"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 3063243	GRCh37/hg19 12q21.1-21.33(chr12:74887087-90469800)x1	ACSS3, ALX1 +43 more	Copy number loss	not specified	GPathogenic
Select item 1527723	GRCh37/hg19 12q21.33(chr12:89841833-89873796)	POC1B	Copy number loss	not specified	GUncertain significance
Select item 1527722	GRCh37/hg19 12q21.33(chr12:89840879-89873796)	POC1B	Copy number loss	not specified	GUncertain significance
Select item 1527721	GRCh37/hg19 12q21.33(chr12:89546727-89911511)	DUSP6, POC1B	Copy number loss	not specified	GUncertain significance

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