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GRCh37/hg19 3p26.3(chr3:282750-1287912)x1 AND See cases

Significance: Uncertain significance
ClinVar: RCV000446557

Variant: GRCh37/hg19 3p26.3(chr3:282750-1287912)x1

Type: Variant
Allele: GRCh37/hg19 3p26.3(chr3:282750-1287912)x1 383113
Gene:
Type: copy number loss
Location: Chr3: 282750 - 1287912 - assembly GRCh37
References: dbVar: nsv2771402
dbVar: nssv13649402

Condition

PhenotypeInstruction: See cases