Related gene-specific medical variations for Gene (Select 25769) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809313	GRCh37/hg19 9p22.1(chr9:19558806-19625173)x1	SLC24A2	Copy number loss	not provided	GUncertain significance
Select item 815244	GRCh37/hg19 9p22.1-21.3(chr9:19686451-19959038)x1	SLC24A2	Copy number loss	not provided	GUncertain significance
Select item 563575	GRCh37/hg19 9p22.1(chr9:19604951-19684827)x1	SLC24A2	Copy number loss	not provided	GUncertain significance
Select item 547114	GRCh37/hg19 9p22.1-21.3(chr9:19630553-20096994)x3	SLC24A2	Copy number gain	not provided	GLikely benign
Select item 221725	GRCh38/hg38 9p22.1(chr9:19678271-19779174)x1	SLC24A2	Copy number loss	Premature ovarian failure	GBenign

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