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GRCh37/hg19 7q36.3(chr7:158424788-158668137)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000447195

Variant: GRCh37/hg19 7q36.3(chr7:158424788-158668137)x3

Type: Variant
Allele: GRCh37/hg19 7q36.3(chr7:158424788-158668137)x3 382026
Gene:
Type: copy number gain
Location: Chr7: 158424788 - 158668137 - assembly GRCh37
References: dbVar: nsv2776182
dbVar: nssv13643169

Condition

PhenotypeInstruction: See cases