PGx CNV Coverage

Copy number variation can be detected for genes and regions listed below. The chromosome locations are GRCh38 based.

GeneRegion NameChromosomeStartEnd

GSTM1

GSTM1

1

109687842

109693526

UGT2B17

UGT2B17

4

68537222

68568499

CYP2E1

CYP2E1

10

133527374

133539096

SULT1A1

SULT1A1

16

28615068

28623382

CYP2A6

CYP2A6.intron.7

19

40844791

40845293

CYP2A6

CYP2A6.exon.1

19

40850267

40850414

CYP2D6

CYP2D6.exon.9

22

42126498

42126752

CYP2D6

CYP2D6.intron.2

22

42129188

42129734

CYP2D6

CYP2D6.p5

22

42130886

42131379

GSTT1

GSTT1

22_KI270879v1_alt

270316

278477

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