Explore and integrate genomic variation, function and phenotypes
The IGVF Catalog serves as a centralized portal for datasets, annotations, experimental results and computational predictions from the IGVF Consortium, integrating data from sources such as ENCODE, MaveDB, and more.
Search for a variant, region, or gene
IGVF Catalog Apps
Catalog Apps, e.g. Coding, Disease-focused KP, etc.
FAVOR
Functional Annotation of Variants Online Resource
MaveDB
Database for MAVE experiments
Lipids Knowledge Portal
Lipids knowledge portal network
E2G
View enhancer-gene predictions from ENCODE, IGVF, and other projects
RegulomeDB
Tool to prioritize functionally important SNVs located within non-coding regions of the human genome
IGVF Coding Variants
Coding Variants Database
Explore the API
Access IGVF Consortium datasets programmatically through our comprehensive API, enabling seamless integration of genomic variation and functional data into your research workflows.
Documentation
Access detailed documentation and examples demonstrating how to query, visualize, and integrate IGVF resources. Future updates will expand use cases and API coverage.
IGVF Chatbot
The IGVF Chatbot assists users by translating natural language queries into AQL, retrieving results directly from our knowledge graph.