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GRCh37/hg19 Yq11.222(chrY:21053353-21251249)x2 AND See cases

Significance: Likely benign
ClinVar: RCV000446583

Variant: GRCh37/hg19 Yq11.222(chrY:21053353-21251249)x2

Type: Variant
Allele: GRCh37/hg19 Yq11.222(chrY:21053353-21251249)x2 381513
Gene:
Type: copy number gain
Location: ChrY: 21053353 - 21251249 - assembly GRCh37
References: dbVar: nsv2773391
dbVar: nssv13654990

Condition

PhenotypeInstruction: See cases