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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3063432	GRCh37/hg19 1p31.1(chr1:72399667-72433308)x1	NEGR1	Copy number loss	not specified	GUncertain significance
Select item 3062744	GRCh37/hg19 1p31.1(chr1:72126327-73436923)x3	NEGR1, NEGR1-IT1	Copy number gain	not specified	GUncertain significance
Select item 1527071	GRCh37/hg19 1p31.1(chr1:71714401-72002854)	NEGR1	Copy number loss	not specified	GUncertain significance
Select item 1527060	GRCh37/hg19 1p31.3-22.1(chr1:68180293-92731957)	MCOLN3, MIGA1 +97 more	Copy number loss	not specified	GPathogenic

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