Related gene-specific medical variations for Gene (Select 26037) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1340904	GRCh37/hg19 14q24.2(chr14:71941404-72026183)x1	SIPA1L1	Copy number loss	not provided	GUncertain significance
Select item 685278	GRCh37/hg19 14q24.2(chr14:71965046-72045983)x1	SIPA1L1	Copy number loss	not provided	GUncertain significance
Select item 564097	GRCh37/hg19 14q24.2(chr14:71969845-72114494)x1	SIPA1L1	Copy number loss	not provided	GUncertain significance
Select item 151223	GRCh38/hg38 14q24.2(chr14:71696770-71749145)x3	SIPA1L1	Copy number gain	See cases	GLikely benign

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