ClinVar for Gene (Select 28908) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 148476	GRCh38/hg38 2p11.2(chr2:87375475-90282666)x3	CYTOR, EIF2AK3 +101 more	Copy number gain	See cases	GUncertain significance
Select item 146363	GRCh38/hg38 2p11.2-11.1(chr2:87098178-91884275)x3	CYTOR, EIF2AK3 +104 more	Copy number gain	See cases	GUncertain significance
Select item 145759	GRCh38/hg38 2p11.2(chr2:88838079-89030495)x0	IGK, IGKC +14 more	Copy number loss	See cases	GBenign
Select item 145403	GRCh38/hg38 2p12-11.2(chr2:77025216-90282666)x3	ATOH8, C2orf68 +302 more	Copy number gain	See cases	GPathogenic

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