"GeneDx"[submitter] AND "SMYD3"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58116	GRCh38/hg38 1q32.2-44(chr1:209646207-248931113)x3	LOC120908923, LOC120947224 +1352 more	Copy number gain	See cases	GPathogenic
Select item 59654	GRCh38/hg38 1q43-44(chr1:242828731-248891309)x3	TFB2M, TRE-CTC2-1 +238 more	Copy number gain	See cases	GPathogenic
Select item 151310	GRCh38/hg38 1q44(chr1:246202303-246759911)x3	CNST, LINC01743 +22 more	Copy number gain	See cases	GLikely benign
Select item 152671	GRCh38/hg38 1q44(chr1:246338331-246415872)x1	LOC129388803, SMYD3	Copy number loss	See cases	GBenign
Select item 145943	GRCh38/hg38 1q44(chr1:246386899-246415872)x1	SMYD3	Copy number loss	See cases	GLikely benign
Select item 253636	GRCh37/hg19 1q42.2-44(chr1:234050864-249213059)x3	ACTN2, ADSS2 +105 more	Copy number gain	See cases	GPathogenic
Select item 253578	GRCh37/hg19 1q43-44(chr1:242357208-246378823)x1	ADSS2, AKT3 +12 more	Copy number loss	See cases	GPathogenic
Select item 253547	GRCh37/hg19 1q43-44(chr1:243103401-249119318)x1	OR2L2, OR2L8 +66 more	Copy number loss	See cases	GPathogenic

ClinVar