LOC113743971[gene] and "single gene"[properties] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150099	GRCh38/hg38 7q36.3(chr7:159214229-159335865)x3	LOC113743971	Copy number gain	See cases	GLikely benign
Select item 148488	GRCh38/hg38 7q36.3(chr7:159214359-159335866)x3	LOC113743971	Copy number gain	See cases	GLikely benign
Select item 146833	GRCh38/hg38 7q36.3(chr7:159296711-159332897)x1	LOC113743971	Copy number loss	See cases	GBenign

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