Small insertions and deletions (INDELs) in human genomes.

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PyRAD: assembly of de novo RADseq loci for phylogenetic analyses (2013, background): “Indel variation is common even within a single species (Mullaney et al. , 2010) and thus it should be no surprise that restriction site associated libraries often sample regions containing such variation.”
Protein design and variant prediction using autoregressive generative models (2021, background): “Indels make up 15 – 21% of human polymorphisms 41 – 43 , 44% of human proteins contain disordered regions longer than 30 amino acids 40,44 , and both are enriched in association with human diseases such as cystic ﬁ brosis, many cancers 45,46 , cardiovascular and neurodegenerative diseases, and…”
PolymiRTS Database 3.0: linking polymorphisms in microRNAs and their target sites with human diseases and biological pathways (2013, background): “About 18% of known human genetic variants are INDELs (27,28), constituting the second largest class of genetic variants after SNPs.”
SvABA: genome-wide detection of structural variants and indels by local assembly (2018, background): “sized events between 10 bp and 10 kbp are the primary source of structural variation (Mullaney et al. 2010).”