ClinVar

GRCh37/hg19 10q24.32-24.33(chr10:103891057-105339973)x1

Genes:

• NT5C2:5'-nucleotidase, cytosolic II [Gene - OMIM - HGNC]
• ARL3:ADP ribosylation factor like GTPase 3 [Gene - OMIM - HGNC]
• ATP5MK:ATP synthase membrane subunit k [Gene - OMIM - HGNC]
• BORCS7:BLOC-1 related complex subunit 7 [Gene - OMIM - HGNC]
• CUEDC2:CUE domain containing 2 [Gene - OMIM - HGNC]
• ELOVL3:ELOVL fatty acid elongase 3 [Gene - OMIM - HGNC]
• FBXL15:F-box and leucine rich repeat protein 15 [Gene - OMIM - HGNC]
• PPRC1:PPARG related coactivator 1 [Gene - OMIM - HGNC]
• SUFU:SUFU negative regulator of hedgehog signaling [Gene - OMIM - HGNC]
• TAF5:TATA-box binding protein associated factor 5 [Gene - OMIM - HGNC]
• WBP1L:WW domain binding protein 1 like [Gene - OMIM - HGNC]
• ACTR1A:actin related protein 1A [Gene - OMIM - HGNC]
• AS3MT:arsenite methyltransferase [Gene - OMIM - HGNC]
• CALHM1:calcium homeostasis modulator 1 [Gene - OMIM - HGNC]
• CALHM3:calcium homeostasis modulator 3 [Gene - OMIM - HGNC]
• CALHM2:calcium homeostasis modulator family member 2 [Gene - OMIM - HGNC]
• C10orf95:chromosome 10 open reading frame 95 [Gene - HGNC]
• CNNM2:cyclin and CBS domain divalent metal cation transport mediator 2 [Gene - OMIM - HGNC]
• CYP17A1:cytochrome P450 family 17 subfamily A member 1 [Gene - OMIM - HGNC]
• GBF1:golgi brefeldin A resistant guanine nucleotide exchange factor 1 [Gene - OMIM - HGNC]
• INA:internexin neuronal intermediate filament protein alpha [Gene - OMIM - HGNC]
• MFSD13A:major facilitator superfamily domain containing 13A [Gene - HGNC]
• MIR146B:microRNA 146b [Gene - OMIM - HGNC]
• NEURL1:neuralized E3 ubiquitin protein ligase 1 [Gene - OMIM - HGNC]
• NFKB2:nuclear factor kappa B subunit 2 [Gene - OMIM - HGNC]
• NOLC1:nucleolar and coiled-body phosphoprotein 1 [Gene - OMIM - HGNC]
• PITX3:paired like homeodomain 3 [Gene - OMIM - HGNC]
• PSD:pleckstrin and Sec7 domain containing [Gene - OMIM - HGNC]
• PCGF6:polycomb group ring finger 6 [Gene - OMIM - HGNC]
• PDCD11:programmed cell death 11 [Gene - OMIM - HGNC]
• SFXN2:sideroflexin 2 [Gene - OMIM - HGNC]
• TRIM8:tripartite motif containing 8 [Gene - OMIM - HGNC]

Variant type:

copy number loss

Cytogenetic location:

10q24.32-24.33

Genomic location:

Chr10: 103891057 - 105339973 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 10q24.32-24.33(chr10:103891057-105339973)x1

HGVS:

NC_000010.10:g.(?_103891057)_(105339973_?)del

This HGVS expression did not pass validation