"GeneDx"[submitter] AND "LOC126862427"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59517	GRCh38/hg38 16q23.1-24.2(chr16:78704275-87819342)x1	LOC130059506, LOC130059507 +447 more	Copy number loss	See cases	GPathogenic
Select item 59518	GRCh38/hg38 16q23.3-24.1(chr16:81753762-85714791)x1	ADAD2, ATP2C2 +211 more	Copy number loss	See cases	GPathogenic
Select item 1280485	NM_014861.4(ATP2C2):c.2482-19C>G	LOC126862427, ATP2C2 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign

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