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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 776832	NM_032135.4(FSCB):c.2032_2067del (p.Ala678_Glu689del)	FSCB	Deletion (inframe_deletion)	not provided	GLikely benign
Select item 768650	NM_032135.4(FSCB):c.2036_2037insCTCTGAAGTTCAGCCTCCACCAGCTGAGGAGGCCCC (p.Pro679_Ala680insSerGluValGlnProProProAlaGluGluAlaPro)	FSCB	Microsatellite (inframe_insertion)	not provided	GBenign
Select item 715665	NM_032135.4(FSCB):c.1533A>G (p.Pro511=)	FSCB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 781129	NM_032135.4(FSCB):c.420G>A (p.Trp140Ter)	FSCB (W140*)	Single nucleotide variant (nonsense)	not provided	GLikely benign
Select item 709937	NM_032135.4(FSCB):c.355C>T (p.Pro119Ser)	FSCB (P119S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 773041	NM_032135.4(FSCB):c.273C>T (p.Thr91=)	FSCB	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2426634	NC_000014.8:g.(?_44820816)_(45645917_?)del	C14orf28, FANCM +5 more	Deletion	Fanconi anemia	GPathogenic

ClinVar