e.g. AMT | PLA2G6 | Pachygyria
Data Policy
The Indian Variant Database (INDVar) is an India-centric platform designed to archive, manage, and share clinically relevant genomic variants, particularly rare disease-associated variants and Variants of Uncertain Significance (VOUS). INDVar enables seamless collaboration between clinicians, diagnostic laboratories, and researchers to support variant discovery, clinical interpretation, and functional validation. By contributing data, users agree to follow INDVar standards for data quality, privacy, ethical sharing, and scientific attribution.
Open Access: Publicly shareable variant-level data, gene associations, and OMIM disease information are available for research use.
Managed Access: Sensitive clinical or unpublished functional data may remain under controlled access or embargo.
Permitted Use: Academic research, variant interpretation, functional genomics, diagnostics, and educational purposes.
Restricted Use: Patient re-identification, unauthorized redistribution, and commercial reuse without approval.
No direct identifiers: such as patient names or phone numbers, will be disclosed, and the information will be used solely for research purposes, not for any diagnostic use.
Security: The system provides role-based access control and secure login sessions.
- GRCh37 / GRCh38 coordinates
- ACMG classification
- HPO phenotype terms
- OMIM disease mapping
INDVar connects clinicians with research laboratories capable of validating VOUS and novel variants.