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GRCh37/hg19 11p15.5-15.3(chr11:193146-12643136) AND Russell-Silver syndrome

Significance: Pathogenic
ClinVar: RCV000767567

Variant: GRCh37/hg19 11p15.5-15.3(chr11:193146-12643136)

Type: Variant
Allele: GRCh37/hg19 11p15.5-15.3(chr11:193146-12643136) 613863
Gene:
Type: copy number gain
Location: Chr11: 193146 - 12643136 - assembly GRCh37

Condition

Disease: Russell-Silver syndrome