"GeneDx"[submitter] AND "EXOC4"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152912	GRCh38/hg38 7q31.2-36.3(chr7:115459015-159325817)x3	AASS, ABCB8 +1547 more	Copy number gain	See cases	GPathogenic
Select item 152089	GRCh38/hg38 7q33(chr7:133652870-133777167)x1	EXOC4, LOC121175370	Copy number loss	See cases	GLikely benign
Select item 151558	GRCh38/hg38 7q33(chr7:133798485-133889223)x1	EXOC4, LOC101928861	Copy number loss	See cases	GUncertain significance

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