Related gene-specific medical variations for Gene (Select 26052) - 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 1808981	GRCh37/hg19 1q24.3(chr1:172268908-172389345)x1	DNM3	Copy number loss	not provided	GUncertain significance
Select item 1808980	GRCh37/hg19 1q24.3(chr1:172193303-172244386)x1	DNM3	Copy number loss	not provided	GUncertain significance
Select item 1340417	GRCh37/hg19 1q24.3(chr1:172283167-172322797)x1	DNM3	Copy number loss	not provided	GUncertain significance

Format

Sort by

Choose Destination