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GRCh38/hg38 8p21.3-21.2(chr8:22946697-25125997)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000137878

Variant: GRCh38/hg38 8p21.3-21.2(chr8:22946697-25125997)x3

Type: Variant
Allele: GRCh38/hg38 8p21.3-21.2(chr8:22946697-25125997)x3 158564
Gene:
Type: copy number gain
Location: Chr8: 22860155 - 25039429 - assembly NCBI36
Chr8: 22946697 - 25125997 - assembly GRCh38
Chr8: 22804210 - 24983512 - assembly GRCh37
Chr8: 22946697 - 25125997 - assembly GRCh38
References: dbVar: nsv869062
dbVar: nssv1495353

Condition

PhenotypeInstruction: See cases