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

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1215621	NM_001007792.1(NTRK1):c.10-67C>G	INSRR, NTRK1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1310344	NM_001007792.1(NTRK1):c.72C>G (p.Thr24=)	INSRR, NTRK1 (M1122I)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1187999	NM_001007792.1(NTRK1):c.122+160G>C	INSRR, NTRK1	Single nucleotide variant (intron variant)	not provided	GLikely benign

Format

Sort by

Choose Destination