ClinVar

GRCh37/hg19 17q21.31(chr17:41399892-42125780)x3

Genes:

• ARL4D:ADP ribosylation factor like GTPase 4D [Gene - OMIM - HGNC]
• CD300LG:CD300 molecule like family member g [Gene - OMIM - HGNC]
• CFAP97D1:CFAP97 domain containing 1 [Gene - OMIM - HGNC]
• DHX8:DEAH-box helicase 8 [Gene - OMIM - HGNC]
• ETV4:ETS variant transcription factor 4 [Gene - OMIM - HGNC]
• LSM12:LSM12 homolog [Gene - OMIM - HGNC]
• MPP2:MAGUK p55 scaffold protein 2 [Gene - OMIM - HGNC]
• MPP3:MAGUK p55 scaffold protein 3 [Gene - OMIM - HGNC]
• NAGS:N-acetylglutamate synthase [Gene - OMIM - HGNC]
• DUSP3:dual specificity phosphatase 3 [Gene - OMIM - HGNC]
• MEOX1:mesenchyme homeobox 1 [Gene - OMIM - HGNC]
• PPY:pancreatic polypeptide [Gene - OMIM - HGNC]
• PYY:peptide YY [Gene - OMIM - HGNC]
• SOST:sclerostin [Gene - OMIM - HGNC]
• TMEM101:transmembrane protein 101 [Gene - HGNC]

Variant type:

copy number gain

Cytogenetic location:

17q21.31

Genomic location:

Chr17: 41399892 - 42125780 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 17q21.31(chr17:41399892-42125780)x3

HGVS:

This HGVS expression did not pass validation