6a19fa2bf0a5cc04ccccbaf87fd2838d1dd2b9f9
abenetpa
  Tue Jun 16 11:01:29 2020 -0700
added (ClinGen) to track long names refs #25562

diff --git src/hg/makeDb/trackDb/human/trackDb.clinGen.ra src/hg/makeDb/trackDb/human/trackDb.clinGen.ra
index 4ac248e..661a105 100644
--- src/hg/makeDb/trackDb/human/trackDb.clinGen.ra
+++ src/hg/makeDb/trackDb/human/trackDb.clinGen.ra
@@ -1,26 +1,26 @@
 track clinGenSuper
 shortLabel ClinGen
-longLabel Clinical Genome Resource
+longLabel Clinical Genome Resource (ClinGen)
 group phenDis
 superTrack on
 html clinGen 
 
     track dosageSensitivity
     parent clinGenSuper on
     shortLabel ClinGen Dosage Sensitivity
-    longLabel Clinical Genome Resource Dosage Sensitivity Map 
+    longLabel Clinical Genome Resource (ClinGen) Dosage Sensitivity Map 
     visibility pack
     type bigBed 9 +
     itemRgb on
     compositeTrack on
     html clinGenDosage
 
         track clinGenHaplo
         parent dosageSensitivity
         shortLabel ClinGen Haploinsufficiency
         longLabel ClinGen Dosage Sensitivity Map - Haploinsufficiency
         visibility dense
         type bigBed 9 +
         bigDataUrl /gbdb/$D/bbi/clinGen/clinGenHaplo.bb
         mouseOverField _mouseOver
         filterValues.haploScore 0|No evidence available,1|Little evidence for dosage pathogenicity,2|Some evidence for dosage pathogenicity,3|Sufficient evidence for dosage pathogenicity,30|Gene associated with autosomal recessive phenotype,40|Dosage sensitivity unlikely
@@ -28,31 +28,31 @@
 
         track clinGenTriplo
         parent dosageSensitivity
         shortLabel ClinGen Triplosensitivity
         longLabel ClinGen Dosage Sensitivity Map - Triplosensitivity
         visibility dense
         type bigBed 9 +
         bigDataUrl /gbdb//$D/bbi/clinGen/clinGenTriplo.bb
         mouseOverField _mouseOver
         filterValues.triploScore 0|No evidence available,1|Little evidence for dosage pathogenicity,2|Some evidence for dosage pathogenicity,3|Sufficient evidence for dosage pathogenicity,30|Gene associated with autosomal recessive phenotype,40|Dosage sensitivity unlikely
         filterLabel.triploScore Dosage Sensitivity Score
 
     track clinGenCnv
     parent clinGenSuper off
     shortLabel ClinGen Structural Variants
-    longLabel Clinical Genome Resource Structural Variants
+    longLabel Clinical Genome Resource (ClinGen) Structural Variants
     html clinGenSv
     type bigBed 9 +
     itemRgb on
     visibility dense
     mergeSpannedItems off
     bigDataUrl /gbdb/$D/bbi/clinGen/clinGenCnv.bb
     mouseOverField _mouseOver
     filterLabel.size Variant Size
     filterValues.variantType copy_number_loss|loss,copy_number_gain|gain
     filterLabel.variantType Variant Type
     filterValues.clinicalInterpretation Pathogenic|pathogenic,Benign|benign
     filterLabel.clinicalInterpretation Clinical Significance
     url https://www.ncbi.nlm.nih.gov/dbvar/variants/$$
     urlLabel NCBI DbVar:
     urls pubMed="https://pubmed.ncbi.nlm.nih.gov/$$/?from_single_result=$$&expanded_search_query=$$" clinGenId="https://dosage.clinicalgenome.org/clingen_region.cgi?id=$$&page=print"