"GeneDx"[submitter] AND "GREM1"[gene] - ClinVar

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Search results

Items: 63

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57876	GRCh38/hg38 15q13.3-14(chr15:32326136-39394068)x1	LOC132090301, LOC132090302 +178 more	Copy number loss	See cases	GPathogenic
Select item 57877	GRCh38/hg38 15q13.3-15.1(chr15:32635803-40233825)x1	ACTC1, AQR +219 more	Copy number loss	See cases	GPathogenic
Select item 1274709	NC_000015.10:g.32717579C>T	GREM1	Single nucleotide variant	not provided	GBenign
Select item 1253919	NC_000015.10:g.32717891G>T	GREM1	Single nucleotide variant	not provided	GBenign
Select item 1297801	NM_013372.7(GREM1):c.-2+50G>A	GREM1, GREM1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1247744	NM_013372.7(GREM1):c.-2+121T>C	GREM1, GREM1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1240993	NM_013372.7(GREM1):c.-2+374G>A	GREM1-AS1, GREM1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1253065	NM_013372.7(GREM1):c.-2+765G>A	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1257647	NM_013372.7(GREM1):c.-2+1279A>G	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238271	NM_013372.7(GREM1):c.-2+1335G>C	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286829	NM_013372.7(GREM1):c.-2+1383del	GREM1	Deletion (intron variant)	not provided	GBenign
Select item 1281851	NM_013372.7(GREM1):c.-2+1489G>T	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294086	NM_013372.7(GREM1):c.-2+1870T>C	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241475	NM_013372.7(GREM1):c.-2+2140A>G	GREM1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1261870	NM_013372.7(GREM1):c.-2+2276G>A	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1179867	NM_013372.7(GREM1):c.-2+2718A>G	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1253385	NM_013372.7(GREM1):c.-2+2857T>A	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222065	NM_013372.7(GREM1):c.-2+3408G>C	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288270	NM_013372.7(GREM1):c.-2+3933C>G	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1256722	NM_013372.7(GREM1):c.-2+4085A>G	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229714	NM_013372.7(GREM1):c.-2+4408T>A	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251562	NM_013372.7(GREM1):c.-2+4844G>A	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263209	NM_013372.7(GREM1):c.-2+5040A>G	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1243347	NM_013372.7(GREM1):c.-2+5098G>C	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1272447	NM_013372.7(GREM1):c.-2+5480del	GREM1	Duplication (intron variant)	not provided	GBenign
Select item 1225581	NM_013372.7(GREM1):c.-2+5479_-2+5480del	GREM1	Deletion (intron variant)	not provided	GBenign
Select item 1278688	NM_013372.7(GREM1):c.-2+5792A>G	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1252719	NM_013372.7(GREM1):c.-2+6116G>C	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234838	NM_013372.7(GREM1):c.-1-6051del	GREM1	Deletion (intron variant)	not provided	GBenign
Select item 1178065	NM_013372.7(GREM1):c.-1-5645del	GREM1	Deletion (intron variant)	not provided	GBenign
Select item 1278032	NM_013372.7(GREM1):c.-1-5343A>G	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1246143	NM_013372.7(GREM1):c.-1-4867G>A	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270936	NM_013372.7(GREM1):c.-1-4827G>A	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1287820	NM_013372.7(GREM1):c.-1-4804A>C	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1224289	NM_013372.7(GREM1):c.-1-4472G>A	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1291111	NM_013372.7(GREM1):c.-1-4004A>C	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1253442	NM_013372.7(GREM1):c.-1-3990C>T	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1292455	NM_013372.7(GREM1):c.-1-3965_-1-3964del	GREM1	Duplication (intron variant)	not provided	GBenign
Select item 1287444	NM_013372.7(GREM1):c.-1-3966_-1-3964del	GREM1	Deletion (intron variant)	not provided	GBenign
Select item 1248799	NM_013372.7(GREM1):c.-1-3967_-1-3964del	GREM1	Deletion (intron variant)	not provided	GBenign
Select item 1280087	NM_013372.7(GREM1):c.-1-3878G>A	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238826	NM_013372.7(GREM1):c.-1-3482_-1-3480del	GREM1	Deletion (intron variant)	not provided	GBenign
Select item 1277057	NM_013372.7(GREM1):c.-1-3347C>T	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1179364	NM_013372.7(GREM1):c.-1-3328T>C	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1291117	NM_013372.7(GREM1):c.-1-3026_-1-3023del	GREM1	Microsatellite (intron variant)	not provided	GBenign
Select item 1247530	NM_013372.7(GREM1):c.-1-2813C>T	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1233198	NM_013372.7(GREM1):c.-1-2624C>T	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263184	NM_013372.7(GREM1):c.-1-2169_-1-2165del	GREM1	Deletion (intron variant)	not provided	GBenign
Select item 1228102	NM_013372.7(GREM1):c.-1-2012T>C	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1223202	NM_013372.7(GREM1):c.-1-1963T>G	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294095	NM_013372.7(GREM1):c.-1-1531C>G	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238220	NM_013372.7(GREM1):c.-1-1501A>G	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1239140	NM_013372.7(GREM1):c.-1-1424C>T	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1281118	NM_013372.7(GREM1):c.-1-1303_-1-1300del	GREM1	Microsatellite (intron variant)	not provided	GBenign
Select item 1268228	NM_013372.7(GREM1):c.-1-980C>G	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1233638	NM_013372.7(GREM1):c.-1-836_-1-835insAA	GREM1	Insertion (intron variant)	not provided	GBenign
Select item 1288795	NM_013372.7(GREM1):c.-1-801G>A	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1272384	NM_013372.7(GREM1):c.-1-683C>T	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234007	NM_013372.7(GREM1):c.-1-309A>T	GREM1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 402911	NM_013372.7(GREM1):c.207C>G (p.Pro69=)	GREM1	Single nucleotide variant (synonymous variant +1 more)	not specified +1 more	GBenign
Select item 1282623	NM_013372.7(GREM1):c.*40C>A	GREM1	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1222045	NM_013372.7(GREM1):c.*224C>T	GREM1	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1278747	NM_013372.7(GREM1):c.*239A>C	GREM1	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign

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Items: 63