"GeneDx"[submitter] AND "CCZ1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59675	GRCh38/hg38 7p22.3-22.1(chr7:45130-6270185)x3	BRAT1, ACTB +381 more	Copy number gain	See cases	GPathogenic
Select item 152010	GRCh38/hg38 7p22.1(chr7:5905831-5981100)x3	CCZ1, LOC106783574 +2 more	Copy number gain	See cases	GLikely benign
Select item 151080	GRCh38/hg38 7p22.1(chr7:5905831-5925893)x3	CCZ1, LOC106783574	Copy number gain	See cases	GUncertain significance
Select item 151061	GRCh38/hg38 7p22.1(chr7:5905831-6014161)x3	AIMP2, CCZ1 +5 more	Copy number gain	See cases	GUncertain significance

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