Other names: canvas
CanVaS is a Greek cancer patient genetic variation resource.
genotype and phenotype genetic variation oncology pathology exome sequencing
An ethnic-specific database of Indian germline variants.
A database of somatic mutations in normal human tissues.
NHLBI Exome Sequencing Project (ESP): Exome Variant Server (EVS) for browsing single nucleotide variation data from exome sequencing experiments mainly focused on heart, lung and blood disorders.
An Evidence-based Database of Genes and Phenotypes of Male Infertility.
The Human Genetic Variation Database (HGVD) aims to provide a central resource to archive and display Japanese genetic variation and association between the variation and transcription level of genes. ...
A Resource for Mapping Variants onto Experimental and Modeled Structures of Human Protein Complexes.
an integrated database and analytic platform for de novo mutations in humans. De novo mutations (DNMs) significantly contribute to sporadic diseases, particularly in neuropsychiatric disorders. Whole ...
Genotype-Tissue Expression (GTEx) - database which helps to study the relationship between genetic variation and gene expression in human tissues.
The Exome Aggregation Consortium (ExAC) is a coalition of investigators seeking to aggregate and harmonize exome sequencing data from a variety of large-scale sequencing projects, and to make summary ...
An Integrated Genetic Database for Hearing Loss.
The European Variation Archive is an open-access archive that accepts submission of, and provides access to, all types of genetic variation data from all species. All users are able to download any da ...
PhenoModifier is a genetic modifier database for elucidating the genetic basis of human phenotypic variation. PhenoModifier provides a more complete spectrum of genetic factors contributing to human p ...
PharmGKB is a resource that provides information about how human genetic variation affects response to medications. PharmGKB collects, curates and disseminates knowledge about clinically actionable ge ...
Domestic Animal Diversity Information System is a communication and information tool for implementing strategies for the management of animal genetic resources. It provides the user with searchable da ...
A generic integrated web-based workflow system to evaluate genotype-phenotype correlations in human mitochondrial diseases.
Review and classification of published variants in the ARSB gene. The purpose of this database is to support researchers and clinicians. understand structural changes on alylsulfatase B (ASB) caused ...
CPRD GOLD linked Cancer Patient Experience Survey (CPES) data on initial GP visit, through diagnosis/treatment, to the ongoing management of cancer. Note, these data are no longer routinely available; ...
CPRD Aurum linked Cancer Patient Experience Survey (CPES) data on initial GP visit, through diagnosis/treatment, to the ongoing management of cancer. Note, these data are no longer routinely available ...
Genome Aggregation Database (gnomAD) - browser that aggregates exome and whole-genome sequencing data from a wide variety of large-scale sequencing projects. It enables search of genetic variation inf ...
Genetic mutation database for rare diseases that enables to search, sort and filter genetic variants from clinically diagnosed individuals worldwide and make symptoms-based queries.