"GeneDx"[submitter] AND "CMKLR2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59159	GRCh38/hg38 2q32.2-37.3(chr2:190310736-241892770)x3	LOC129935726, LOC129935727 +1665 more	Copy number gain	See cases	GPathogenic
Select item 152538	GRCh38/hg38 2q33.1-34(chr2:199946494-209985195)x1	ABI2, ADAM23 +293 more	Copy number loss	See cases	GPathogenic
Select item 1238518	NM_001389445.1(CMKLR2):c.919A>G (p.Ile307Val)	CMKLR2 (I307V)	Single nucleotide variant (missense variant)	not provided	GBenign

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