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GRCh37/hg19 Yq11.21(chrY:13992304-14389646)x2 AND See cases

Significance: Benign
ClinVar: RCV000446564

Variant: GRCh37/hg19 Yq11.21(chrY:13992304-14389646)x2

Type: Variant
Allele: GRCh37/hg19 Yq11.21(chrY:13992304-14389646)x2 381244
Gene:
Type: copy number gain
Location: ChrY: 13992304 - 14389646 - assembly GRCh37
References: dbVar: nsv2771946
dbVar: nssv13648826

Condition

PhenotypeInstruction: See cases