VCX[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 148107	GRCh38/hg38 Xp22.31(chrX:7573548-7860183)x2	VCX	Copy number gain	See cases	GBenign
Select item 3025302	NM_001393662.1(VCX):c.7C>T (p.Pro3Ser)	VCX (P3S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2659918	NM_001393662.1(VCX):c.216G>A (p.Ala72=)	VCX	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1328292	NM_001393662.1(VCX):c.491T>C (p.Leu164Pro)	VCX (L164P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1206112	NM_001393662.1(VCX):c.548C>T (p.Pro183Leu)	VCX (P183L)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2659919	NM_001393662.1(VCX):c.568G>A (p.Val190Met)	VCX (V190M)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3257662	NM_001393662.1(VCX):c.598A>G (p.Met200Val)	VCX (M200V)	Single nucleotide variant (missense variant)	not provided	GLikely benign

ClinVar