Query all public LOVD installations

Query all public LOVD instances:
Examples: Precise: chr15:g.40699840C>T, Range: chr13:32936732-32936735.
Instead of "chr15", you can also use a reference sequence, e.g., NC_000015.9:g.40699840C>T. The given build will then be derived from your input.

LOVDs currently support only one genome build; if no results are found, you may want to repeat your query using a different genome build.
LOVD contains for hg18 ~2K unique variants, hg19 ~3.0M unique variants, and hg38 ~1.4M.
This service queries the variant's location, i.e. results of other variants on the same location will show as well. When searching using a ranged variant in HGVS format, only variants exactly matching that range will be returned. When searching using a range (2nd example above), all variants within that range will be returned (to a max of 50).

When using or discussing LOVD please refer to:
Fokkema IF, Kroon M, López Hernández JA, Asscheman D, Lugtenburg I, Hoogenboom J, den Dunnen JT. The LOVD3 platform: efficient genome-wide sharing of genetic variants. Eur J Hum Genet (2021). https://doi.org/10.1038/s41431-021-00959-x.

A recommended system of the Human Variome Project LOVD has received funding from the European Community's Seventh Framework Programme
(FP7/2007-2013) under grant agreement nº 200754 - the GEN2PHEN project.
©2004-2024 Leiden University Medical Center, Netherlands
Ivo F.A.C. Fokkema BSc., Prof. Johan T. den Dunnen PhD
A IRDiRC recognized resource