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. 2020 Sep 17;49(D1):D1218–D1224. doi: 10.1093/nar/gkaa753

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© The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 1. — Statistics of human infertility genes and chromosomal abnormalities in the IDDB 2020. (A) The intersection of infertility genes between females and males. (B) The intersection of chromosomal abnormalities between aneuploidies and structural variants. (C) Schematic representation of the chromosomal location of human infertility-associated genes leads to human infertility disease. (D) Top 10 mutated human infertility-associated genes calculated by unique pathogenic variants for each gene. (E) Statistics of protein variants collected from infertility patients’ samples in the IDDB 2020.