ClinVar

GRCh37/hg19 5q34-35.1(chr5:166378793-170174830)x1

Genes:

• WWC1:WW and C2 domain containing 1 [Gene - OMIM - HGNC]
• RARS1:arginyl-tRNA synthetase 1 [Gene - OMIM - HGNC]
• C5orf58:chromosome 5 open reading frame 58 [Gene - HGNC]
• DOCK2:dedicator of cytokinesis 2 [Gene - OMIM - HGNC]
• FOXI1:forkhead box I1 [Gene - OMIM - HGNC]
• INSYN2B:inhibitory synaptic factor family member 2B [Gene - HGNC]
• LCP2:lymphocyte cytosolic protein 2 [Gene - OMIM - HGNC]
• MIR103A1:microRNA 103a-1 [Gene - OMIM - HGNC]
• PANK3:pantothenate kinase 3 [Gene - OMIM - HGNC]
• KCNMB1:potassium calcium-activated channel subfamily M regulatory beta subunit 1 [Gene - OMIM - HGNC]
• KCNIP1:potassium voltage-gated channel interacting protein 1 [Gene - OMIM - HGNC]
• SLIT3:slit guidance ligand 3 [Gene - OMIM - HGNC]
• SPDL1:spindle apparatus coiled-coil protein 1 [Gene - OMIM - HGNC]
• TENM2:teneurin transmembrane protein 2 [Gene - OMIM - HGNC]
• LOC100128059:uncharacterized LOC100128059 [Gene]

Variant type:

copy number loss

Cytogenetic location:

5q34-35.1

Genomic location:

Chr5: 166378793 - 170174830 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 5q34-35.1(chr5:166378793-170174830)x1

HGVS:

NC_000005.9:g.(?_166378793)_(170174830_?)del

This HGVS expression did not pass validation