ClinVar

GRCh37/hg19 20q13.33(chr20:62141508-62405797)x3

Genes:

• ARFRP1:ADP ribosylation factor related protein 1 [Gene - OMIM - HGNC]
• LIME1:Lck interacting transmembrane adaptor 1 [Gene - OMIM - HGNC]
• SLC2A4RG:SLC2A4 regulator [Gene - OMIM - HGNC]
• TNFRSF6B:TNF receptor superfamily member 6b [Gene - OMIM - HGNC]
• FNDC11:fibronectin type III domain containing 11 [Gene - HGNC]
• GMEB2:glucocorticoid modulatory element binding protein 2 [Gene - OMIM - HGNC]
• HELZ2:helicase with zinc finger 2 [Gene - OMIM - HGNC]
• PPDPF:pancreatic progenitor cell differentiation and proliferation factor [Gene - HGNC]
• PTK6:protein tyrosine kinase 6 [Gene - OMIM - HGNC]
• RTEL1:regulator of telomere elongation helicase 1 [Gene - OMIM - HGNC]
• SRMS:src-related kinase lacking C-terminal regulatory tyrosine and N-terminal myristylation sites [Gene - OMIM - HGNC]
• STMN3:stathmin 3 [Gene - OMIM - HGNC]
• ZGPAT:zinc finger CCCH-type and G-patch domain containing [Gene - OMIM - HGNC]
• ZBTB46:zinc finger and BTB domain containing 46 [Gene - OMIM - HGNC]

Variant type:

copy number gain

Cytogenetic location:

20q13.33

Genomic location:

Chr20: 62141508 - 62405797 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 20q13.33(chr20:62141508-62405797)x3

HGVS:

This HGVS expression did not pass validation