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GRCh38/hg38 8p21.2(chr8:23961808-25436108)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000052167

Variant: GRCh38/hg38 8p21.2(chr8:23961808-25436108)x3

Type: Variant
Allele: GRCh38/hg38 8p21.2(chr8:23961808-25436108)x3 73008
Gene:
Type: copy number gain
Location: Chr8: 23875266 - 25349541 - assembly NCBI36
Chr8: 23961808 - 25436108 - assembly GRCh38
Chr8: 23819321 - 25293624 - assembly GRCh37
Chr8: 23961808 - 25436108 - assembly GRCh38
References: dbVar: nsv530878
dbVar: nssv581323

Condition

PhenotypeInstruction: See cases