"GeneDx"[submitter] AND "TMTC2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59816	GRCh38/hg38 12q21.2-21.31(chr12:77564757-85370822)x3	ACSS3, ALX1 +66 more	Copy number gain	See cases	GPathogenic
Select item 151285	GRCh38/hg38 12q21.31(chr12:82697865-82746258)x1	TMTC2	Copy number loss	See cases	GBenign
Select item 152630	GRCh38/hg38 12q21.31(chr12:82970882-82994642)x4	TMTC2	Copy number gain	See cases	GLikely benign

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