Fig. 5From: A novel 268 kb deletion combined with a splicing variant in IL7R causes of severe combined immunodeficiency in a Chinese family: a case reportDistribution of IL7R domains and all likely pathogenic and pathogenic variants associated with SCID in ClinVar database. The reported variants are indicated in red (https://www.ncbi.nlm.nih.gov/clinvar/, the last access time was October 4, 2023)Back to article page