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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    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
    nsv7006717copy number variation1nstd229human GRCh38 chr19: 40,448,493-40,452,768 , GRCh37.p13 chr19: 40,954,400-40,958,675 BLVRB
    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
    nsv7006013copy number variation1nstd229human GRCh38 chr19: 40,450,925-40,450,955 , GRCh37.p13 chr19: 40,956,832-40,956,862 BLVRB
    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
    nsv7003885copy number variation1nstd229human GRCh38 chr19: 40,454,110-40,457,982 , GRCh37.p13 chr19: 40,960,017-40,963,889 BLVRB
    nsv7002699copy number variation1nstd229human GRCh38 chr19: 40,450,665-40,464,316 , GRCh37.p13 chr19: 40,956,572-40,970,223 BLVRB
    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
    nsv7001151copy number variation1nstd229human GRCh38 chr19: 40,446,601-40,457,400 , GRCh37.p13 chr19: 40,952,508-40,963,307 BLVRB
    nsv6998559copy number variation1nstd229human GRCh38 chr19: 40,461,558-40,523,096 , GRCh37.p13 chr19: 40,967,465-41,029,003 BLVRB, SPTBN4
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6533593copy number variation1nstd223human GRCh38 chr19: 40,451,239-40,462,564 , GRCh37.p13 chr19: 40,957,146-40,968,471 BLVRB
    nsv6531495copy number variation1nstd223human GRCh38 chr19: 40,448,508-40,452,738 , GRCh37.p13 chr19: 40,954,415-40,958,645 BLVRB
    nsv6526067copy number variation1nstd223human GRCh38 chr19: 40,462,259-40,465,021 , GRCh37.p13 chr19: 40,968,166-40,970,928 SPTBN4, BLVRB
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