ClinVar

GRCh37/hg19 18q22.3-23(chr18:72453821-78014123)x1

Genes:

• ADNP2:ADNP homeobox 2 [Gene - OMIM - HGNC]
• ATP9B:ATPase phospholipid transporting 9B (putative) [Gene - OMIM - HGNC]
• CTDP1:CTD phosphatase subunit 1 [Gene - OMIM - HGNC]
• GALR1:galanin receptor 1 [Gene - OMIM - HGNC]
• HSBP1L1:heat shock factor binding protein 1 like 1 [Gene - HGNC]
• LINC01879:long intergenic non-protein coding RNA 1879 [Gene - HGNC]
• LINC00683:long intergenic non-protein coding RNA 683 [Gene - HGNC]
• MBP:myelin basic protein [Gene - OMIM - HGNC]
• NFATC1:nuclear factor of activated T cells 1 [Gene - OMIM - HGNC]
• PARD6G:par-6 family cell polarity regulator gamma [Gene - OMIM - HGNC]
• KCNG2:potassium voltage-gated channel modifier subfamily G member 2 [Gene - OMIM - HGNC]
• PTGR3:prostaglandin reductase 3 [Gene - OMIM - HGNC]
• RBFA:ribosome binding factor A [Gene - OMIM - HGNC]
• SMIM21:small integral membrane protein 21 [Gene - HGNC]
• SLC66A2:solute carrier family 66 member 2 [Gene - HGNC]
• SALL3:spalt like transcription factor 3 [Gene - OMIM - HGNC]
• TSHZ1:teashirt zinc finger homeobox 1 [Gene - OMIM - HGNC]
• TXNL4A:thioredoxin like 4A [Gene - OMIM - HGNC]
• ZNF236:zinc finger protein 236 [Gene - OMIM - HGNC]
• ZNF407:zinc finger protein 407 [Gene - OMIM - HGNC]
• ZNF516:zinc finger protein 516 [Gene - OMIM - HGNC]

Variant type:

copy number loss

Cytogenetic location:

18q22.3-23

Genomic location:

Chr18: 72453821 - 78014123 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 18q22.3-23(chr18:72453821-78014123)x1

HGVS:

This HGVS expression did not pass validation

Observations:

1