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GRCh38/hg38 8p21.2(chr8:24017764-24642890)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000142014

Variant: GRCh38/hg38 8p21.2(chr8:24017764-24642890)x3

Type: Variant
Allele: GRCh38/hg38 8p21.2(chr8:24017764-24642890)x3 163478
Gene:
Type: copy number gain
Location: Chr8: 23931222 - 24556293 - assembly NCBI36
Chr8: 24017764 - 24642890 - assembly GRCh38
Chr8: 23875277 - 24500403 - assembly GRCh37
Chr8: 24017764 - 24642890 - assembly GRCh38
References: dbVar: nsv995721
dbVar: nssv3394919

Condition

PhenotypeInstruction: See cases