"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 3062659	GRCh37/hg19 2p13.3-12(chr2:71076472-76368354)x1	ACTG2, ALMS1 +60 more	Copy number loss	not specified	GLikely pathogenic
Select item 3062614	GRCh37/hg19 2p13.2(chr2:72547570-72763221)x1	EXOC6B	Copy number loss	not specified	GUncertain significance
Select item 3062613	GRCh37/hg19 2p13.2(chr2:72908697-72979393)x1	EXOC6B	Copy number loss	not specified	GUncertain significance
Select item 1526807	GRCh37/hg19 2p13.2(chr2:72598365-72720918)	EXOC6B	Copy number loss	not specified	GUncertain significance

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