ClinVar

GRCh37/hg19 1p36.21-36.13(chr1:16096742-16725355)x1

Genes:

• EPHA2:EPH receptor A2 [Gene - OMIM - HGNC]
• FBXO42:F-box protein 42 [Gene - OMIM - HGNC]
• ARHGEF19:Rho guanine nucleotide exchange factor 19 [Gene - OMIM - HGNC]
• SZRD1:SUZ RNA binding domain containing 1 [Gene - HGNC]
• CLCNKA:chloride voltage-gated channel Ka [Gene - OMIM - HGNC]
• CLCNKB:chloride voltage-gated channel Kb [Gene - OMIM - HGNC]
• CPLANE2:ciliogenesis and planar polarity effector complex subunit 2 [Gene - HGNC]
• FAM131C:family with sequence similarity 131 member C [Gene - HGNC]
• FBLIM1:filamin binding LIM protein 1 [Gene - OMIM - HGNC]
• HSPB7:heat shock protein family B (small) member 7 [Gene - OMIM - HGNC]
• SPEN:spen family transcriptional repressor [Gene - OMIM - HGNC]
• SPATA21:spermatogenesis associated 21 [Gene - HGNC]
• SRARP:steroid receptor associated and regulated protein [Gene - OMIM - HGNC]
• ZBTB17:zinc finger and BTB domain containing 17 [Gene - OMIM - HGNC]

Variant type:

copy number loss

Cytogenetic location:

1p36.21-36.13

Genomic location:

Chr1: 16096742 - 16725355 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 1p36.21-36.13(chr1:16096742-16725355)x1

HGVS:

NC_000001.10:g.(?_16096742)_(16725355_?)del

This HGVS expression did not pass validation