GENETIC ENCYCLOPEDIA
ABOUT US    

   

GRCh37/hg19 6q13-14.2(chr6:73674612-84829774)x1 AND not provided

Significance: Pathogenic
ClinVar: RCV000682681

Variant: GRCh37/hg19 6q13-14.2(chr6:73674612-84829774)x1

Type: Variant
Allele: GRCh37/hg19 6q13-14.2(chr6:73674612-84829774)x1 554376
Gene:
Type: copy number loss
Location: Chr6: 73674612 - 84829774 - assembly GRCh37

Condition

Disease: not provided