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GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3 AND See cases

Significance: Pathogenic
ClinVar: RCV000447207

Variant: GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3

Type: Variant
Allele: GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3 384362
Gene:
Type: copy number gain
Location: Chr9: 203861 - 141020389 - assembly GRCh37
References: dbVar: nsv995513
dbVar: nssv13646368
dbVar: nssv13640208

Condition

PhenotypeInstruction: See cases