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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3063340	GRCh37/hg19 14q23.3(chr14:66757630-67086056)x3	GPHN	Copy number gain	not specified	GUncertain significance
Select item 3063326	GRCh37/hg19 14q23.3-24.1(chr14:67491176-68153682)x3	ARG2, ATP6V1D +10 more	Copy number gain	not specified	GUncertain significance
Select item 3063323	GRCh37/hg19 14q23.3(chr14:66924497-67016405)x1	GPHN	Copy number loss	not specified	GUncertain significance
Select item 3063316	GRCh37/hg19 14q23.3(chr14:67148938-67277444)x1	GPHN	Copy number loss	not specified	GUncertain significance
Select item 3063312	GRCh37/hg19 14q23.3(chr14:67361946-67581109)x1	GPHN	Copy number loss	not specified	GPathogenic
Select item 1527823	GRCh37/hg19 14q23.3-24.1(chr14:67443801-68153682)	ARG2, ATP6V1D +10 more	Copy number gain	not specified	GUncertain significance
Select item 1527822	GRCh37/hg19 14q23.3(chr14:67248476-67362863)	GPHN	Copy number loss	not specified	GUncertain significance
Select item 1527821	GRCh37/hg19 14q23.3(chr14:67137765-67315163)	GPHN	Copy number loss	not specified	GUncertain significance

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