Related gene-specific medical variations for Gene (Select 4602) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 495140	t(6;9)(q23.3;p22.3)	MYB, NFIB	Translocation	Adenoid cystic carcinoma	GPathogenic
Select item 495139	t(6;9)(q23.3;p22.3)	MYB, NFIB	Translocation	Adenoid cystic carcinoma	GPathogenic
Select item 495138	t(6;9)(q23.3;p22.3)	NFIB, MYB	Translocation	Adenoid cystic carcinoma	GPathogenic
Select item 495137	t(6;9)(q23.3;p22.3)	MYB, NFIB	Translocation	Adenoid cystic carcinoma	GPathogenic

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