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GRCh37/hg19 20p12.1(chr20:14756520-15199338)x1 AND See cases

Significance: Benign
ClinVar: RCV000446596

Variant: GRCh37/hg19 20p12.1(chr20:14756520-15199338)x1

Type: Variant
Allele: GRCh37/hg19 20p12.1(chr20:14756520-15199338)x1 381888
Gene:
Type: copy number loss
Location: Chr20: 14756520 - 15199338 - assembly GRCh37
References: dbVar: nsv2775400
dbVar: nssv13640957

Condition

PhenotypeInstruction: See cases