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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142129copy number variation1nstd232human GRCh37.p13 chr19: 41,000,421-41,000,491 , GRCh38.p12 chr19: 40,494,514-40,494,584 SPTBN4
    nsv7095480copy number variation4nstd102humanUncertain significance GRCh37 chr19: 39,904,727-42,931,301 , GRCh38.p12 chr19: 39,414,087-42,427,149 CYP2B6, EID2B, 140 more genes
    nsv7095278copy number variation1nstd102humanUncertain significance GRCh37 chr19: 40,882,496-41,135,455 , GRCh38.p12 chr19: 40,376,589-40,629,550 HIPK4, PRX, 8 more genes
    nsv7071361inversion1nstd229human GRCh38 chr19: 39,004,066-42,402,005 , GRCh37.p13 chr19: 39,494,706-42,906,157 RAB4B, RABAC1, 160 more genes
    nsv7068818inversion1nstd229human GRCh38 chr19: 40,559,823-40,559,903 , GRCh37.p13 chr19: 41,065,729-41,065,809 SPTBN4
    nsv7068288inversion1nstd229human GRCh38 chr19: 39,023,970-42,945,419 , GRCh37.p13 chr19: 39,514,610-43,449,571 MIR4530, RNU6-195P, 178 more genes
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 more genes
    nsv7018080copy number variation1nstd229human GRCh38 chr19: 40,537,731-40,537,779 , GRCh37.p13 chr19: 41,043,637-41,043,685 SPTBN4
    nsv7012799copy number variation1nstd229human GRCh38 chr19: 40,481,766-40,485,161 , GRCh37.p13 chr19: 40,987,673-40,991,068 SPTBN4
    nsv7012661copy number variation1nstd229human GRCh38 chr19: 40,541,159-40,548,007 , GRCh37.p13 chr19: 41,047,065-41,053,913 SPTBN4
    nsv7008574copy number variation1nstd229human GRCh38 chr19: 40,534,253-40,534,447 , GRCh37.p13 chr19: 41,040,160-41,040,354 SPTBN4
    nsv7008184copy number variation1nstd229human GRCh38 chr19: 40,473,301-40,478,800 , GRCh37.p13 chr19: 40,979,208-40,984,707 SPTBN4
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7006684copy number variation1nstd229human GRCh38 chr19: 40,438,655-40,552,046 , GRCh37.p13 chr19: 40,944,562-41,057,952 BLVRB, SERTAD3-AS1, 2 more genes
    nsv7005657copy number variation1nstd229human GRCh38 chr19: 40,541,952-40,580,031 , GRCh37.p13 chr19: 41,047,858-41,085,937 SHKBP1, SPTBN4
    nsv7004420copy number variation1nstd229human GRCh38 chr19: 40,416,802-40,503,506 , GRCh37.p13 chr19: 40,922,709-41,009,413 BLVRB, SERTAD3, 3 more genes
    nsv7004380copy number variation1nstd229human GRCh38 chr19: 40,462,259-40,465,023 , GRCh37.p13 chr19: 40,968,166-40,970,930 SPTBN4, BLVRB
    nsv7003773copy number variation1nstd229human GRCh38 chr19: 40,503,243-40,503,432 , GRCh37.p13 chr19: 41,009,150-41,009,339 SPTBN4
    nsv7002183copy number variation1nstd229human GRCh38 chr19: 40,225,202-40,756,025 , GRCh37.p13 chr19: 40,731,109-41,261,930 RNU6-195P, LTBP4, 21 more genes
    nsv6999903copy number variation1nstd229human GRCh38 chr19: 40,473,329-40,478,827 , GRCh37.p13 chr19: 40,979,236-40,984,734 SPTBN4
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