"GeneDx"[submitter] AND "NTRK3"[gene] - ClinVar

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Items: 40

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58580	GRCh38/hg38 15q25.2-26.3(chr15:84169153-101904929)x3	ABHD2, ACAN +611 more	Copy number gain	See cases	GPathogenic
Select item 1285761	NM_001012338.3(NTRK3):c.*197AT[12]	NTRK3	Microsatellite (3 prime UTR variant)	not provided	GBenign
Select item 1226773	NM_001012338.3(NTRK3):c.*99G>A	NTRK3	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1236984	NM_001012338.3(NTRK3):c.2334+164del	NTRK3	Deletion (intron variant)	not provided	GBenign
Select item 1249082	NM_001012338.3(NTRK3):c.2334+38G>A	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275729	NM_001012338.3(NTRK3):c.2175+223G>T	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1223297	NM_001012338.3(NTRK3):c.2134-110T>C	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1260811	NM_001012338.3(NTRK3):c.2134-175T>C	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1284241	NM_001012338.3(NTRK3):c.2133+252T>C	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276265	NM_001012338.3(NTRK3):c.1889+77T>G	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275495	NM_001012338.3(NTRK3):c.1717-271G>A	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238859	NM_001012338.3(NTRK3):c.1716+260T>C	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229466	NM_001012338.3(NTRK3):c.1586-39049C>A	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251663	NM_001012338.3(NTRK3):c.1586-39051G>A	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1295982	NM_001012338.3(NTRK3):c.1586-40804T>C	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1295997	NM_001012338.3(NTRK3):c.1585+202G>A	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251369	NM_001012338.3(NTRK3):c.1488C>G (p.Ala496=)	NTRK3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1178216	NM_001012338.3(NTRK3):c.1396+339A>G	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274861	NM_001012338.3(NTRK3):c.1396+310C>T	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277211	NM_001012338.3(NTRK3):c.1396+120C>G	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1295969	NM_001012338.3(NTRK3):c.1293+280A>T	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1272721	NM_001012338.3(NTRK3):c.1229-273G>C	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1239549	NM_001012338.3(NTRK3):c.1229-301A>C	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221352	NM_001012338.3(NTRK3):c.908-52A>G	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1181452	NM_001012338.3(NTRK3):c.623-260C>T	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1227513	NM_001012338.3(NTRK3):c.573C>T (p.Asn191=)	NTRK3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1286942	NM_001012338.3(NTRK3):c.465-151C>A	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1254943	NM_001012338.3(NTRK3):c.465-195A>T	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286442	NM_001012338.3(NTRK3):c.396-150AAG[17]	NTRK3	Microsatellite (intron variant)	not provided	GBenign
Select item 1295963	NM_001012338.3(NTRK3):c.396-150AAG[9]	NTRK3	Microsatellite (intron variant)	not provided	GBenign
Select item 1273002	NM_001012338.3(NTRK3):c.396-150AAG[14]	NTRK3	Microsatellite (intron variant)	not provided	GBenign
Select item 1263548	NM_001012338.3(NTRK3):c.396-150AAG[13]	NTRK3	Microsatellite (intron variant)	not provided	GBenign
Select item 1261293	NM_001012338.3(NTRK3):c.396-150AAG[15]	NTRK3	Microsatellite (intron variant)	not provided	GBenign
Select item 1249153	NM_001012338.3(NTRK3):c.395+244C>T	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1250468	NM_001012338.3(NTRK3):c.395+63C>T	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282760	NM_001012338.3(NTRK3):c.323+120G>C	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228998	NM_001012338.3(NTRK3):c.249-221T>A	NTRK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264869	NM_001012338.3(NTRK3):c.248+320dup	NTRK3, NTRK3-AS1	Duplication (intron variant)	not provided	GBenign
Select item 1234989	NM_001012338.3(NTRK3):c.248+325T>A	NTRK3, NTRK3-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 253516	GRCh37/hg19 15q22.31-26.3(chr15:64637227-102509910)x3	AAGAB, ABHD17C +278 more	Copy number gain	See cases	GPathogenic

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Items: 40