ClinVar

GRCh37/hg19 20q13.33(chr20:62576747-62915555)x3

Genes:

• LKAAEAR1:LKAAEAR motif containing 1 [Gene - HGNC]
• SOX18:SRY-box transcription factor 18 [Gene - OMIM - HGNC]
• MYT1:myelin transcription factor 1 [Gene - OMIM - HGNC]
• NPBWR2:neuropeptides B and W receptor 2 [Gene - OMIM - HGNC]
• OPRL1:opioid related nociceptin receptor 1 [Gene - OMIM - HGNC]
• PRPF6:pre-mRNA processing factor 6 [Gene - OMIM - HGNC]
• PCMTD2:protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 2 [Gene - HGNC]
• RGS19:regulator of G protein signaling 19 [Gene - OMIM - HGNC]
• SAMD10:sterile alpha motif domain containing 10 [Gene - HGNC]
• TCEA2:transcription elongation factor A2 [Gene - OMIM - HGNC]
• UCKL1:uridine-cytidine kinase 1 like 1 [Gene - OMIM - HGNC]
• ZNF512B:zinc finger protein 512B [Gene - OMIM - HGNC]

Variant type:

copy number gain

Cytogenetic location:

20q13.33

Genomic location:

Chr20: 62576747 - 62915555 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 20q13.33(chr20:62576747-62915555)x3

HGVS:

This HGVS expression did not pass validation