Disease associated variation - ClinVar Allele ID Type Name RS#dbSNP Phenotype IDs Chromosome Start Stop Reference Alternate 71759 copy number gain GRCh38/hg38 6q21(chr6:112309208-113197212)x3 -1 - 6 112630410 113518414 na na 71759 copy number gain GRCh38/hg38 6q21(chr6:112309208-113197212)x3 -1 - 6 112309208 113197212 na na 71759 copy number gain GRCh38/hg38 6q21(chr6:112309208-113197212)x3 -1 - 6 112737103 113625107 na na