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GRCh37/hg19 6q13-14.1(chr6:75889207-76522602)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000448854

Variant: GRCh37/hg19 6q13-14.1(chr6:75889207-76522602)x3

Type: Variant
Allele: GRCh37/hg19 6q13-14.1(chr6:75889207-76522602)x3 383948
Gene:
Type: copy number gain
Location: Chr6: 75889207 - 76522602 - assembly GRCh37
References: dbVar: nsv2776694
dbVar: nssv13643350

Condition

PhenotypeInstruction: See cases