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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5289021copy number variation1nstd204human GRCh38.p13 chr19: 36,002,801-36,145,200 , GRCh37.p13 chr19: 36,493,703-36,636,102 LOC101927572, THAP8, 10 more genes
    nsv5024579copy number variation1nstd200human GRCh38 chr19: 36,005,869-36,025,618 , GRCh37.p13 chr19: 36,496,771-36,516,520 LOC101927572, ALKBH6, 2 more genes
    nsv5024572copy number variation1nstd200human GRCh38 chr19: 35,818,267-36,019,433 , GRCh37.p13 chr19: 36,309,169-36,510,335 SYNE4, LOC107985317, 13 more genes
    nsv5024570copy number variation1nstd200human GRCh38 chr19: 35,722,805-36,225,611 , GRCh37.p13 chr19: 36,213,707-36,716,513 LOC105372385, ALKBH6, 34 more genes
    nsv4865133copy number variation1nstd200human GRCh37 chr19: 36,213,707-36,716,513 , GRCh38.p12 chr19: 35,722,805-36,225,611 KMT2B, PSENEN, 34 more genes
    nsv4625448copy number variation1nstd183human GRCh37 chr19: 36,505,480-36,505,524 , GRCh38.p12 chr19: 36,014,578-36,014,622 CLIP3, ALKBH6, 1 more genes
    nsv4536962copy number variation1nstd166human GRCh37.p13 chr19: 36,309,999-36,510,300 , GRCh38.p12 chr19: 35,819,097-36,019,398 KIRREL2, HCST, 13 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4349605copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,111,811-37,744,992 , GRCh38.p12 chr19: 34,620,906-37,254,090 ATP4A, RNY5P10, 129 more genes
    nsv4269221copy number variation1nstd166human GRCh37.p13 chr19: 36,496,850-36,516,478 , GRCh38.p12 chr19: 36,005,948-36,025,576 ALKBH6, LOC101927572, 2 more genes
    nsv4257278copy number variation1nstd166human GRCh37.p13 chr19: 36,502,747-36,509,240 , GRCh38.p12 chr19: 36,011,845-36,018,338 LOC101927572, ALKBH6, 1 more genes
    nsv4252845copy number variation1nstd166human GRCh37.p13 chr19: 36,499,000-36,504,000 , GRCh38.p12 chr19: 36,008,098-36,013,098 CLIP3, SYNE4, 2 more genes
    nsv3919296copy number variation1nstd102humanPathogenic NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723 UBA2, ZNF529, 241 more genes
    nsv3916007copy number variation1nstd102humanPathogenic GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990 MAG, RNU6-967P, 238 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3909857copy number variation1nstd102humanUncertain significance GRCh37 chr19: 36,475,577-38,399,402 , GRCh38.p12 chr19: 35,984,675-37,908,762 ZNF790, ZNF571-AS1, 72 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3902356copy number variation1nstd102humanUncertain significance GRCh37 chr19: 36,147,111-37,249,653 , GRCh38.p12 chr19: 35,656,209-36,758,751 RNY5P10, ZNF146, 56 more genes
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