# PGx CNV Coverage

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

| Gene    | Region Name     | Chromosome          | Start     | End       |
| ------- | --------------- | ------------------- | --------- | --------- |
| GSTM1   | GSTM1           | 1                   | 109687842 | 109693526 |
| UGT2B17 | UGT2B17         | 4                   | 68537222  | 68568499  |
| CYP2E1  | CYP2E1          | 10                  | 133527374 | 133539096 |
| SULT1A1 | SULT1A1         | 16                  | 28603587  | 28613544  |
| 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    |