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GRCh37/hg19 8p21.2-q12.1(chr8:24772064-24813176)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000446588

Variant: GRCh37/hg19 8p21.2-q12.1(chr8:24772064-24813176)x3

Type: Variant
Allele: GRCh37/hg19 8p21.2-q12.1(chr8:24772064-24813176)x3 380886
Gene:
Type: copy number gain
Location: Chr8: 24772064 - 56509566 - assembly GRCh37
References: dbVar: nsv2770008
dbVar: nssv13642101

Condition

PhenotypeInstruction: See cases