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GRCh37/hg19 13q12.11(chr13:20208069-20436518)x3 AND See cases

Significance: Likely benign
ClinVar: RCV000447276

Variant: GRCh37/hg19 13q12.11(chr13:20208069-20436518)x3

Type: Variant
Allele: GRCh37/hg19 13q12.11(chr13:20208069-20436518)x3 381820
Gene:
Type: copy number gain
Location: Chr13: 20208069 - 20436518 - assembly GRCh37
References: dbVar: nsv2775039
dbVar: nssv13644274
dbVar: nssv13640398

Condition

PhenotypeInstruction: See cases