Disease associated variation - ClinVar Allele ID Type Name RS#dbSNP Phenotype IDs Chromosome Start Stop Reference Alternate 161221 copy number loss GRCh38/hg38 19q13.2(chr19:39010191-39035118)x1 -1 - 19 39500831 39525758 na na 161221 copy number loss GRCh38/hg38 19q13.2(chr19:39010191-39035118)x1 -1 - 19 39010191 39035118 na na 161221 copy number loss GRCh38/hg38 19q13.2(chr19:39010191-39035118)x1 -1 - 19 44192671 44217598 na na