"GeneDx"[submitter] AND "LOC130060979"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58696	GRCh38/hg38 17q12-21.31(chr17:39199873-45629579)x3	LOC130060786, LOC130060787 +633 more	Copy number gain	See cases	GPathogenic
Select item 59586	GRCh38/hg38 17q21.31(chr17:43570878-44762377)x1	ADAM11, ASB16 +104 more	Copy number loss	See cases	GPathogenic
Select item 1706838	NM_002087.4(GRN):c.-8+236G>A	GRN, LOC130060979	Single nucleotide variant (intron variant)	not provided	GLikely benign

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