Submitter |
RCV |
SCV |
Clinical significance |
Condition |
Last evaluated |
Review status |
Method |
Comment |
Baylor Genetics |
RCV000767554 |
SCV000898176 |
likely pathogenic |
not provided |
2018-11-01 |
criteria provided, single submitter |
clinical testing |
Deletions involving this region have been previously reported in patients with developmental delay and autism (PMID: 23657883) |
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