Related gene-specific medical variations for Gene (Select 5212) - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1526430	GRCh37/hg19 2p22.2(chr2:36907777-37013926)	VIT	Copy number loss	not specified	GUncertain significance
Select item 979967	GRCh37/hg19 2p22.2(chr2:36850479-37013926)x1	VIT	Copy number loss	not provided	GUncertain significance
Select item 562498	GRCh37/hg19 2p22.2(chr2:36957586-37029623)x1	VIT	Copy number loss	not provided	GUncertain significance
Select item 92022	NM_053276.4(VIT):c.1031G>T (p.Gly344Val)	VIT (G344V +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

Format

Sort by

Choose Destination

ClinVar