"GeneDx"[submitter] AND "EHBP1L1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152827	GRCh38/hg38 11q13.1(chr11:65327786-65626431)x3	DPF2, EHBP1L1 +80 more	Copy number gain	See cases	GUncertain significance
Select item 152640	GRCh38/hg38 11q13.1(chr11:65520831-65695349)x3	EHBP1L1, FAM89B +45 more	Copy number gain	See cases	GUncertain significance
Select item 1265858	NM_001099409.3(EHBP1L1):c.1613T>G (p.Val538Gly)	EHBP1L1 (V538G)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign

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