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GRCh37/hg19 2p15-11.2(chr2:62245236-86978895)x3 AND See cases

Significance: Pathogenic
ClinVar: RCV000448688

Variant: GRCh37/hg19 2p15-11.2(chr2:62245236-86978895)x3

Type: Variant
Allele: GRCh37/hg19 2p15-11.2(chr2:62245236-86978895)x3 383739
Gene:
Type: copy number gain
Location: Chr2: 62245236 - 86978895 - assembly GRCh37
References: dbVar: nsv2775326
dbVar: nssv13645876

Condition

PhenotypeInstruction: See cases