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GRCh37/hg19 Xq28(chrX:152157384-152226248)x3 AND See cases

Significance: Likely benign
ClinVar: RCV000447283

Variant: GRCh37/hg19 Xq28(chrX:152157384-152226248)x3

Type: Variant
Allele: GRCh37/hg19 Xq28(chrX:152157384-152226248)x3 381067
Gene:
Type: copy number gain
Location: ChrX: 152157384 - 152226248 - assembly GRCh37
References: dbVar: nsv2770989
dbVar: nssv13653457

Condition

PhenotypeInstruction: See cases