Related gene-specific medical variations for Gene (Select 53336) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685755	GRCh37/hg19 Xq21.31(chrX:87847607-88259035)x2	CPXCR1	Copy number gain	not provided	GUncertain significance
Select item 2685753	GRCh37/hg19 Xq21.31(chrX:87838376-88098049)x2	CPXCR1	Copy number gain	not provided	GUncertain significance
Select item 1340950	GRCh37/hg19 Xq21.31(chrX:87837389-88164567)x1	CPXCR1	Copy number loss	not provided	GLikely benign
Select item 979834	GRCh37/hg19 Xq21.31(chrX:87838375-88164567)x0	CPXCR1	Copy number loss	not provided	GUncertain significance
Select item 442802	GRCh37/hg19 Xq21.31(chrX:88009699-88684010)x2	CPXCR1	Copy number gain	See cases	GUncertain significance
Select item 442765	GRCh37/hg19 Xq21.31(chrX:87838375-88164567)x1	CPXCR1	Copy number loss	See cases	GUncertain significance
Select item 442764	GRCh37/hg19 Xq21.31(chrX:87838375-88164567)x0	CPXCR1	Copy number loss	See cases	GUncertain significance
Select item 442089	GRCh37/hg19 Xq21.31(chrX:87837389-88164567)x1	CPXCR1	Copy number loss	See cases	GUncertain significance
Select item 394505	GRCh37/hg19 Xq21.31(chrX:88002288-88348495)x0	CPXCR1	Copy number loss	See cases	GLikely benign

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