| Disease associated variation - ClinVar | | Allele ID | Type | Name | RS#dbSNP | Phenotype IDs | Chromosome | Start | Stop | Reference | Alternate |
|---|
| 156400 | copy number loss | GRCh38/hg38 5q12.3(chr5:64344867-64370545)x1 | -1 | - | 5 | 63640694 | 63666372 | na | na | | 156400 | copy number loss | GRCh38/hg38 5q12.3(chr5:64344867-64370545)x1 | -1 | - | 5 | 64344867 | 64370545 | na | na | | 156400 | copy number loss | GRCh38/hg38 5q12.3(chr5:64344867-64370545)x1 | -1 | - | 5 | 63676450 | 63702128 | na | na | |