ClinVar

GRCh37/hg19 16q22.1(chr16:67765964-68246270)x1

Genes:

• DDX28:DEAD-box helicase 28 [Gene - OMIM - HGNC]
• RANBP10:RAN binding protein 10 [Gene - OMIM - HGNC]
• THAP11:THAP domain containing 11 [Gene - OMIM - HGNC]
• CENPT:centromere protein T [Gene - OMIM - HGNC]
• CTRL:chymotrypsin like [Gene - OMIM - HGNC]
• DUS2:dihydrouridine synthase 2 [Gene - OMIM - HGNC]
• DPEP2:dipeptidase 2 [Gene - OMIM - HGNC]
• DPEP3:dipeptidase 3 [Gene - OMIM - HGNC]
• EDC4:enhancer of mRNA decapping 4 [Gene - OMIM - HGNC]
• LCAT:lecithin-cholesterol acyltransferase [Gene - OMIM - HGNC]
• NRN1L:neuritin 1 like [Gene - HGNC]
• NFATC3:nuclear factor of activated T cells 3 [Gene - OMIM - HGNC]
• NUTF2:nuclear transport factor 2 [Gene - OMIM - HGNC]
• PSMB10:proteasome 20S subunit beta 10 [Gene - OMIM - HGNC]
• PSKH1:protein serine kinase H1 [Gene - OMIM - HGNC]
• SLC12A4:solute carrier family 12 member 4 [Gene - OMIM - HGNC]
• TSNAXIP1:translin associated factor X interacting protein 1 [Gene - OMIM - HGNC]

Variant type:

copy number loss

Cytogenetic location:

16q22.1

Genomic location:

Chr16: 67765964 - 68246270 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 16q22.1(chr16:67765964-68246270)x1

HGVS:

NC_000016.9:g.(?_67765964)_(68246270_?)del

This HGVS expression did not pass validation