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• 19:23, 8 August 2023 Homo sapiens:15q25 copy number variation‎ (Ontology Term : 'chromosome 15q25 deletion syndrome' added !)
• 19:23, 8 August 2023 Homo sapiens:15q25 copy number variation‎ (Ontology Term : 'disease pathway' added !)
• 19:22, 8 August 2023 Homo sapiens:15q25 copy number variation‎ (Modified description)
• 19:19, 8 August 2023 N Homo sapiens:15q25 copy number variation‎ (New pathway)
• 08:31, 8 August 2023 Homo sapiens:15q11q13 copy number variation‎ (Ontology Term : 'chromosomal duplication syndrome' added !)
• 08:31, 8 August 2023 Homo sapiens:15q11q13 copy number variation‎ (Ontology Term : 'chromosomal deletion syndrome' added !)
• 08:30, 8 August 2023 Homo sapiens:15q11q13 copy number variation‎ (Ontology Term : 'disease pathway' added !)
• 08:28, 8 August 2023 Homo sapiens:15q11q13 copy number variation‎ (Modified description)
• 08:21, 8 August 2023 N Homo sapiens:15q11q13 copy number variation‎ (New pathway)
• 15:16, 7 August 2023 Homo sapiens:Prader-Willi and Angelman syndrome‎ (legend correction)
• 15:12, 7 August 2023 Homo sapiens:Prader-Willi and Angelman syndrome‎ (Modified description)
• 15:09, 7 August 2023 Homo sapiens:Prader-Willi and Angelman syndrome‎ (Modified description)
• 15:07, 7 August 2023 Homo sapiens:Prader-Willi and Angelman syndrome‎ (update)
• 10:31, 7 August 2023 Homo sapiens:Prader-Willi and Angelman syndrome‎ (update)
• 10:03, 7 August 2023 Homo sapiens:13q12.12 copy number variation‎ (Ontology Term : 'chromosomal duplication syndrome' added !)
• 10:03, 7 August 2023 Homo sapiens:13q12.12 copy number variation‎ (Ontology Term : 'chromosomal deletion syndrome' added !)
• 10:03, 7 August 2023 Homo sapiens:13q12.12 copy number variation‎ (Ontology Term : 'disease pathway' added !)
• 10:00, 7 August 2023 Homo sapiens:13q12.12 copy number variation‎ (Modified description)
• 09:55, 7 August 2023 N Homo sapiens:13q12.12 copy number variation‎ (New pathway)
• 13:49, 6 August 2023 Homo sapiens:13q12 or CRYL1 copy number variation ‎ (Ontology Term : 'chromosomal duplication syndrome' added !)
• 13:49, 6 August 2023 Homo sapiens:13q12 or CRYL1 copy number variation ‎ (Ontology Term : 'chromosomal deletion syndrome' added !)
• 13:49, 6 August 2023 Homo sapiens:13q12 or CRYL1 copy number variation ‎ (Ontology Term : 'PW:0000001' removed !)
• 13:49, 6 August 2023 Homo sapiens:13q12 or CRYL1 copy number variation ‎ (Ontology Term : 'disease pathway' added !)
• 13:49, 6 August 2023 Homo sapiens:13q12 or CRYL1 copy number variation ‎ (Ontology Term : 'Pathway Ontology' added !)
• 13:47, 6 August 2023 N Homo sapiens:13q12 or CRYL1 copy number variation ‎ (New pathway)
• 13:21, 6 August 2023 Homo sapiens:10q22q23 copy number variation‎ (Modified description)
• 13:20, 6 August 2023 Homo sapiens:10q22q23 copy number variation‎ (Modified description)
• 13:11, 6 August 2023 Homo sapiens:10q22q23 copy number variation‎ (progress save)
• 12:56, 6 August 2023 Homo sapiens:10q22q23 copy number variation‎ (work in progress)
• 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)
• 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)
• 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)
• 16:07, 2 August 2023 Homo sapiens:8p23.1 copy number variation syndrome‎ (correction in progress)

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