• 1. Database of Genomic Variants
• A comprehensive summary of structural variation in the human genome.

• 2. Gene Reviews
• GeneReviews are expert-authored, peer-reviewed, current disease descriptions that apply genetic testing to the diagnosis, management, and genetic counseling of patients and families with specific inhe

• 3. GeneCards
• GeneCards is an integrated database of human genes that includes automatically-mined genomic, proteomic and transcriptomic information, as well as orthologies, disease relationships, SNPs, gene expression, gene function, and service links for ordering assays and antibodies.

• 4. GeneTests
• Managed by the NIH, GeneTests provides publicly funded medical genetics information resource developed for physicians, other healthcare providers, and researchers.

• 5. GeneTests' Gene Reviews - GeneClinics
• GeneReviews are expert-authored, peer-reviewed, current disease descriptions that apply genetic testing to the diagnosis, management, and genetic counseling of patients and families with specific inherited conditions. Many genetic counselors use Gene Reviews every day.

• 6. Genetic Testing Registry (GTR)
• GTR replaces GeneTests from the NCBI. It provides details on genetic tests: test's purpose, methodology, validity, evidence of the test's usefulness, and laboratory contacts and credentials.

• 7. Genetics databases
• CDC maintained list of genetic databases

• 8. Genetics Home Reference
• National Library of Medicine resource for genetic information targeted toward the public

• 9. Metabolic and molecular bases of inherited disease
• E-book of molecular mechanisms of disease and inheritance

• 10. OMIM
• Online Mendelian Inheritance in Man (OMIM) is a continuously updated catalog of human genes and genetic disorders. OMIM focuses primarily on inherited, or heritable, genetic diseases. It is also considered to be a phenotypic companion to the human genome project.

• 11. The Online Metabolic and Molecular Bases of Inherited Disease
• OMMBID provides the latest knowledge on the molecular and metabolic underpinnings of a growing list of inherited diseases, as well as updates on pathophysiology and treatment.