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GRCh37/hg19 18q22.1(chr18:65687087-66530088)x4 AND See cases

Significance: Uncertain significance
ClinVar: RCV000447252

Variant: GRCh37/hg19 18q22.1(chr18:65687087-66530088)x4

Type: Variant
Allele: GRCh37/hg19 18q22.1(chr18:65687087-66530088)x4 382713
Gene:
Type: copy number gain
Location: Chr18: 65687087 - 66530088 - assembly GRCh37
References: dbVar: nsv2768838
dbVar: nssv13655437
dbVar: nssv13641263

Condition

PhenotypeInstruction: See cases