"GeneDx"[submitter] AND "LOC126860875"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57885	GRCh38/hg38 10p12.31(chr10:20776151-21435636)x3	C10orf113, LINC02643 +12 more	Copy number gain	See cases	GUncertain significance
Select item 1237015	NM_006393.3(NEBL):c.2148+280A>G	LOC126860875, NEBL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 676594	NM_006393.3(NEBL):c.2148+209A>G	LOC126860875, NEBL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 164744	NM_006393.3(NEBL):c.2148+4T>C	LOC126860875, NEBL	Single nucleotide variant (intron variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 201909	NM_006393.3(NEBL):c.2101C>A (p.Pro701Thr)	LOC126860875, NEBL (P701T)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GUncertain significance
Select item 45491	NM_006393.3(NEBL):c.2080C>T (p.Arg694Trp)	LOC126860875, NEBL (R694W)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 45490	NM_006393.3(NEBL):c.2057T>C (p.Val686Ala)	LOC126860875, NEBL (V686A)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GBenign/Likely benign

ClinVar