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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6312151copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr6: 3,157,621-3,157,697 , GRCh38.p12 chr6: 3,157,387-3,157,463 LOC105374889, TUBB2A
    nsv997095copy number variation1nstd45humanPathogenic GRCh37 chrX: 15,843,929-15,873,137 , GRCh38.p12 chrX: 15,825,806-15,855,014 ZRSR2, AP1S2
    nsv6312475copy number variation1nstd102humanUncertain significance GRCh37 chr6: 3,155,839-3,157,697 , GRCh38.p12 chr6: 3,155,605-3,157,463 TUBB2A, LOC105374889
    nsv3882115copy number variation1nstd102humanBenign GRCh37 chr6: 3,144,120-3,155,947 , GRCh38.p12 chr6: 3,143,886-3,155,713 LOC105374889, BPHL, 1 more genes
    nsv4455280copy number variation1nstd102humanUncertain significance GRCh37 chr6: 3,151,303-3,220,269 , GRCh38.p12 chr6: 3,151,069-3,220,035 BPHL, TUBB2BP1, 3 more genes
    nsv7097328copy number variation1nstd102humanUncertain significance GRCh37 chr6: 3,155,839-3,226,065 , GRCh38.p12 chr6: 3,155,605-3,225,831 TUBB2A, TUBB2BP1, 3 more genes
    nsv4457099copy number variation1nstd102humanUncertain significance GRCh37 chr6: 3,157,235-3,218,178 , GRCh38.p12 chr6: 3,157,001-3,217,944 TUBB2A, LINC02525, 2 more genes
    nsv7097820copy number variation1nstd102humanUncertain significance GRCh37 chr6: 3,104,439-3,157,697 , GRCh38.p12 chr6: 3,104,205-3,157,463 TUBB2A, RIPK1, 3 more genes
    nsv7095430copy number variation1nstd102humanUncertain significance GRCh37 chr18: 12,329,564-12,377,081 , GRCh38.p12 chr18: 12,329,565-12,377,082 TUBB6, LOC107985154, 1 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv3916217copy number variation1nstd102humanPathogenic NCBI36 chr18: 4,275-16,783,904 , GRCh37.p13 chr18: 14,275-18,529,906 , GRCh38.p12 chr18: 14,275-20,949,945 LOC101927410, APCDD1, 276 more genes
    nsv4676141copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-18,529,578 , GRCh38.p12 chr18: 136,226-20,949,617 ANKRD12, DLGAP1-AS1, 270 more genes
    nsv6290328copy number variation1nstd102humanPathogenic GRCh37 chr18: 10,501-15,410,398 , GRCh38.p12 chr18: 10,501-15,410,399 RNA5SP449, MPPE1, 275 more genes
    nsv7098917copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-15,400,035 , GRCh38.p12 chr18: 10,001-15,400,036 RNU7-25P, RPL6P27, 275 more genes
    nsv3905455copy number variation1nstd102humanPathogenic GRCh37 chr18: 13,034-15,375,878 , GRCh38.p12 chr18: 13,034-15,375,879 LOC100533852, LINC01906, 275 more genes
    nsv4676393copy number variation1nstd102humanPathogenic GRCh37 chr18: 13,034-15,330,525 , GRCh38.p12 chr18: 13,034-15,330,526 PRELID3A, ANKRD30B, 275 more genes
    nsv3898793copy number variation1nstd102humanPathogenic GRCh37 chr18: 14,316-15,328,499 , GRCh38.p12 chr18: 14,316-15,328,500 LOC100419892, LOC107985173, 275 more genes
    nsv3907765copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-15,157,836 , GRCh38.p12 chr18: 10,001-15,157,837 LOC105372003, YES1, 269 more genes
    nsv3896525copy number variation5nstd102humanPathogenic GRCh37 chr18: 136,226-15,198,990 , GRCh38.p12 chr18: 136,226-15,198,991 PRELID3A, LOC646203, 264 more genes
    nsv3897591copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-15,198,989 , GRCh38.p12 chr18: 136,226-15,198,990 LOC107985155, LOC646203, 264 more genes
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