1q21.1 duplication variant
Evidence from:
primary |
all sources
Related entities (4)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| 1q21.1 duplication | associated_with | bipolar disorder | — | 1 |
| 1q21.1 duplication | associated_with | epilepsy | — | 1 |
| 1q21.1 duplication | associated_with | head size | — | 1 |
| 1q21.1 duplication | associated_with | psychiatric traits | — | 1 |
Mentioned in (5)
Papers in which this entity is mentioned.
- Diminishing return for increased Mappability with longer sequencing reads: implications of the k-mer distributions in the human genome. (2014)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
- High frequencies of de novo CNVs in bipolar disorder and schizophrenia. (2011)
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
- A syndrome of short stature, microcephaly and speech delay is associated with duplications reciprocal to the common Sotos syndrome deletion. (2010)
Merged raw entities (4)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| 1q21.1 duplication | variant | 5 | 9 |
| 1q21.1 cnv duplication | variant | — | — |
| 1q21.1 dup | variant | — | — |
| duplication at 1q21.1 | variant | — | — |