LovD Platform
Our Data on LovD platform
Brazilian Molecular Database on Craniofacial Anomalies is the genotype of 253 variants in 41 genes, with 358 Healthy individuals with no history of oral clefting in the past three generations, and 157 patients with Non-syndromic Cleft Lip and Palate.
Click hereThe BRCA Challenge of the Global Alliance for Genomics and Health (GA4GH) aims to advance understanding of the genetic basis of breast cancer and related cancers by pooling data on BRCA genetic variants from around the world, bringing together information on sequence variation and clinical features in diverse populations. Our node show variants found in the Brazilian population
Click hereBrazilian Variants Database.
Click hereList of mutations found in Brazilian patients with Neurofibromatosis, NF1/NF2 genes sequencing, using Sanger sequencing.
Click hereList of mutations found in Brazilian patients with Tuberous Sclerosis, sequencing of TSC1 and TSC2 genes, using Sanger sequencing.
Click hereThe database design follows the recommendations of the Human Genome Variation Society, in addition to the principles and guidelines of the [Global Alliance for Genomics and Health (GA4GH)](http://genomicsandhealth.org/) for the ethical and responsible sharing of genomic and clinical information.