WP5352 - 10q11.21q11.23 copy number variation syndrome - Homo sapiens
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https://www.ndexbio.org/viewer/networks/ecb98337-1438-11f0-9806-005056ae3c32
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资源简介：
10q11.21q11.23 copy number variation (CNV) syndrome is a rare genetic disorder caused by a deletion or duplication of genetic material on chromosome 10. The exact genetic location chr10:49,390,199-51,058,796 (GRCh37) was taken from Kirov et al. 2014 and literature cited there.
创建时间：
2025-04-17
