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GRCh37/hg19 4q34.3(chr4:178104930-178478364)x3 AND See cases

Significance: Likely benign
ClinVar: RCV000446603

Variant: GRCh37/hg19 4q34.3(chr4:178104930-178478364)x3

Type: Variant
Allele: GRCh37/hg19 4q34.3(chr4:178104930-178478364)x3 381324
Gene:
Type: copy number gain
Location: Chr4: 178104930 - 178478364 - assembly GRCh37
References: dbVar: nsv2772315
dbVar: nssv13656479

Condition

PhenotypeInstruction: See cases