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

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Search results

Items: 52

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1230521	NM_001742.4(CALCR):c.*18C>T	CALCR	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 17636	NM_001742.4(CALCR):c.1340T>C (p.Leu447Pro)	CALCR (L447P +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1289488	NM_001742.4(CALCR):c.1192-326T>C	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1224047	NM_001742.4(CALCR):c.1191+167C>A	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274232	NM_001742.4(CALCR):c.1150-108_1150-107dup	CALCR	Duplication (intron variant)	not provided	GBenign
Select item 1270922	NM_001742.4(CALCR):c.1150-108_1150-105dup	CALCR	Duplication (intron variant)	not provided	GBenign
Select item 1243938	NM_001742.4(CALCR):c.1150-108dup	CALCR	Duplication (intron variant)	not provided	GBenign
Select item 1243075	NM_001742.4(CALCR):c.1150-216C>T	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1250902	NM_001742.4(CALCR):c.1150-238T>A	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222864	NM_001742.4(CALCR):c.1150-311_1150-310dup	CALCR	Duplication (intron variant)	not provided	GBenign
Select item 1261013	NM_001742.4(CALCR):c.1150-301del	CALCR	Deletion (intron variant)	not provided	GBenign
Select item 1237362	NM_001742.4(CALCR):c.1149+149C>G	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1182593	NM_001742.4(CALCR):c.1149+138A>T	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263502	NM_001742.4(CALCR):c.1149+104TATT[5]	CALCR	Microsatellite (intron variant)	not provided	GBenign
Select item 1228199	NM_001742.4(CALCR):c.1149+125A>T	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1244119	NM_001742.4(CALCR):c.1149+123_1149+124insA	CALCR	Insertion (intron variant)	not provided	GBenign
Select item 1274911	NM_001742.4(CALCR):c.1149+72A>G	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230289	NM_001742.4(CALCR):c.931-189_931-187del	CALCR	Deletion (intron variant)	not provided	GBenign
Select item 1237108	NM_001742.4(CALCR):c.931-271G>T	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228298	NM_001742.4(CALCR):c.930+37del	CALCR	Deletion (intron variant)	not provided	GBenign
Select item 1263835	NM_001742.4(CALCR):c.802+245C>A	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1260270	NM_001742.4(CALCR):c.649-78G>C	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251223	NM_001742.4(CALCR):c.649-303A>C	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275083	NM_001742.4(CALCR):c.648+124C>A	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1285837	NM_001742.4(CALCR):c.648G>A (p.Pro216=)	CALCR	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1226058	NM_001742.4(CALCR):c.522-327A>G	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282904	NM_001742.4(CALCR):c.522-979C>T	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282227	NM_001742.4(CALCR):c.522-1226A>G	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270084	NM_001742.4(CALCR):c.522-1229G>A	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230756	NM_001742.4(CALCR):c.522-1328A>C	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1239861	NM_001742.4(CALCR):c.522-1329G>A	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1246386	NM_001742.4(CALCR):c.522-1355C>T	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1271156	NM_001742.4(CALCR):c.522-1472C>G	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286780	NM_001742.4(CALCR):c.521+53C>T	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286997	NM_001742.4(CALCR):c.430-29GTTT[5]	CALCR	Microsatellite (intron variant)	not provided	GBenign
Select item 1178760	NM_001742.4(CALCR):c.430-29GTTT[6]	CALCR	Microsatellite (intron variant)	not provided	GBenign
Select item 1225918	NM_001742.4(CALCR):c.430-77T>G	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245623	NM_001742.4(CALCR):c.430-120T>C	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245484	NM_001742.4(CALCR):c.429+266C>T	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1260439	NM_001742.4(CALCR):c.429+37T>C	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290007	NM_001742.4(CALCR):c.317-192A>G	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1246613	NM_001742.4(CALCR):c.317-282del	CALCR	Deletion (intron variant)	not provided	GBenign
Select item 1246140	NM_001742.4(CALCR):c.316+326A>G	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222355	NM_001742.4(CALCR):c.206-113T>G	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1272830	NM_001742.4(CALCR):c.205+182C>T	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1180947	NM_001742.4(CALCR):c.52-250GT[4]	CALCR	Microsatellite (intron variant)	not provided	GBenign
Select item 1288551	NM_001742.4(CALCR):c.52-264A>T	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1225256	NM_001742.4(CALCR):c.51+105C>T	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274950	NM_001742.4(CALCR):c.-6T>C	CALCR	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 1228304	NM_001742.4(CALCR):c.-26-78dup	CALCR	Duplication (intron variant)	not provided	GBenign
Select item 1277361	NM_001742.4(CALCR):c.-26-8791A>G	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273724	NM_001742.4(CALCR):c.-26-9245G>T	CALCR	Single nucleotide variant (intron variant)	not provided	GBenign

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Items: 52