Related gene-specific medical variations for Gene (Select 57536) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1340664	GRCh37/hg19 18q12.2(chr18:34527570-34593436)x1	KIAA1328	Copy number loss	not provided	GLikely benign
Select item 979692	GRCh37/hg19 18q12.2(chr18:34469881-34714860)x1	KIAA1328	Copy number loss	not provided	GLikely benign
Select item 816001	GRCh37/hg19 18q12.2(chr18:34527569-34586983)x1	KIAA1328	Copy number loss	not provided	GLikely benign
Select item 816000	GRCh37/hg19 18q12.2(chr18:34499368-34571724)x1	KIAA1328	Copy number loss	not provided	GUncertain significance
Select item 564489	GRCh37/hg19 18q12.2(chr18:34586292-34755502)x1	KIAA1328	Copy number loss	not provided	GUncertain significance
Select item 226266	GRCh37/hg19 18q12.2(chr18:34546490-34698627)	KIAA1328	Copy number loss	Abnormal esophagus morphology	GLikely benign

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