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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6290361copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chr9: 138,660,696-138,660,697 , GRCh38 chr9: 135,768,850-135,768,851 KCNT1
    nsv5674067copy number variation1nstd102humanLikely benign GRCh37 chr9: 138,606,413-138,606,576 , GRCh38.p12 chr9: 135,714,567-135,714,730 KCNT1
    nsv6314736copy number variation1nstd102humanLikely benign GRCh38 chr9: 135,784,903-135,784,959 , GRCh37 chr9: 138,676,749-138,676,805 KCNT1
    nsv7097702copy number variation1nstd102humanUncertain significance GRCh37 chr9: 138,641,924-138,649,247 , GRCh38.p12 chr9: 135,750,078-135,757,401 KCNT1
    nsv6635978copy number variation1nstd102humanUncertain significance GRCh37 chr9: 138,649,895-138,650,028 , GRCh38 chr9: 135,758,049-135,758,182 KCNT1
    nsv3889289copy number variation1nstd102humanUncertain significance GRCh38 chr9: 135,759,650-135,759,879 , GRCh37 chr9: 138,651,496-138,651,725 KCNT1
    nsv7098438copy number variation1nstd102humanUncertain significance GRCh37 chr9: 138,606,403-138,606,586 , GRCh38.p12 chr9: 135,714,557-135,714,740 KCNT1
    nsv3884966copy number variation1nstd102humanUncertain significance GRCh37 chr9: 138,667,136-138,680,028 , GRCh38 chr9: 135,775,290-135,788,182 KCNT1, LOC107987140
    nsv4682026copy number variation1nstd102humanUncertain significance GRCh37 chr9: 138,678,023-138,684,027 , GRCh38.p12 chr9: 135,786,177-135,792,181 KCNT1, LOC107987140
    nsv4683836copy number variation1nstd102humanUncertain significance GRCh37 chr9: 138,661,773-138,684,027 , GRCh38.p12 chr9: 135,769,927-135,792,181 KCNT1, LOC107987140
    nsv6312762copy number variation1nstd102humanUncertain significance GRCh37 chr9: 138,585,443-138,606,586 , GRCh38.p12 chr9: 135,693,597-135,714,740 KCNT1, SOHLH1
    nsv4450120copy number variation1nstd102humanUncertain significance GRCh37 chr9: 138,594,085-138,606,586 , GRCh38 chr9: 135,702,239-135,714,740 KCNT1, SOHLH1
    nsv1398289copy number variation1nstd102humanUncertain significance GRCh38 chr9: 135,665,886-135,775,364 , GRCh37 chr9: 138,557,731-138,667,209 KCNT1, LOC105376317, 3 more genes
    nsv3918779copy number variation1nstd102humanPathogenic GRCh37 chr9: 137,320,520-141,049,374 , NCBI36 chr9: 136,460,341-140,169,195 , GRCh38 chr9: 134,428,674-138,154,922 KCNT1, LRRC26, 160 more genes
    nsv3891854copy number variation1nstd102humanPathogenic GRCh37 chr9: 137,816,459-141,114,095 , GRCh38.p12 chr9: 134,924,613-138,223,645 KCNT1, LCN10, 147 more genes
    nsv3899903copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,209,358-141,020,389 , GRCh38.p12 chr9: 135,317,512-138,125,937 KCNT1, NSMF, 137 more genes
    nsv3896336copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,222,049-141,018,925 , GRCh38.p12 chr9: 135,330,203-138,124,473 KCNT1, LINC02907, 137 more genes
    nsv4685995copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,225,001-141,015,001 , GRCh38.p12 chr9: 135,333,155-138,120,549 KCNT1, TPRN, 137 more genes
    nsv7098070copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 138,392,557-141,016,451 , GRCh38.p12 chr9: 135,500,711-138,121,999 KCNT1, STPG3-AS1, 132 more genes
    nsv7093414copy number variation1nstd102humanPathogenic GRCh38 chr9: 134,932,722-137,269,957 , GRCh37.p13 chr9: 137,824,568-140,164,409 KCNT1, LHX3, 121 more genes
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