GENETIC ENCYCLOPEDIA
ABOUT US    

   

GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 AND See cases

Significance: Pathogenic
ClinVar: RCV000511289

Variant: GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3

Type: Variant
Allele: GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 437160
Gene:
Type: copy number gain
Location: Chr19: 260912 - 58956888 - assembly GRCh37
References: dbVar: nsv2779094
dbVar: nssv13639328

Condition

PhenotypeInstruction: See cases