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
KIAA1217	gene	KIAA1217	Expert Review Amber;Literature	VACTERL-like phenotypes	Limb disorders	Dysmorphic and congenital abnormality syndromes	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	vertebral malformations				32369272		False	2	0;100;0	1.35	False		ENSG00000120549	ENSG00000120549	HGNC:25428													
MIR17HG	gene	MIR17HG	Expert Review Amber;Literature	VACTERL-like phenotypes	Limb disorders	Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Feingold syndrome;Feingold syndrome 2, 614326;FS2;Brachydactyly with short stature and microcephaly				21892160;19344873;25391829;26360630		False	2	50;50;0	1.35	True		ENSG00000215417	ENSG00000215417	HGNC:23564