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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5723538mobile element insertion1nstd211human GRCh38 chr19: 35,762,729-35,762,729 , GRCh37.p13 chr19: 36,253,630-36,253,630 PROSER3
    nsv5027710copy number variation1nstd200human GRCh38 chr19: 35,768,285-35,771,821 , GRCh37.p13 chr19: 36,259,187-36,262,723 PROSER3
    nsv5027709copy number variation1nstd200human GRCh38 chr19: 35,764,530-35,765,644 , GRCh37.p13 chr19: 36,255,431-36,256,545 PROSER3
    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
    nsv4861323copy number variation1nstd200human GRCh37 chr19: 36,255,431-36,256,545 , GRCh38.p12 chr19: 35,764,530-35,765,644 PROSER3
    nsv4674329copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,553,425-36,264,299 , GRCh38.p12 chr19: 35,062,521-35,773,397 LOC105372379, LSR, 50 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
    nsv4350190copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,043,556-36,316,644 , GRCh38.p12 chr19: 34,552,651-35,825,742 SCN1B, ETV2, 76 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
    nsv4261902copy number variation1nstd166human GRCh37.p13 chr19: 36,259,187-36,262,723 , GRCh38.p12 chr19: 35,768,285-35,771,821 PROSER3
    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
    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
    nsv3168446copy number variation1nstd158human GRCh37 chr19: 35,445,908-45,506,757 , GRCh38.p12 chr19: 34,955,004-45,003,499 , ACTN4, 449 more genes
    nsv3166676copy number variation1nstd151human GRCh37 chr19: 36,234,910-36,259,450 , GRCh38.p12 chr19: 35,744,009-35,768,548 U2AF1L4, LIN37, 3 more genes
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