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

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59657	GRCh38/hg38 10p15.3-12.31(chr10:69261-19184047)x3	LOC126860819, LOC126860820 +680 more	Copy number gain	See cases	GPathogenic
Select item 1316887	NM_003380.5(VIM):c.-147-284C>T	VIM, VIM-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1246121	NM_003380.5(VIM):c.-147-165G>C	VIM, VIM-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316913	NM_003380.5(VIM):c.-147-69G>C	VIM, VIM-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1277994	NM_003380.5(VIM):c.-27C>T	VIM, VIM-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1277763	NM_003380.5(VIM):c.-22G>C	VIM, VIM-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Cataract 30 +1 more	GBenign
Select item 1289151	NM_003380.5(VIM):c.563+122C>G	LOC130003453, VIM	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1262889	NM_003380.5(VIM):c.564-274dup	VIM	Duplication (intron variant)	not provided	GBenign
Select item 1229776	NM_003380.5(VIM):c.564-139C>T	VIM	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317705	NM_003380.5(VIM):c.564-27C>A	VIM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1243925	NM_003380.5(VIM):c.624+210dup	VIM	Duplication (intron variant)	not provided	GBenign
Select item 1239740	NM_003380.5(VIM):c.624+210del	VIM	Deletion (intron variant)	not provided	GBenign
Select item 1318442	NM_003380.5(VIM):c.625-136C>T	VIM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1316436	NM_003380.5(VIM):c.720+18C>T	VIM	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 474044	NM_003380.5(VIM):c.813C>T (p.Asp271=)	VIM	Single nucleotide variant (synonymous variant)	Cataract 30 +1 more	GBenign
Select item 702034	NM_003380.5(VIM):c.879C>G (p.Ser293=)	VIM	Single nucleotide variant (synonymous variant)	Cataract 30 +1 more	GBenign/Likely benign
Select item 1225435	NM_003380.5(VIM):c.882+136C>T	VIM	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277794	NM_003380.5(VIM):c.883-287C>T	VIM	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1225132	NM_003380.5(VIM):c.1008+99G>A	VIM	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316918	NM_003380.5(VIM):c.1009-36A>G	VIM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 474043	NM_003380.5(VIM):c.1009-10C>T	VIM	Single nucleotide variant (intron variant)	Cataract 30 +1 more	GBenign
Select item 1296973	NM_003380.5(VIM):c.1229+89C>G	VIM	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1267573	NM_003380.5(VIM):c.1229+115G>A	VIM	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317285	NM_003380.5(VIM):c.1230-208T>C	VIM	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1235195	NM_003380.5(VIM):c.1274-122C>G	VIM	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1259940	NM_003380.5(VIM):c.1360-200G>A	VIM	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317794	NM_003380.5(VIM):c.*55C>T	VIM	Single nucleotide variant (3 prime UTR variant)	not provided	GLikely benign
Select item 1288184	NM_003380.5(VIM):c.*247C>T	VIM	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1283433	NM_003380.5(VIM):c.*292G>T	VIM	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign

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Items: 29