Related gene-specific medical variations for Gene (Select 7367) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150679	GRCh38/hg38 4q13.2(chr4:68508935-68617567)x3	UGT2B17	Copy number gain	See cases	GLikely benign
Select item 150483	GRCh38/hg38 4q13.2(chr4:68508935-68626378)x3	UGT2B17	Copy number gain	See cases	GLikely benign
Select item 149437	GRCh38/hg38 4q13.2(chr4:68526912-68617567)x1	UGT2B17	Copy number loss	See cases	GLikely benign
Select item 149436	GRCh38/hg38 4q13.2(chr4:68526912-68617567)x3	UGT2B17	Copy number gain	See cases	GLikely benign
Select item 147245	GRCh38/hg38 4q13.2(chr4:68526857-68596407)x3	UGT2B17	Copy number gain	See cases	GBenign
Select item 147117	GRCh38/hg38 4q13.2(chr4:68509451-68568203)x1	UGT2B17	Copy number loss	See cases	GBenign
Select item 147116	GRCh38/hg38 4q13.2(chr4:68509451-68568203)x3	UGT2B17	Copy number gain	See cases	GBenign
Select item 147032	GRCh38/hg38 4q13.2(chr4:68509451-68596407)x1	UGT2B17	Copy number loss	See cases	GBenign
Select item 147031	GRCh38/hg38 4q13.2(chr4:68509451-68596407)x3	UGT2B17	Copy number gain	See cases	GBenign
Select item 147015	GRCh38/hg38 4q13.2(chr4:68509451-68617530)x1	UGT2B17	Copy number loss	See cases	GBenign
Select item 147014	GRCh38/hg38 4q13.2(chr4:68509451-68617530)x3	UGT2B17	Copy number gain	See cases	GBenign
Select item 146955	GRCh38/hg38 4q13.2(chr4:68509452-68617530)x1	UGT2B17	Copy number loss	See cases	GBenign
Select item 146954	GRCh38/hg38 4q13.2(chr4:68509452-68617530)x3	UGT2B17	Copy number gain	See cases	GBenign
Select item 7631	NC_000004.12:g.(68323330_?)_(?_68725531)del	UGT2B17	Deletion	Bone mineral density quantitative trait locus 12	Gassociation