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GRCh37/hg19 Xp22.33(chrX:1321581-1570890)x3 AND See cases

Significance: Benign
ClinVar: RCV000446634

Variant: GRCh37/hg19 Xp22.33(chrX:1321581-1570890)x3

Type: Variant
Allele: GRCh37/hg19 Xp22.33(chrX:1321581-1570890)x3 381625
Gene:
Type: copy number gain
Location: ChrX: 1321581 - 1570890 - assembly GRCh37
References: dbVar: nsv2773975
dbVar: nssv13649351

Condition

PhenotypeInstruction: See cases