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GRCh37/hg19 10q22.3-23.2(chr10:81630468-88975551)x1 AND See cases

Significance: Pathogenic
ClinVar: RCV000447214

Variant: GRCh37/hg19 10q22.3-23.2(chr10:81630468-88975551)x1

Type: Variant
Allele: GRCh37/hg19 10q22.3-23.2(chr10:81630468-88975551)x1 383194
Gene:
Type: copy number loss
Location: Chr10: 81630468 - 88975551 - assembly GRCh37
References: dbVar: nsv2771966
dbVar: nssv13654231

Condition

PhenotypeInstruction: See cases