Related gene-specific medical variations for Gene (Select 9194) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1808515	GRCh37/hg19 12q14.1(chr12:59615966-61926383)x1	SLC16A7	Copy number loss	not provided	GUncertain significance
Select item 815530	GRCh37/hg19 12q14.1(chr12:59659908-60004443)x3	SLC16A7	Copy number gain	not provided	GUncertain significance
Select item 563944	GRCh37/hg19 12q14.1(chr12:60173814-60610476)x3	SLC16A7	Copy number gain	not provided	GUncertain significance
Select item 563922	GRCh37/hg19 12q14.1(chr12:60161907-60415132)x1	SLC16A7	Copy number loss	not provided	GLikely benign

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