C11orf65[gene] and "single gene"[properties] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2223039	NM_152587.5(C11orf65):c.188A>G (p.Asp63Gly)	C11orf65 (D32G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2254915	NM_152587.5(C11orf65):c.115A>T (p.Ile39Phe)	C11orf65 (I39F)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2685423	GRCh37/hg19 11q22.3(chr11:108250849-108340593)x1	C11orf65	Copy number loss	not provided	GUncertain significance

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