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.hg19.tab src/hg/htdocs/inc/recTrackSets.hg19.tab
index 0794c4bf6f4..d2272d7f8e2 100644
--- src/hg/htdocs/inc/recTrackSets.hg19.tab
+++ src/hg/htdocs/inc/recTrackSets.hg19.tab
@@ -1,16 +1,17 @@
 # List of curated sessions for clinical, etc. users
 #
 # 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	SNVs%20Clinical	Assess potential disease contributions of single nucleotide variants in coding regions
 Clinical CNVs	View	CNVs%20Clinical	Assess potential disease contributions of structural variants in coding regions
 Non-coding SNVs	View	Non%20coding%20SNVs	Investigate functional aspects of non-coding variants
 Determine Exon Relevance	View	Exon_Relevance_hg19	Examine if variants are present in an exon required for the function of the expressed gene product
 Problematic Regions	View	Problematic%20Regions	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_hg19	Assess potential disease contribution of variants on BRCA1 and BRCA2 according to the ENIGMA VCEP guidelines
+InSiGHT Lynch Syndrome VCEP	View	insightVcepHg19	Assess potential disease contribution of variants on MLH1, MSH2, MSH6, and PMS2 according to the InSiGHT VCEP guidelines