"GeneDx"[submitter] AND "NDUFB8"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58777	GRCh38/hg38 10q23.33-24.32(chr10:93181201-101356779)x1	LOC130004555, LOC130004556 +375 more	Copy number loss	See cases	GPathogenic
Select item 1268122	NM_005004.4(NDUFB8):c.212+59G>T	NDUFB8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264789	NM_005004.4(NDUFB8):c.85+36G>A	NDUFB8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1244849	NC_000010.11:g.100529986C>G	NDUFB8	Single nucleotide variant	not provided	GBenign

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