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GRCh37/hg19 18p11.32(chr18:811169-2118889)x1 AND See cases

Significance: Likely benign
ClinVar: RCV000447219

Variant: GRCh37/hg19 18p11.32(chr18:811169-2118889)x1

Type: Variant
Allele: GRCh37/hg19 18p11.32(chr18:811169-2118889)x1 383211
Gene:
Type: copy number loss
Location: Chr18: 811169 - 2118889 - assembly GRCh37
References: dbVar: nsv2772071
dbVar: nssv13646436

Condition

PhenotypeInstruction: See cases