"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LY9"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 729550	NM_002348.4(LY9):c.39T>C (p.Pro13=)	LY9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 783299	NM_002348.4(LY9):c.586C>A (p.Pro196Thr)	LY9 (P196T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 639872	NC_000001.10:g.(?_160786670)_(161332233_?)dup	ADAMTS4, APOA2 +63 more	Duplication	Gastrointestinal stromal tumor +1 more	GUncertain significance
Select item 726709	NM_002348.4(LY9):c.1432C>T (p.Arg478Ter)	LY9 (R388* +1 more)	Single nucleotide variant (nonsense)	not provided	GLikely benign
Select item 1411942	NC_000001.10:g.(?_158581054)_(162750036_?)dup	LY9, MNDA +90 more	Duplication	Autoimmune interstitial lung disease-arthritis syndrome	GUncertain significance
Select item 1003645	NC_000001.10:g.(?_130980840)_(248900000_?)dup	ARL8A, CNIH4 +956 more	Duplication	Gastrointestinal stromal tumor +2 more	GUncertain significance
Select item 830661	NC_000001.11:g.(?_160816880)_(161362518_?)dup	ADAMTS4, APOA2 +24 more	Duplication	Gastrointestinal stromal tumor +1 more	GUncertain significance

ClinVar