diff --git a/preClinVar/demo/Variant_sv_range_coords.csv b/preClinVar/demo/Variant_sv_range_coords.csv
index 87fbcc1..8bf5bf7 100644
--- a/preClinVar/demo/Variant_sv_range_coords.csv
+++ b/preClinVar/demo/Variant_sv_range_coords.csv
@@ -1,2 +1,2 @@
 "##Local ID","Linking ID","Chromosome","Reference allele","Alternate allele","Variant type","Copy number","Reference copy number","Outer start","Inner start","Inner stop","Outer stop","Condition ID type","Condition ID value","Clinical significance","Date last evaluated","Mode of inheritance"
-"77d69d4d78a8e272365bdabe4f607327","77d69d4d78a8e272365bdabe4f607327","15","TAAGAATGTTGTGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCCGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGCGTAGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCCCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAA","T","Deletion","1","2","66633800","66633900","66634100","66634200","HPO","HP:0001298;HP:0001250","Likely pathogenic","2022-12-07","Somatic mutation"
+"77d69d4d78a8e272365bdabe4f607327","77d69d4d78a8e272365bdabe4f607327","15","TAAGAATGTTGTGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCCGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGCGTAGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCCCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAA","T","Deletion","1","2","66633800","66633900","66634100","66634200","HPO","HP:0001298;HP:0001250","Likely pathogenic","2022-12-07","Unknown mechanism"