"ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laborato - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3062585	GRCh37/hg19 Xp22.2(chrX:11962592-12214448)	FRMPD4	Copy number gain	not specified	GUncertain significance
Select item 3062573	GRCh37/hg19 Xp22.2(chrX:12690537-12751085)	FRMPD4	Copy number gain	not specified	GUncertain significance
Select item 3062567	GRCh37/hg19 Xp22.2(chrX:11688762-12188817)	FRMPD4, MSL3	Copy number gain	not specified	GUncertain significance
Select item 3062511	GRCh37/hg19 Xp22.33-11.1(chrX:168546-58364114)	ACE2, ACOT9 +314 more	Copy number loss	not specified	GPathogenic
Select item 3062472	GRCh37/hg19 Xp22.2(chrX:12166195-12694914)	FRMPD4	Copy number gain	not specified	GUncertain significance
Select item 3062471	GRCh37/hg19 Xp22.33-11.21(chrX:168546-55653170)	ACE2, ACOT9 +305 more	Copy number loss	not specified	GPathogenic

ClinVar