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GRCh37/hg19 15q21.3-22.2(chr15:54713558-62769295)x1 AND See cases

Significance: Pathogenic
ClinVar: RCV000446622

Variant: GRCh37/hg19 15q21.3-22.2(chr15:54713558-62769295)x1

Type: Variant
Allele: GRCh37/hg19 15q21.3-22.2(chr15:54713558-62769295)x1 382086
Gene:
Type: copy number loss
Location: Chr15: 54713558 - 62769295 - assembly GRCh37
References: dbVar: nsv2776530
dbVar: nssv13646131

Condition

PhenotypeInstruction: See cases