DG-CST

NIH Genetic Testing Registry

MSY Breakpoint Mapper

Sequence-tagged sites in the human Y chromosome

HCAD - Human Chromosome Aberration Database

Chromosomal breakpoints and affected genes

NECTAR

Disease-related non-synonymous mutations

VarySysDB

Various types of human gene polymorphism

HGVS Databases

A compilation of human mutation databases

Gene Wiki

The goal of the Gene Wiki is to apply community intelligence to the annotation of gene and protein function. The Gene Wiki is an informal collection of pages on human genes and proteins, and this effo ...

PhenoModifier

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 ...

Genetics Home Reference

The Genetics Home Reference is designed for patients and others to learn about specific genetic conditions and the genes that cause them. While the research results from the Human Genome Project are i ...

GeneCards: human genes, protein and diseases

GeneCards is a searchable, integrated, database of human genes that provides concise genomic, transcriptomic, genetic, proteomic, functional and disease related information on all known and predicted ...

Cypriot national mutation database

Disease mutations in the Cypriot population

rVarbase

Annotated SNPs within regulatory DNA elements

dbPSHP

A database of recent positive selection across human populations

F-SNP

Functional effects of various human SNPs

GWAS Diagram Browser

VADE

VarySysDB Disease Edition: Disease-associated genomic polymorphisms

dbSAP

Single Amino acid polymorphisms: SNP-derived variation in human proteins

MutDB

The goal of MutDB is to annotate human variation data with protein structural information and other functionally relevant information, if available. The mutations are organized by gene. Click on the a ...

dbCRID

Database of Chromosomal Rearrangements In Diseases