Related gene-specific medical variations for Gene (Select 4325) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809487	GRCh37/hg19 8q21.3(chr8:89215136-89342944)x1	MMP16	Copy number loss	not provided	GUncertain significance
Select item 979841	GRCh37/hg19 8q21.3(chr8:89055371-89170064)x1	MMP16	Copy number loss	not provided	GUncertain significance
Select item 684884	GRCh37/hg19 8q21.3(chr8:88989315-89115278)x3	MMP16	Copy number gain	not provided	GUncertain significance
Select item 524185	t(5;8)(q13;q11.2)dn	MMP16	Translocation	not specified	GUncertain significance

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