"GeneDx"[submitter] AND "MYH15"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 145994	GRCh38/hg38 3q11.1-13.31(chr3:93819623-116887056)x1	ABHD10, ABI3BP +431 more	Copy number loss	See cases	GPathogenic
Select item 57803	GRCh38/hg38 3q11.1-21.1(chr3:93886671-123216683)x1	TRAT1, TRMT10C +638 more	Copy number loss	See cases	GPathogenic
Select item 57980	GRCh38/hg38 3q13.11-13.31(chr3:104621220-116093884)x3	LOC132088858, LOC132088860 +248 more	Copy number gain	See cases	GPathogenic
Select item 57804	GRCh38/hg38 3q13.13-13.31(chr3:108242572-116169331)x1	ABHD10, ATG3 +186 more	Copy number loss	See cases	GPathogenic
Select item 1275125	NC_000003.12:g.108518915A>G	MYH15	Single nucleotide variant	not provided	GBenign
Select item 1243434	NC_000003.12:g.108519798G>T	MYH15	Single nucleotide variant	not provided	GBenign
Select item 1283838	NC_000003.12:g.108529575T>A	MYH15	Single nucleotide variant	not provided	GBenign

ClinVar