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GRCh38/hg38 8p21.2(chr8:23757449-24517207)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000136617

Variant: GRCh38/hg38 8p21.2(chr8:23757449-24517207)x3

Type: Variant
Allele: GRCh38/hg38 8p21.2(chr8:23757449-24517207)x3 157177
Gene:
Type: copy number gain
Location: Chr8: 23670907 - 24430610 - assembly NCBI36
Chr8: 23757449 - 24517207 - assembly GRCh38
Chr8: 23614962 - 24374720 - assembly GRCh37
Chr8: 23757449 - 24517207 - assembly GRCh38
References: dbVar: nsv533937
dbVar: nssv582522

Condition

PhenotypeInstruction: See cases