"GeneDx"[submitter] AND "ALX1"[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 1226313	NM_006982.3(ALX1):c.226+193C>A	ALX1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229878	NM_006982.3(ALX1):c.532-97dup	ALX1	Duplication (intron variant)	not provided	GBenign

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