"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "GSX2"[gene - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2654757	NM_133267.3(GSX2):c.34A>G (p.Ile12Val)	GSX2 (I12V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2654758	NM_133267.3(GSX2):c.135G>A (p.Val45=)	GSX2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3024631	GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3	TMA16, CXCL1 +537 more	Copy number gain	not provided	GPathogenic

Format

Sort by

Choose Destination