Related gene-specific medical variations for Gene (Select 339479) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 979927	GRCh37/hg19 1q31.1-31.2(chr1:190098893-192114806)x1	BRINP3	Copy number loss	not provided	GUncertain significance
Select item 979317	GRCh37/hg19 1q31.1-31.2(chr1:189776412-191289591)x3	BRINP3	Copy number gain	not provided	GUncertain significance
Select item 979316	GRCh37/hg19 1q31.1(chr1:190226030-190304397)x1	BRINP3	Copy number loss	not provided	GUncertain significance
Select item 979315	GRCh37/hg19 1q31.1(chr1:190184943-190361454)x1	BRINP3	Copy number loss	not provided	GUncertain significance
Select item 814152	GRCh37/hg19 1q31.1(chr1:190186386-190675536)x3	BRINP3	Copy number gain	not provided	GUncertain significance
Select item 814151	GRCh37/hg19 1q31.1(chr1:190161138-190304397)x1	BRINP3	Copy number loss	not provided	GUncertain significance
Select item 688229	GRCh37/hg19 1q31.1(chr1:190177709-190356910)x1	BRINP3	Copy number loss	not provided	GUncertain significance
Select item 684545	Single allele	BRINP3	Deletion	not provided	Gnot provided
Select item 565206	GRCh37/hg19 1q31.1(chr1:189547624-190142512)x3	BRINP3	Copy number gain	not provided	GUncertain significance

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