"GeneDx"[submitter] AND "LOC130006027"[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 1225605	NM_001130144.3(LTBP3):c.3386-50G>A	LOC130006027, LTBP3	Single nucleotide variant (intron variant)	not provided	GBenign

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