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GRCh37/hg19 4q13.2(chr4:69049160-69058380)x3 AND See cases

Significance: Likely benign
ClinVar: RCV000447264

Variant: GRCh37/hg19 4q13.2(chr4:69049160-69058380)x3

Type: Variant
Allele: GRCh37/hg19 4q13.2(chr4:69049160-69058380)x3 381989
Gene:
Type: copy number gain
Location: Chr4: 69049160 - 69058380 - assembly GRCh37
References: dbVar: nsv2775999
dbVar: nssv13641665

Condition

PhenotypeInstruction: See cases