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GRCh38/hg38 2p25.3(chr2:17019-283213)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000143069

Variant: GRCh38/hg38 2p25.3(chr2:17019-283213)x3

Type: Variant
Allele: GRCh38/hg38 2p25.3(chr2:17019-283213)x3 164756
Gene:
Type: copy number gain
Location: Chr2: 17019 - 283213 - assembly GRCh38
Chr2: 17019 - 283213 - assembly GRCh37
Chr2: 7019 - 273213 - assembly NCBI36
Chr2: 17019 - 283213 - assembly GRCh38
References: dbVar: nsv917307
dbVar: nssv1604673

Condition

PhenotypeInstruction: See cases