"GeneDx"[submitter] AND "LINC01779"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58210	GRCh38/hg38 12q12(chr12:39651727-41240339)x3	CNTN1, LINC01779 +25 more	Copy number gain	See cases	GUncertain significance
Select item 1297877	NC_000012.12:g.40224884T>C	LINC01779, LOC130007688 +1 more	Single nucleotide variant	not provided	GBenign
Select item 1196141	NC_000012.12:g.40224903G>A	LINC01779, LOC130007688 +1 more	Single nucleotide variant (genic upstream transcript variant)	not provided	GLikely benign

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