ClinVar

GRCh37/hg19 6p25.3-25.1(chr6:204009-6447311)x1

Genes:

• GMDS:GDP-mannose 4,6-dehydratase [Gene - OMIM - HGNC]
• HUS1B:HUS1 checkpoint clamp component B [Gene - OMIM - HGNC]
• LYRM4:LYR motif containing 4 [Gene - OMIM - HGNC]
• NQO2:N-ribosyldihydronicotinamide:quinone reductase 2 [Gene - OMIM - HGNC]
• PXDC1:PX domain containing 1 [Gene - HGNC]
• WRNIP1:WRN helicase interacting protein 1 [Gene - OMIM - HGNC]
• BPHL:biphenyl hydrolase like [Gene - OMIM - HGNC]
• CDYL:chromodomain Y like [Gene - OMIM - HGNC]
• C6orf201:chromosome 6 open reading frame 201 [Gene - HGNC]
• F13A1:coagulation factor XIII A chain [Gene - OMIM - HGNC]
• DUSP22:dual specificity phosphatase 22 [Gene - OMIM - HGNC]
• ECI2:enoyl-CoA delta isomerase 2 [Gene - OMIM - HGNC]
• EXOC2:exocyst complex component 2 [Gene - OMIM - HGNC]
• FAM217A:family with sequence similarity 217 member A [Gene - HGNC]
• FAM50B:family with sequence similarity 50 member B [Gene - OMIM - HGNC]
• FOXC1:forkhead box C1 [Gene - OMIM - HGNC]
• FOXF2:forkhead box F2 [Gene - OMIM - HGNC]
• FOXQ1:forkhead box Q1 [Gene - OMIM - HGNC]
• IRF4:interferon regulatory factor 4 [Gene - OMIM - HGNC]
• LINC01600:long intergenic non-protein coding RNA 1600 [Gene - HGNC]
• MYLK4:myosin light chain kinase family member 4 [Gene - HGNC]
• NRN1:neuritin 1 [Gene - OMIM - HGNC]
• FARS2:phenylalanyl-tRNA synthetase 2, mitochondrial [Gene - OMIM - HGNC]
• PRPF4B:pre-mRNA processing factor 4B [Gene - OMIM - HGNC]
• PSMG4:proteasome assembly chaperone 4 [Gene - OMIM - HGNC]
• PPP1R3G:protein phosphatase 1 regulatory subunit 3G [Gene - OMIM - HGNC]
• RIPK1:receptor interacting serine/threonine kinase 1 [Gene - OMIM - HGNC]
• RPP40:ribonuclease P/MRP subunit p40 [Gene - OMIM - HGNC]
• SERPINB1:serpin family B member 1 [Gene - OMIM - HGNC]
• SERPINB6:serpin family B member 6 [Gene - OMIM - HGNC]
• SERPINB9:serpin family B member 9 [Gene - OMIM - HGNC]
• SLC22A23:solute carrier family 22 member 23 [Gene - OMIM - HGNC]
• TUBB2A:tubulin beta 2A class IIa [Gene - OMIM - HGNC]
• TUBB2B:tubulin beta 2B class IIb [Gene - OMIM - HGNC]
• KU-MEL-3:uncharacterized LOC497048 [Gene]

Variant type:

copy number loss

Cytogenetic location:

6p25.3-25.1

Genomic location:

Chr6: 204009 - 6447311 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 6p25.3-25.1(chr6:204009-6447311)x1

HGVS:

NC_000006.11:g.(?_204009)_(6447311_?)del

This HGVS expression did not pass validation