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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3062919	GRCh37/hg19 6p25.1(chr6:5200686-5396374)x1	FARS2, LYRM4	Copy number loss	not specified	GUncertain significance
Select item 3062905	GRCh37/hg19 6p25.1(chr6:5216289-5316709)x1	FARS2, LYRM4	Copy number loss	not specified	GUncertain significance
Select item 3062881	GRCh37/hg19 6p25.1(chr6:5172636-5200031)x1	LYRM4	Copy number loss	not specified	GPathogenic
Select item 1527219	GRCh37/hg19 6p25.1(chr6:5248338-5395099)	FARS2, LYRM4	Copy number loss	not specified	GUncertain significance
Select item 1527218	GRCh37/hg19 6p25.1(chr6:5210792-5339437)	LYRM4, FARS2	Copy number loss	not specified	GUncertain significance
Select item 1527217	GRCh37/hg19 6p25.1(chr6:5081988-5401617)	FARS2, LYRM4 +1 more	Copy number gain	not specified	GUncertain significance

ClinVar