159988dc8595c08c87164253d8d09997c925661c
lrnassar
  Tue Apr 14 13:03:07 2026 -0700
Creating a new RTS for the InSiGHT VCEP, refs #36582

diff --git src/hg/htdocs/inc/recTrackSets.hg38.tab src/hg/htdocs/inc/recTrackSets.hg38.tab
index aba854afc97..5c6dcf8b988 100644
--- src/hg/htdocs/inc/recTrackSets.hg38.tab
+++ src/hg/htdocs/inc/recTrackSets.hg38.tab
@@ -2,16 +2,16 @@
 #
 # File is tab-separated.  userName and sessionName are fields in hgcentral.namedSessionDb table
 #       sessionName is cgi-decoded to readable text
 # Note that named sessions support description in settings field, however the description in
 #       this file is used in browser (allows non-owner of session, e.g. QA, to edit)
 #       
 # For details on how to update this file, see the wiki: http://genomewiki.ucsc.edu/genecats/index.php/Recommended_Track_Sets
 #       
 # Format: label, userName, sessionName, description
 Clinical SNVs	View	Clinical_SNVs_hg38	Assess potential disease contributions of single nucleotide variants in coding regions
 Clinical CNVs	View	Clinical_CNVs_hg38	Assess potential disease contributions of structural variants in coding regions
 Non-coding SNVs	View	Non_Coding_SNVs_hg38	Investigate functional aspects of non-coding variants
 Determine Exon Relevance	View	Exon_Relevance_hg38	Examine if variants are present in an exon required for the function of the expressed gene product
 Problematic Regions	View	Problematic_Regions_hg38	Evaluate if annotations are on potential low confidence regions due to high homology or other reported concerns
 ENIGMA BRCA1/BRCA2 VCEP	View	BRCA1_BRCA2_ENIGMA_hg38	Assess potential disease contribution of variants on BRCA1 and BRCA2 according to the ENIGMA VCEP guidelines
-
+InSiGHT Lynch Syndrome VCEP	View	insightVcepHg38	Assess potential disease contribution of variants on MLH1, MSH2, MSH6, and PMS2 according to the InSiGHT VCEP guidelines