"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "XKRX"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2661046	NM_212559.3(XKRX):c.1107C>T (p.Phe369=)	XKRX	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2661047	NM_212559.3(XKRX):c.765C>G (p.Leu255=)	XKRX	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2661048	NM_212559.3(XKRX):c.288A>G (p.Lys96=)	LOC126863293, XKRX	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3024654	GRCh37/hg19 Xq12-28(chrX:67292994-155240074)x3	ALG13, AMMECR1 +488 more	Copy number gain	not provided	GPathogenic
Select item 493606	GRCh37/hg19 Xq22.1(chrX:99742359-100759773)x3	CENPI, CSTF2 +18 more	Copy number gain	not provided	GLikely pathogenic
Select item 425520	GRCh37/hg19 Xp22.2-q25(chrX:11692290-121187337)x2	AWAT2, BCLAF3 +568 more	Copy number gain	not provided	GUncertain significance

ClinVar