Related gene-specific medical variations for Gene (Select 23543) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1340218	GRCh37/hg19 22q12.3(chr22:36319058-36403971)x1	RBFOX2	Copy number loss	not provided	GUncertain significance
Select item 689048	GRCh37/hg19 22q12.3(chr22:36202468-36292702)x1	RBFOX2	Copy number loss	not provided	GUncertain significance
Select item 688614	GRCh37/hg19 22q12.3(chr22:36390903-36480099)x3	RBFOX2	Copy number gain	not provided	GUncertain significance
Select item 687461	GRCh37/hg19 22q12.3(chr22:36395153-36480099)x3	RBFOX2	Copy number gain	not provided	GUncertain significance
Select item 686248	GRCh37/hg19 22q12.3(chr22:36395153-36480099)x3	RBFOX2	Copy number gain	not provided	GUncertain significance
Select item 152135	GRCh38/hg38 22q12.3(chr22:35893428-35931051)x1	RBFOX2	Copy number loss	See cases	GUncertain significance

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