"GeneDx"[submitter] AND "BDNF"[gene] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58858	GRCh38/hg38 11p14.3-12(chr11:22550115-38199159)x1	PAX6_HS3, PAX6_HS8 +334 more	Copy number loss	See cases	GPathogenic
Select item 145969	GRCh38/hg38 11p14.2-13(chr11:26368962-35252976)x1	LOC129390275, LOC129390276 +255 more	Copy number loss	See cases	GPathogenic
Select item 1260492	NM_001709.5(BDNF):c.-21-1064CA[11]	BDNF, BDNF-AS	Microsatellite (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1258199	NM_001709.5(BDNF):c.-21-1044G>C	BDNF, BDNF-AS	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1224644	NM_001709.5(BDNF):c.-21-1064CA[13]	BDNF, BDNF-AS	Microsatellite (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1287138	NM_001709.5(BDNF):c.-21-1065G>A	BDNF, BDNF-AS	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1287949	NM_001709.5(BDNF):c.-21-1256G>A	BDNF, BDNF-AS	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1287893	NM_001709.5(BDNF):c.-21-15304=	BDNF, BDNF-AS	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238836	NM_001709.5(BDNF):c.-21-15332T>C	BDNF-AS, BDNF	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 503514	NM_001709.5(BDNF):c.-21-15685_-21-15684del	BDNF, BDNF-AS (S6fs)	Deletion (frameshift variant +2 more)	not specified	GUncertain significance
Select item 1276343	NM_001709.5(BDNF):c.-21-15778G>T	BDNF, BDNF-AS	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 253976	GRCh37/hg19 11p14.1(chr11:27407012-28000144)x3	LIN7C, BDNF +2 more	Copy number gain	See cases	GUncertain significance