Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv3152 | Chr2:213282926 - 213332692 on Build GRCh38 | Insertion | SPAG16 LOC100130451 |
nsv1013206 | Chr2:213267855 - 213302172 on Build GRCh38 | Loss | SPAG16 LOC100130451 |
nsv834531 | Chr2:213250900 - 213437519 on Build GRCh38 | Loss | SPAG16 LOC100130451 |