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GRCh37/hg19 15q21.1-22.2(chr15:48000433-60747551)x3 AND not provided

Significance: Pathogenic
ClinVar: RCV000845891

Variant: GRCh37/hg19 15q21.1-22.2(chr15:48000433-60747551)x3

Type: Variant
Allele: GRCh37/hg19 15q21.1-22.2(chr15:48000433-60747551)x3 672775
Gene:
Type: copy number gain
Location: Chr15: 48000433 - 60747551 - assembly GRCh37

Condition

Disease: not provided