GENETIC ENCYCLOPEDIA
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GRCh37/hg19 2p25.3(chr2:192760-659746)x3 AND not provided

Significance: Likely benign
ClinVar: RCV000682077

Variant: GRCh37/hg19 2p25.3(chr2:192760-659746)x3

Type: Variant
Allele: GRCh37/hg19 2p25.3(chr2:192760-659746)x3 553772
Gene:
Type: copy number gain
Location: Chr2: 192760 - 659746 - assembly GRCh37

Condition

Disease: not provided