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GRCh37/hg19 Xp11.3-11.23(chrX:46366112-46407858)x2 AND See cases

Significance: Uncertain significance
ClinVar: RCV000447226

Variant: GRCh37/hg19 Xp11.3-11.23(chrX:46366112-46407858)x2

Type: Variant
Allele: GRCh37/hg19 Xp11.3-11.23(chrX:46366112-46407858)x2 382052
Gene:
Type: copy number gain
Location: ChrX: 46366112 - 46407858 - assembly GRCh37
References: dbVar: nsv2776335
dbVar: nssv13643045

Condition

PhenotypeInstruction: See cases