GRCh37/hg19 2p25.3(chr2:192760-659746)x3 AND not provided
| Significance: | Likely benign |
|---|---|
| ClinVar: | RCV000682077 |
Variant: GRCh37/hg19 2p25.3(chr2:192760-659746)x3 |
|
| Type: | Variant |
Allele: GRCh37/hg19 2p25.3(chr2:192760-659746)x3 553772 |
|
| Gene: | ACP1 SH3YL1 ALKAL2 |
| Type: | copy number gain |
| Location: |
Chr2: 192760
- 659746
- assembly
GRCh37 |
Condition |
|
| Disease: | not provided |