Related gene-specific medical variations for Gene (Select 92906) - ClinVar

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

Format

Sort by

Choose Destination

Links from Gene

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 687611	GRCh37/hg19 2p22.1(chr2:38791220-38861082)x3	HNRNPLL	Copy number gain	not provided	GUncertain significance
Select item 686954	GRCh37/hg19 2p22.1(chr2:38791220-38861082)x3	HNRNPLL	Copy number gain	not provided	GUncertain significance
Select item 686481	GRCh37/hg19 2p22.1(chr2:38791220-38861082)x3	HNRNPLL	Copy number gain	not provided	GUncertain significance
Select item 686358	GRCh37/hg19 2p22.1(chr2:38791220-38861082)x3	HNRNPLL	Copy number gain	not provided	GUncertain significance

Format

Sort by

Choose Destination