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

• 2. dbGaP
• The database of Genotype and Phenotype (dbGaP) was developed to archive and distribute the results of studies that have investigated the interaction of genotype and phenotype. Such studies include genome-wide association studies, medical sequencing, molecular diagnostic assays, as well as association between genotype and non-clinical traits.

• 3. ENCODE Project at UCSC
• Browser and portal for NHGRI's ENCODE project. This is the official repository of sequence-related data for the ENCODE Consortium and supports the coordination of data submission, storage, retrieval, and visualization.

• 4. 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.

• 5. Genome Browsers and Tools Resource List
• Galter Library-created list of genome browsers and genome analysis servers

• 6. Genome Variation Server
• The Genome Variation Server (GVS) is a local database hosted by the SeattleSNPs Program for Genomic Applications (PGA). The objective of this database is to provide a simple tool for rapid access to human genotype data found in dbSNP, and to provide tools for analysis of genotype data.

• 7. HGMD®: Human Genome Mutation Database
• The HGMD is a comprehensive listing of gene mutations. Users must register for the most current version, which is free to academic users.

• 8. HGVbaseG2P: a Human Genome Variation and Genotype/Phenotype Database
• The Human Genome Variation database of Genotype-to-Phenotype information (HGVbaseG2P) provides a centralized compilation of summary level findings from genetic association studies, both large and small. They actively gather datasets from public domain projects, and encourage direct data submission from the community.

• 9. National Human Genome Research Institute | genome.gov |
• The NHGRI is the home organization for the Human Genome Project and a source of a great deal of information on genomics and genetic research

• 10. NUgene Project
• NUGene collects and stores DNA samples along with healthcare information from patients of Northwestern-affiliated hospitals and clinics. This resource is made available to scientists for research purposes.

• 11. 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.