GENETIC ENCYCLOPEDIA
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GRCh37/hg19 17q12(chr17:34849849-36151287)x3 AND See cases

Significance: Pathogenic
ClinVar: RCV000446641

Variant: GRCh37/hg19 17q12(chr17:34849849-36151287)x3

Type: Variant
Allele: GRCh37/hg19 17q12(chr17:34849849-36151287)x3 381917
Gene:
Type: copy number gain
Location: Chr17: 34849849 - 36151287 - assembly GRCh37
References: dbVar: nsv2775541
dbVar: nssv13655994

Condition

PhenotypeInstruction: See cases