Related gene-specific medical variations for Gene (Select 57691) - 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 545337	NC_000006.12:g.(?_57046622)_(57088889_?)del	KIAA1586	Deletion	Schizophrenia	GLikely pathogenic
Select item 144905	GRCh38/hg38 6p12.1(chr6:57052810-57085760)x1	KIAA1586	Copy number loss	See cases	GLikely benign
Select item 144904	GRCh38/hg38 6p12.1(chr6:57052810-57085760)x4	KIAA1586	Copy number gain	See cases	GLikely benign
Select item 144903	GRCh38/hg38 6p12.1(chr6:57052810-57085760)x3	KIAA1586	Copy number gain	See cases	GBenign/Likely benign

Format

Sort by

Choose Destination