"GeneDx"[submitter] AND "LOC130004821"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59728	GRCh38/hg38 10q26.11-26.3(chr10:117866565-133554210)x3	ABRAXAS2, ACADSB +514 more	Copy number gain	See cases	GPathogenic
Select item 57911	GRCh38/hg38 10q26.11(chr10:118832386-119400019)x3	DENND10, EIF3A +36 more	Copy number gain	See cases	GUncertain significance
Select item 768395	NM_199461.4(NANOS1):c.235T>A (p.Ser79Thr)	LOC130004821, NANOS1 (S79T)	Single nucleotide variant (missense variant)	not provided	GBenign

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