GenTIGSA Gene Database on Rare Genetic Disorders
  Beta Version

Lists of Rare Genetic Disorders  

Common Variable Immune Deficiency      Explore Disorder's Alias
An Autosomal dominant, Autosomal recessive mode(s) within the Immune disorders category
Reported Pathogenic variants
Candidate Gene Information
S.No. Name/GeneID Description Cytogentic Band Gene Location on genomic DNA Gene Length Exons Details Gene Cross-References
1 CD19/930 CD19 molecule 16p11.2 Chr16, NC_000016.10
(28931971..28939342)
7372 nt 14 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

2 TNFRSF13B/23495 TNF receptor superfamily member 13B 17p11.2 Chr17, NC_000017.11
(16939081..16972118, complement)
33038 nt 5 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

3 TNFRSF13C/115650 TNF receptor superfamily member 13C 22q13.2 Chr22, NC_000022.11
(41922032..41926806, complement)
4775 nt 3 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

Variant Information
Disorder Cross-References:      GARD          GTR          MalaCards          NORD     

Patient care services
Clinical Symptoms & Disabilities

Prevalence
Under development