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GRCh37/hg19 6q12(chr6:65564377-65671149)x1 AND See cases

Significance: Uncertain significance
ClinVar: RCV000446627

Variant: GRCh37/hg19 6q12(chr6:65564377-65671149)x1

Type: Variant
Allele: GRCh37/hg19 6q12(chr6:65564377-65671149)x1 382793
Gene:
Type: copy number loss
Location: Chr6: 65564377 - 65671149 - assembly GRCh37
References: dbVar: nsv2769394
dbVar: nssv13656188

Condition

PhenotypeInstruction: See cases