"GeneDx"[submitter] AND "LOC130057159"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57881	GRCh38/hg38 15q21.2-22.2(chr15:50864913-59646577)x1	ADAM10, ALDH1A2 +287 more	Copy number loss	See cases	GPathogenic
Select item 57882	GRCh38/hg38 15q21.3-22.2(chr15:57567950-63019415)x1	ADAM10, ALDH1A2 +163 more	Copy number loss	See cases	GPathogenic
Select item 1233353	NC_000015.10:g.58750164C>A	ADAM10, LOC130057159	Single nucleotide variant	not provided	GBenign
Select item 1276470	NC_000015.10:g.58750253G>A	ADAM10, LOC130057159	Single nucleotide variant	not provided	GBenign

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