|
LOVD v.3.0 - Leiden Open Variation Database
Online gene-centered collection and display of DNA variants
|
|
List of public LOVD installations
 |
If you are looking for a specific gene database, please also check our list of LSDBs. |
Please note that the latest available build is always installed on our Leiden server. We offer free use of this LOVD installation for those interested, e.g. to maintain/start a LSDB. Contact us for more information.
You can also download this list to see the complete list of genes in the databases.
| In total: 425,275 variants (201,275 unique) in 56,216 individuals in 37 LOVD installations. |
| http://proteomics.bio21.unimelb.edu.au/lovd/ |
LOVD 3.0-07 |
14772 genes |
239690 variants |
| LOVD - Leiden Open Variation Database |
A1BG,A1BG-AS1,A1CF,A2M,A2ML1,A4GALT,A4GNT,AAAS,AACS,AACSP... |
152241 unique |
| https://ab-openlab.csir.res.in/mitolsdb/ |
LOVD 2.0-35 |
37 genes |
112662 variants |
| MitoLSDB |
MTATP6,MTATP8,MTCO1,MTCO2,MTCO3,MTCYB,MTND1,MTND2,MTND3,M... |
4660 unique |
| http://HCI-LOVD.hci.utah.edu |
LOVD 2.0-33 |
8 genes |
26167 variants |
| LOVD - human mismatch repair genes |
MLH1,MLH1_priors,MSH2,MSH2_priors,MSH6,MSH6_priors,PMS2,P... |
26167 unique |
| https://grenada.lumc.nl/LOVD2/Usher_montpellier/ |
LOVD 2.0-37 |
20 genes |
23521 variants |
| Retinal and hearing impairment genetic mutation database |
CDH23,CEACAM16,CERKL,CHM,CLDN14,CLRN1,GPR98,MYO15A,MYO6,M... |
3656 unique |
| https://oi.gene.le.ac.uk/ |
LOVD 2.0-36 |
21 genes |
4901 variants |
| Osteogenesis Imperfecta Variant Database |
BMP1,CCDC134,COL1A1,COL1A2,CREB3L1,CRTAP,FAM46A,FKBP10,IF... |
2288 unique |
| http://rb1-lovd.d-lohmann.de/ |
LOVD 2.0-34 |
1 gene |
3397 variants |
| rb1-lsdb |
RB1 |
1753 unique |
| http://lovd.bx.psu.edu/ |
LOVD 2.0-38 |
37 genes |
2329 variants |
| The Globin Gene Server |
ALOX5AP,AQP9,ARG2,ASS1,ATRX,BCL11A,CNTNAP2,CSNK2A1,EPAS1,... |
2268 unique |
| https://eds.gene.le.ac.uk/ |
LOVD 2.0-36 |
13 genes |
2083 variants |
| Ehlers Danlos Syndrome Variant Database |
ADAMTS2,AEBP1,B3GALT6,B4GALT7,CHST14,COL3A1,COL5A1,COL5A2... |
1264 unique |
| http://lsdb.hgu.mrc.ac.uk/ |
LOVD 2.0-30 |
11 genes |
1903 variants |
| MRC Human Genetics Unit LOVD at MRC IGMM |
MLYCD,NIPBL,OTX2,PAX6,RAB18,RAB3GAP1,RAB3GAP2,RPGR,SMC1A,... |
1111 unique |
| http://hci-exlovd.hci.utah.edu/ |
LOVD 2.0-22 |
3 genes |
1822 variants |
| Database of BRCA1 and BRCA2 sequence variants that have been clinically reclassified using a quantit |
BRCA1,BRCA1fx,BRCA2 |
1850 unique |
| http://grenada.lumc.nl/LOVD2/VWF/ |
LOVD 2.0-37 |
1 gene |
1741 variants |
| EAHAD Coagulation Factor Variant Databases |
VWF |
715 unique |
| http://hgddatabase.cvtisr.sk/ |
LOVD 2.0-36 |
1 gene |
1220 variants |
| HGD mutation database |
HGD |
231 unique |
| http://mseqdr.lumc.edu/GEDI/ |
LOVD 3.0-08 |
298 genes |
1012 variants |
| The Genetic Eye Disorder (GEDI) Variation Database |
ABCA4,ABCC6,ABHD12,ADAM9,ADAMTS18,AFG3L1P,AHI1,AIP,AIPL1,... |
981 unique |
| http://143.169.238.105/LOVD/ |
LOVD 3.0-16 |
6 genes |
713 variants |
| Loeys-Dietz Syndrome Mutation Database |
SMAD2,SMAD3,TGFB2,TGFB3,TGFBR1,TGFBR2 |
328 unique |
| http://www.dbagenes.unito.it/ |
LOVD 2.0-36 |
13 genes |
399 variants |
| Diamond-Blackfan Anemia |
GATA1,RPL11,RPL15,RPL26,RPL31,RPL35A,RPL5,RPS10,RPS17,RPS... |
256 unique |
| http://dna2.leeds.ac.uk/LOVD/ |
LOVD 3.0-13 |
20 genes |
355 variants |
| LOVD - Leiden Open Variation Database |
ACPT,AMBN,AMELX,AMTN,C4orf26,COL17A1,DLX3,ENAM,FAM20A,FAM... |
228 unique |
| http://genome.igib.res.in/tblovd/ |
LOVD 2.0-20 |
71 genes |
341 variants |
| TBsLVD Tuberculosis susceptibility Locus Variation Database |
AKT1,ALOX5,BTNL2,CCL1,CCL2,CCL5,CD14,CD209,CHIT1,CISH,CR1... |
273 unique |
| http://fishmap2.igib.res.in/mirlovd/ |
LOVD 2.0-35 |
157 genes |
225 variants |
| miRvar |
MIR101_2,MIR10B,MIR1178,MIR1181,MIR1185_2,MIR1206,MIR1226... |
188 unique |
| https://lovd3.isciii.es/ |
LOVD 3.0-11 |
31 genes |
188 variants |
| SpainMDB |
ABCD1,APC,ATP7B,BRAF,BRCA1,BRCA2,BSND,CFTR,CYP27A1,DMD,GH... |
137 unique |
| https://drdb.gene.le.ac.uk/ |
LOVD 2.0-36 |
4 genes |
184 variants |
| Death Receptor Database (DRdb) |
TNFRSF10A,TNFRSF10B,TNFRSF10C,TNFRSF10D |
144 unique |
| http://www.genetik-regensburg.de/LOVDv.3.0/ |
LOVD 3.0-16 |
55 genes |
106 variants |
| Labor Staber Humangenetik |
ABCC8,AIP,ATM,ATP7B,ATXN3,BAP1,BLK,BRCA1,BRCA2,BRIP1,CDH1... |
101 unique |
| http://db.cshg.org.cy/ |
LOVD 3.0-17 |
44 genes |
86 variants |
| |
APC,APCS,ATP6V1B1,BRCA1,BRCA2,C1QA,C1QC,CFH,CFHR5,CFTR,CO... |
83 unique |
| http://dna2.leeds.ac.uk/GRK1_LOVD/ |
LOVD 3.0-18 |
1 gene |
69 variants |
| LOVD - Leiden Open Variation Database |
GRK1 |
28 unique |
| http://www.icp.ucl.ac.be/vikkula/CLPdb/ |
LOVD 2.0-36 |
1 gene |
54 variants |
| Cleft Lip and Palate Mutation Database |
IRF6 |
44 unique |
| http://bipmed.iqm.unicamp.br/tuberous-sclerosis/ |
LOVD 3.0-17 |
2 genes |
45 variants |
| BIPMed - Variants in tuberous sclerosis patients from Brazil |
TSC1,TSC2 |
44 unique |
| http://genome.igib.res.in/PGx/ |
LOVD 2.0-20 |
43 genes |
35 variants |
| Pharmacogenomics of Infectious Diseases (PGx_IfD ) |
ABCB1,ABCC2,ADAR,APOC3,APOE,BCL2,CD209,CD46,CYP2B6,CYP2C1... |
33 unique |
| https://grenada.lumc.nl/LOVD2/TCS/ |
LOVD 2.0-37 |
2 genes |
26 variants |
| Treacher Collins syndrome variant database |
POLR1C,POLR1D |
22 unique |
| http://genome.igib.res.in/snolovd/ |
LOVD 2.0-35 |
124 genes |
1 variants |
| snoLOVD |
SNORA11B,SNORA12,SNORA13,SNORA16B,SNORA17,SNORA18,SNORA19... |
181 unique |
| http://l3.d-lohmann.de/ |
LOVD 3.0-18 |
1 gene |
0 variants |
| Essen-Eye-Cancer-Genetics |
RB1 |
0 unique |
| http://grenada.lumc.nl/LOVD2/WS/ |
LOVD 2.0-37 |
0 genes |
0 variants |
| LOVD - Leiden Open Variation Database |
|
0 unique |
| http://grenada.lumc.nl/LOVD2/TPI/ |
LOVD 2.0-37 |
0 genes |
0 variants |
| Parkinson's disease Mutation Database |
|
0 unique |
| https://fogellab.neurology.ucla.edu/lovd/ |
LOVD 3.0-21 |
0 genes |
0 variants |
| LOVD - Leiden Open Variation Database |
|
0 unique |
| https://grenada.lumc.nl/LOVD2/PAX2/ |
LOVD 2.0-37 |
0 genes |
0 variants |
| PAX2 variant database |
|
0 unique |
| http://grenada.lumc.nl/LOVD2/mendelian_genes/ |
LOVD 2.0-37 |
0 genes |
0 variants |
| Mendelian genes |
|
0 unique |
| https://grenada.lumc.nl/LOVD2/MD/ |
LOVD 2.0-37 |
0 genes |
0 variants |
| Menkes Disease |
|
0 unique |
| http://bipmed.iqm.unicamp.br/lupus/ |
LOVD 3.0-21 |
0 genes |
0 variants |
| BIPMed Lupus - HG38 |
|
0 unique |
| https://grenada.lumc.nl/LOVD2/uni-hd/5-HT/ |
LOVD 2.0-37 |
0 genes |
0 variants |
| University of Heidelberg Serotonin receptor variant database |
|
0 unique |
(This list is updated daily and shows LOVD 2.0 and 3.0 installations active for the last three months that have the "include in the global LOVD listing" setting enabled. Please allow one day for changes to take effect.)
| Last modified 2020/09/28 10:57:10 CEST |
When using or discussing LOVD please refer to:
Fokkema IF, Taschner PE, Schaafsma GC, Celli J, Laros JF, den Dunnen JT (2011). LOVD v.2.0: the next generation in gene variant databases.
Hum Mutat. 2011 May;32(5):557-63.
|
|
