ClinVar

GRCh37/hg19 16p13.3(chr16:2188712-2580690)x4

Genes:

• ABCA3:ATP binding cassette subfamily A member 3 [Gene - OMIM - HGNC]
• ATP6V0C:ATPase H+ transporting V0 subunit c [Gene - OMIM - HGNC]
• BRICD5:BRICHOS domain containing 5 [Gene - HGNC]
• CASKIN1:CASK interacting protein 1 [Gene - OMIM - HGNC]
• E4F1:E4F transcription factor 1 [Gene - OMIM - HGNC]
• MLST8:MTOR associated protein, LST8 homolog [Gene - OMIM - HGNC]
• RAB26:RAB26, member RAS oncogene family [Gene - OMIM - HGNC]
• RNPS1:RNA binding protein with serine rich domain 1 [Gene - OMIM - HGNC]
• TBC1D24:TBC1 domain family member 24 [Gene - OMIM - HGNC]
• TRAF7:TNF receptor associated factor 7 [Gene - OMIM - HGNC]
• AMDHD2:amidohydrolase domain containing 2 [Gene - HGNC]
• CEMP1:cementum protein 1 [Gene - OMIM - HGNC]
• CCNF:cyclin F [Gene - OMIM - HGNC]
• DNASE1L2:deoxyribonuclease 1 like 2 [Gene - OMIM - HGNC]
• ECI1:enoyl-CoA delta isomerase 1 [Gene - OMIM - HGNC]
• NTN3:netrin 3 [Gene - OMIM - HGNC]
• PGP:phosphoglycolate phosphatase [Gene - OMIM - HGNC]
• TEDC2:tubulin epsilon and delta complex 2 [Gene - HGNC]

Variant type:

copy number gain

Cytogenetic location:

16p13.3

Genomic location:

Chr16: 2188712 - 2580690 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 16p13.3(chr16:2188712-2580690)x4

HGVS:

This HGVS expression did not pass validation