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GRCh38/hg38 6q13-24.1(chr6:74382807-142040500)x3 AND See cases

Significance: Pathogenic
ClinVar: RCV000139729

Variant: GRCh38/hg38 6q13-24.1(chr6:74382807-142040500)x3

Type: Variant
Allele: GRCh38/hg38 6q13-24.1(chr6:74382807-142040500)x3 160688
Gene:
Type: copy number gain
Location: Chr6: 74382807 - 142040500 - assembly GRCh38
Chr6: 75092523 - 142361637 - assembly GRCh37
Chr6: 75149243 - 142403330 - assembly NCBI36
Chr6: 74382807 - 142040500 - assembly GRCh38
References: dbVar: nsv917239
dbVar: nssv1604903

Condition

PhenotypeInstruction: See cases