Learn about the current and future initiatives of the International Collaboration for Clinical Genomics (ICCG)! As part of our commitment to data sharing and collaboration to improve patient care, ICCG is creating a universal, clinical-grade database of genomic variation (including structural and sequence variants), available to the public through resources such as NCBI’s ClinVar database, and much more.
"I have previously used Alamut Visual in the UK and it is an invaluable resource for variant curation which I was keen to bring into use in my new role in New Zealand. provides a convenient and user-friendly interface which pulls together literature searches, population databases and in silico prediction tools. This enables streamlining of the curation process and saves a lot of time."
Wellington Regional Genetics Laboratory, Wellington, New Zealand