"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "BCL9"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 718807	NM_004326.4(BCL9):c.661-8G>T	BCL9	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 708511	NM_004326.4(BCL9):c.905G>A (p.Gly302Asp)	BCL9 (G302D)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 752986	NM_004326.4(BCL9):c.1147G>A (p.Ala383Thr)	BCL9 (A383T)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 777923	NM_004326.4(BCL9):c.1455G>A (p.Arg485=)	BCL9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 745937	NM_004326.4(BCL9):c.2298A>G (p.Pro766=)	BCL9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2425333	NC_000001.10:g.(?_146714354)_(147381384_?)del	ACP6, BCL9 +3 more	Deletion	Cataract 1 multiple types	GPathogenic
Select item 1440405	NC_000001.10:g.(?_146714354)_(147381384_?)dup	ACP6, BCL9 +3 more	Duplication	Cataract 1 multiple types	GUncertain significance
Select item 1003645	NC_000001.10:g.(?_130980840)_(248900000_?)dup	ARL8A, CNIH4 +956 more	Duplication	Gastrointestinal stromal tumor +2 more	GUncertain significance

ClinVar