Related gene-specific medical variations for Gene (Select 25771) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685683	GRCh37/hg19 22q13.31(chr22:47419653-47480001)x1	TBC1D22A	Copy number loss	not provided	GUncertain significance
Select item 686283	GRCh37/hg19 22q13.31(chr22:47325026-47432083)x1	TBC1D22A	Copy number loss	not provided	GUncertain significance
Select item 564982	GRCh37/hg19 22q13.31(chr22:47247000-47377175)x1	TBC1D22A	Copy number loss	not provided	GLikely benign
Select item 443785	GRCh37/hg19 22q13.31(chr22:47166175-47567936)x1	TBC1D22A	Copy number loss	See cases	GLikely benign

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