HGVS (Human Genome Variation Society) is a renowned brand dedicated to advancing genomic research and understanding. Their mission is to facilitate the discovery and characterization of genomic variations, including their population distribution and phenotypic associations. Through the collection, documentation, and free distribution of genomic variation information, HGVS aims to provide valuable resources for molecular diagnosis, research on basic mechanisms, and the design of treatments for human ailments.

As part of their efforts, HGVS offers various databases, including central mutation and SNP databases, disease-centered mutation databases, locus-specific mutation databases, and chromosomal and mitochondrial variation databases. These databases serve as comprehensive references for researchers, clinicians, and patients alike. HGVS also provides education resources and organizes meetings and conferences to promote collaboration and knowledge exchange among experts in the field.

Members of the Human Genome Variation Society can further benefit from a reduced subscription to the society's journal, Human Mutation. With a commitment to enhancing human health, HGVS is at the forefront of genomic research and its practical applications