GENETIC ENCYCLOPEDIA
ABOUT US    

   

GRCh37/hg19 1q42.2(chr1:231354205-231372444)x1 AND See cases

Significance: Likely benign
ClinVar: RCV000447271

Variant: GRCh37/hg19 1q42.2(chr1:231354205-231372444)x1

Type: Variant
Allele: GRCh37/hg19 1q42.2(chr1:231354205-231372444)x1 382275
Gene:
Type: copy number loss
Location: Chr1: 231354205 - 231372444 - assembly GRCh37
References: dbVar: nsv2777542
dbVar: nssv13652997

Condition

PhenotypeInstruction: See cases