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
ADAR	gene	ADAR	Expert Review Red;Victorian Clinical Genetics Services	Chromosome Breakage Disorders		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Dyschromatosis symmetrica hereditaria, MIM# 127400						False	1	0;0;100	1.21	True		ENSG00000160710	ENSG00000160710	HGNC:225													
FANCM	gene	FANCM	Expert Review Red;Victorian Clinical Genetics Services	Chromosome Breakage Disorders		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Fanconi anaemia				28837162		False	1	0;0;100	1.21	True		ENSG00000187790	ENSG00000187790	HGNC:23168													
MAD2L2	gene	MAD2L2	Expert list;Expert Review Red	Chromosome Breakage Disorders		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	"Fanconi anemia, complementation group V, MIM#	617243"				27500492		False	1	0;0;100	1.21	True		ENSG00000116670	ENSG00000116670	HGNC:6764													
MARS	gene	MARS	Expert Review Red;Literature	Chromosome Breakage Disorders		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	"Trichothiodystrophy, MONDO:0018053;Trichothiodystrophy 8, nonphotosensitive, MIM#	619691Trichothiodystrophy 9, nonphotosensitive, MIM#	619692"				33909043		False	1	0;0;100	1.21	True		ENSG00000166986	ENSG00000166986	HGNC:6898