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GRCh38/hg38 8p21.2(chr8:24463803-25049184)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000052168

Variant: GRCh38/hg38 8p21.2(chr8:24463803-25049184)x3

Type: Variant
Allele: GRCh38/hg38 8p21.2(chr8:24463803-25049184)x3 73009
Gene:
Type: copy number gain
Location: Chr8: 24377206 - 24962616 - assembly NCBI36
Chr8: 24463803 - 25049184 - assembly GRCh38
Chr8: 24321316 - 24906699 - assembly GRCh37
Chr8: 24463803 - 25049184 - assembly GRCh38
References: dbVar: nsv530879
dbVar: nssv581324

Condition

PhenotypeInstruction: See cases