SNHG14[gene] and "single gene"[properties] - 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 149460	GRCh38/hg38 15q11.2(chr15:25087769-25088727)x1	SNHG14	Copy number loss	See cases	GLikely benign
Select item 150221	GRCh38/hg38 15q11.2(chr15:25087994-25088727)x1	SNHG14	Copy number loss	See cases	GLikely benign
Select item 150219	GRCh38/hg38 15q11.2(chr15:25087994-25088727)x3	SNHG14	Copy number gain	See cases	GLikely benign
Select item 2498602	NC_000015.10:g.25278417C>T	SNHG14	Single nucleotide variant	not provided	GLikely benign

Format

Sort by

Choose Destination