ClinVar

GRCh37/hg19 10q26.3(chr10:131398569-135427143)x1

Genes:

• ADAM8:ADAM metallopeptidase domain 8 [Gene - OMIM - HGNC]
• BNIP3:BCL2 interacting protein 3 [Gene - OMIM - HGNC]
• EBF3:EBF transcription factor 3 [Gene - OMIM - HGNC]
• JAKMIP3:Janus kinase and microtubule interacting protein 3 [Gene - OMIM - HGNC]
• NKX6-2:NK6 homeobox 2 [Gene - OMIM - HGNC]
• MGMT:O-6-methylguanine-DNA methyltransferase [Gene - OMIM - HGNC]
• PWWP2B:PWWP domain containing 2B [Gene - HGNC]
• TCERG1L-AS1:TCERG1L antisense RNA 1 [Gene - HGNC]
• VENTX:VENT homeobox [Gene - OMIM - HGNC]
• ADGRA1:adhesion G protein-coupled receptor A1 [Gene - OMIM - HGNC]
• CALY:calcyon neuron specific vesicular protein [Gene - OMIM - HGNC]
• CFAP46:cilia and flagella associated protein 46 [Gene - OMIM - HGNC]
• CYP2E1:cytochrome P450 family 2 subfamily E member 1 [Gene - OMIM - HGNC]
• DPYSL4:dihydropyrimidinase like 4 [Gene - OMIM - HGNC]
• ECHS1:enoyl-CoA hydratase, short chain 1 [Gene - OMIM - HGNC]
• FUOM:fucose mutarotase [Gene - OMIM - HGNC]
• GLRX3:glutaredoxin 3 [Gene - OMIM - HGNC]
• INPP5A:inositol polyphosphate-5-phosphatase A [Gene - OMIM - HGNC]
• KNDC1:kinase non-catalytic C-lobe domain containing 1 [Gene - OMIM - HGNC]
• LRRC27:leucine rich repeat containing 27 [Gene - HGNC]
• LINC01166:long intergenic non-protein coding RNA 1166 [Gene - HGNC]
• LINC02870:long intergenic non-protein coding RNA 2870 [Gene - HGNC]
• MTG1:mitochondrial ribosome associated GTPase 1 [Gene - HGNC]
• PAOX:polyamine oxidase [Gene - OMIM - HGNC]
• PRAP1:proline rich acidic protein 1 [Gene - OMIM - HGNC]
• PPP2R2D:protein phosphatase 2 regulatory subunit Bdelta [Gene - OMIM - HGNC]
• STK32C:serine/threonine kinase 32C [Gene - HGNC]
• SPRN:shadow of prion protein [Gene - OMIM - HGNC]
• SYCE1:synaptonemal complex central element protein 1 [Gene - OMIM - HGNC]
• TCERG1L:transcription elongation regulator 1 like [Gene - OMIM - HGNC]
• TUBGCP2:tubulin gamma complex component 2 [Gene - OMIM - HGNC]
• UTF1:undifferentiated embryonic cell transcription factor 1 [Gene - OMIM - HGNC]
• ZNF511:zinc finger protein 511 [Gene - HGNC]

Variant type:

copy number loss

Cytogenetic location:

10q26.3

Genomic location:

Chr10: 131398569 - 135427143 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 10q26.3(chr10:131398569-135427143)x1

HGVS:

This HGVS expression did not pass validation

Observations:

1