GENETIC ENCYCLOPEDIA
ABOUT US    

   

GRCh37/hg19 2p16.1(chr2:58190764-58386590)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000447233

Variant: GRCh37/hg19 2p16.1(chr2:58190764-58386590)x3

Type: Variant
Allele: GRCh37/hg19 2p16.1(chr2:58190764-58386590)x3 380755
Gene:
Type: copy number gain
Location: Chr2: 58190764 - 58386590 - assembly GRCh37
References: dbVar: nsv2769151
dbVar: nssv13653309

Condition

PhenotypeInstruction: See cases