"Bionano Laboratories"[submitter] AND "DMD"[gene] - ClinVar - NCBI

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Search results

Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 688990	GRCh37/hg19 Xp21.2(chrX:30892354-31250086)x2	DMD, FTHL17 +1 more	Copy number gain	not provided	GUncertain significance
Select item 688900	GRCh37/hg19 Xp21.1(chrX:33183541-33626500)x3	DMD	Copy number gain	not provided	GUncertain significance
Select item 688474	GRCh37/hg19 Xp21.1(chrX:32714173-32787197)x3	DMD	Copy number gain	not provided	GUncertain significance
Select item 688372	GRCh37/hg19 Xp21.1(chrX:32444507-33041454)x3	DMD	Copy number gain	not provided	GUncertain significance
Select item 688137	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1	ARHGAP36, ARHGAP4 +818 more	Copy number loss	not provided	GPathogenic
Select item 687264	GRCh37/hg19 Xp21.1(chrX:31695496-31858935)x2	DMD	Copy number gain	not provided	GUncertain significance
Select item 686970	GRCh37/hg19 Xp22.12-21.1(chrX:20925922-35511818)x1	ACOT9, APOO +42 more	Copy number loss	not provided	GPathogenic
Select item 685565	GRCh37/hg19 Xp22.33-q11.1(chrX:168546-61877279)x1	RBBP7, RBM10 +316 more	Copy number loss	not provided	GPathogenic
Select item 685399	GRCh37/hg19 Xp21.2(chrX:31102254-31157224)x2	DMD	Copy number gain	not provided	GUncertain significance
Select item 685331	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x4	BEX1, BEX2 +818 more	Copy number gain	not provided	GPathogenic
Select item 684976	GRCh37/hg19 Xp21.2-21.1(chrX:31411981-31645888)x3	DMD	Copy number gain	not provided	GUncertain significance
Select item 684963	GRCh37/hg19 Xp22.33-11.4(chrX:168546-38054739)x1	ACE2, ACOT9 +139 more	Copy number loss	not provided	GPathogenic