Related gene-specific medical variations for Gene (Select 171019) - 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 1808408	GRCh37/hg19 5q23.3(chr5:128585033-128985379)x1	ADAMTS19	Copy number loss	not provided	GUncertain significance
Select item 1696725	NM_133638.6(ADAMTS19):c.3313-12986del	ADAMTS19	Deletion (intron variant)	ADAMTS19-associated congenital heartdefect	GUncertain significance
Select item 563107	GRCh37/hg19 5q23.3(chr5:128482655-128948203)x1	ADAMTS19	Copy number loss	not provided	GUncertain significance

Format

Sort by

Choose Destination