen | Clinical Genome Resource
A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer | Nature Genetics
New ClinVar graphical display - NCBI Insights
![PDF] Clinotator: analyzing ClinVar variation reports to prioritize reclassification efforts | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/a7c0e187c02501c23bc0ac6fa66512fd0cb1c655/4-Table1-1.png "PDF] Clinotator: analyzing ClinVar variation reports to prioritize reclassification efforts | Semantic Scholar")
PDF] Clinotator: analyzing ClinVar variation reports to prioritize reclassification efforts | Semantic Scholar
![PDF] ClinVar: public archive of interpretations of clinically relevant variants | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/a77e1886e8d8659f89c6dfacbbf339cb3c5c0672/4-Figure2-1.png "PDF] ClinVar: public archive of interpretations of clinically relevant variants | Semantic Scholar")
PDF] ClinVar: public archive of interpretations of clinically relevant variants | Semantic Scholar
ClinVar: public archive of interpretations of clinically relevant variants
