Related gene-specific medical variations for Gene (Select 84898) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685370	GRCh37/hg19 10p12.31(chr10:19937554-20399617)x1	PLXDC2	Copy number loss	not provided	GUncertain significance
Select item 1809427	GRCh37/hg19 10p12.31(chr10:19973105-20725104)x3	PLXDC2	Copy number gain	not provided	GUncertain significance
Select item 1808821	GRCh37/hg19 10p12.31(chr10:20247074-20306881)x1	PLXDC2	Copy number loss	not provided	GUncertain significance
Select item 1808530	GRCh37/hg19 10p12.31(chr10:19516264-20934189)x1	PLXDC2	Copy number loss	not provided	GUncertain significance
Select item 1807964	GRCh37/hg19 10p12.31(chr10:20391795-20481555)x1	PLXDC2	Copy number loss	not provided	GUncertain significance
Select item 980366	GRCh37/hg19 10p12.31(chr10:19814841-20477255)x1	PLXDC2	Copy number loss	not provided	GUncertain significance
Select item 815324	GRCh37/hg19 10p12.31(chr10:19175479-20260050)x3	PLXDC2	Copy number gain	not provided	GUncertain significance

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