Related gene-specific medical variations for Gene (Select 54986) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685078	GRCh37/hg19 3p22.1(chr3:41683229-41843911)x1	ULK4	Copy number loss	not provided	GUncertain significance
Select item 1808939	GRCh37/hg19 3p22.1(chr3:41589544-41734680)x1	ULK4	Copy number loss	not provided	GUncertain significance
Select item 814437	GRCh37/hg19 3p22.1(chr3:41324847-41635196)x1	ULK4	Copy number loss	not provided	GUncertain significance
Select item 686291	GRCh37/hg19 3p22.1(chr3:41708582-41929706)x1	ULK4	Copy number loss	not provided	GUncertain significance
Select item 545298	NC_000003.12:g.(?_41803875)_(41849829_?)del	ULK4	Deletion	Schizophrenia	GLikely pathogenic
Select item 545297	NC_000003.12:g.(?_41760954)_(41858293_?)del	ULK4	Deletion	Schizophrenia	GLikely pathogenic
Select item 545296	NC_000003.12:g.(?_41609544)_(41811095_?)del	ULK4	Deletion	Schizophrenia	GLikely pathogenic

ClinVar