Related gene-specific medical variations for Gene (Select 3983) - 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 2365309	NM_002313.7(ABLIM1):c.991G>A (p.Val331Ile)	ABLIM1, LOC126861051 (V271I +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 686791	GRCh37/hg19 10q25.3(chr10:116322646-116572153)x3	ABLIM1	Copy number gain	not provided	GUncertain significance
Select item 563722	GRCh37/hg19 10q25.3(chr10:116322646-116572153)x3	ABLIM1	Copy number gain	not provided	GLikely benign

Format

Sort by

Choose Destination