"GeneDx"[submitter] AND "ULK4"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152487	GRCh38/hg38 3p22.1(chr3:41298396-41583960)x1	LOC126806660, ULK4	Copy number loss	See cases	GLikely benign
Select item 57726	GRCh38/hg38 3p22.1(chr3:41880503-42550279)x3	CCK, LOC121009659 +36 more	Copy number gain	See cases	GUncertain significance
Select item 57727	GRCh38/hg38 3p22.1(chr3:41896597-42336619)x3	CCK, LOC121009659 +28 more	Copy number gain	See cases	GUncertain significance
Select item 253640	GRCh37/hg19 3p22.1-21.31(chr3:41104508-44636698)x1	HHATL, ZKSCAN7 +29 more	Copy number loss	See cases	GPathogenic
Select item 253356	GRCh37/hg19 3p22.2-21.31(chr3:37028313-49929220)x3	ABHD5, ACAA1 +177 more	Copy number gain	See cases	GLikely pathogenic

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