GENETIC ENCYCLOPEDIA
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GRCh37/hg19 Xp22.2(chrX:9787331-9946656)x2 AND not provided

Significance: Likely benign
ClinVar: RCV000753374

Variant: GRCh37/hg19 Xp22.2(chrX:9787331-9946656)x2

Type: Variant
Allele: GRCh37/hg19 Xp22.2(chrX:9787331-9946656)x2 608074
Gene:
Type: copy number gain
Location: ChrX: 9787331 - 9946656 - assembly GRCh37

Condition

Disease: not provided