Entity Name	Entity type	Gene Symbol	Sources(; separated)	Level4	Level3	Level2	Model_Of_Inheritance	Phenotypes	Omim	Orphanet	HPO	Publications	Description	Flagged	GEL_Status	UserRatings_Green_amber_red	version	ready	Mode of pathogenicity	EnsemblId(GRch37)	EnsemblId(GRch38)	HGNC	Position Chromosome	Position GRCh37 Start	Position GRCh37 End	Position GRCh38 Start	Position GRCh38 End	STR Repeated Sequence	STR Normal Repeats	STR Pathogenic Repeats	Region Haploinsufficiency Score	Region Triplosensitivity Score	Region Required Overlap Percentage	Region Variant Type	Region Verbose Name
ERCC6	gene	ERCC6	Eligibility statement prior genetic testing;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;Other;Radboud University Medical Center, Nijmegen;UKGTN	Cockayne syndrome	DNA repair disorders	Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Cockayne syndrome, type B;Cockayne syndrome phenotype and UV-sensitive syndrome;PMID: 26204423				26204423;26749132		False	3	100;0;0	0.30	True	Other - please provide details in the comments	ENSG00000225830	ENSG00000225830	HGNC:3438													
ERCC8	gene	ERCC8	Eligibility statement prior genetic testing;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;Other;Radboud University Medical Center, Nijmegen;UKGTN	Cockayne syndrome	DNA repair disorders	Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Cockayne syndrome, type A;Cockayne syndrome phenotype and UV-sensitive syndrome;PMID: 26204423				26204423		False	3	100;0;0	0.30	True	Other - please provide details in the comments	ENSG00000049167	ENSG00000049167	HGNC:3439