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- 16:11, 4 August 2023 Homo sapiens:10q22q23 copy number variation (Ontology Term : 'chromosomal duplication syndrome' added !)
- 16:11, 4 August 2023 Homo sapiens:10q22q23 copy number variation (Ontology Term : 'chromosomal deletion syndrome' added !)
- 16:11, 4 August 2023 Homo sapiens:10q22q23 copy number variation (Ontology Term : 'disease pathway' added !)
- 16:09, 4 August 2023 N Homo sapiens:10q22q23 copy number variation (New pathway)
- 14:11, 4 August 2023 Homo sapiens:11p11.2 copy number variation syndrome (Modified description) (top)
- 14:10, 4 August 2023 Homo sapiens:11p11.2 copy number variation syndrome (Modified description)
- 13:59, 4 August 2023 Homo sapiens:11p11.2 copy number variation syndrome (corrections in progress)
- 12:29, 4 August 2023 Homo sapiens:11p11.2 copy number variation syndrome (correction in progress)
- 12:10, 4 August 2023 Homo sapiens:11p11.2 copy number variation syndrome (correction in progress)
- 17:28, 3 August 2023 Homo sapiens:10q11.21q11.23 copy number variation syndrome (Modified description)
- 17:26, 3 August 2023 Homo sapiens:10q11.21q11.23 copy number variation syndrome (corrections in progress)
- 16:25, 3 August 2023 Homo sapiens:10q11.21q11.23 copy number variation syndrome (correction in progress)
- 14:56, 3 August 2023 Homo sapiens:10q11.21q11.23 copy number variation syndrome (correction in progress)
- 14:40, 3 August 2023 Homo sapiens:10q11.21q11.23 copy number variation syndrome (correction in progress)
- 13:39, 3 August 2023 Homo sapiens:8p23.1 copy number variation syndrome (correction in progress) (top)
- 13:33, 3 August 2023 Homo sapiens:8p23.1 copy number variation syndrome (Modified description)
- 13:32, 3 August 2023 Homo sapiens:8p23.1 copy number variation syndrome (Ontology Term : 'chromosomal deletion syndrome' added !)
- 13:30, 3 August 2023 Homo sapiens:8p23.1 copy number variation syndrome (correction in progress)
- 08:59, 3 August 2023 Homo sapiens:8p23.1 copy number variation syndrome (correction in progress)
- 07:54, 3 August 2023 Homo sapiens:8p23.1 copy number variation syndrome (correction in progress)
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