"GeneDx"[submitter] AND "MEOX1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58696	GRCh38/hg38 17q12-21.31(chr17:39199873-45629579)x3	LOC130060786, LOC130060787 +633 more	Copy number gain	See cases	GPathogenic
Select item 59586	GRCh38/hg38 17q21.31(chr17:43570878-44762377)x1	ADAM11, ASB16 +104 more	Copy number loss	See cases	GPathogenic
Select item 1236576	NM_004527.4(MEOX1):c.643-220C>T	MEOX1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265705	NM_004527.4(MEOX1):c.470-174A>G	MEOX1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222503	NM_004527.4(MEOX1):c.469+218A>G	MEOX1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 259424	NM_004527.4(MEOX1):c.80C>T (p.Ser27Leu)	MEOX1 (S27L)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GBenign

ClinVar