"GeneDx"[submitter] AND "LYN"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 60362	GRCh38/hg38 8q12.1(chr8:55423413-58836753)x1	BPNT2, CERNA3 +105 more	Copy number loss	See cases	GPathogenic
Select item 145241	GRCh38/hg38 8q12.1(chr8:55813087-55967049)x3	LOC116186928, LOC124174256 +26 more	Copy number gain	See cases	GBenign
Select item 681455	NM_002350.4(LYN):c.179-3del	LYN	Deletion (intron variant)	not provided	GLikely benign
Select item 253344	GRCh37/hg19 8q12.1(chr8:56405320-57358911)x1	TGS1, PENK +8 more	Copy number loss	See cases	GLikely pathogenic

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