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Items: 1 to 20 of 282

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5515810copy number variation1nstd206human GRCh38 chr19: 1,911,123-1,911,460 , GRCh37.p13 chr19: 1,911,122-1,911,459 SCAMP4, ADAT3
    nsv5380252translocation1nstd200human GRCh38 chr19: 1,910,727-1,910,727 , GRCh38 chr19: 1,903,786-1,903,786 , GRCh37.p13 chr19: 1,910,726-1,910,726 , GRCh37.p13 chr19: 1,903,785-1,903,785 SCAMP4, ADAT3
    nsv5294229copy number variation1nstd204human GRCh38.p13 chr19: 1,717,401-2,347,800 , GRCh37.p13 chr19: 1,717,400-2,347,798 DOT1L, LOC107985278, 32 more genes
    nsv5291342copy number variation1nstd204human GRCh38.p13 chr19: 879,901-2,550,600 , GRCh37.p13 chr19: 879,901-2,550,598 LOC105372240, ELOCP28, 92 more genes
    nsv5029216copy number variation1nstd200human GRCh38 chr19: 1,801,870-1,929,932 , GRCh37.p13 chr19: 1,801,869-1,929,931 ABHD17A, SCAMP4, 6 more genes
    nsv5019099copy number variation1nstd200human GRCh38 chr19: 1,903,011-1,904,045 , GRCh37.p13 chr19: 1,903,010-1,904,044 ADAT3, SCAMP4
    nsv4676366copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 1,075,192-2,256,387 , GRCh38.p12 chr19: 1,075,193-2,256,388 AMH, ATP5F1D, 64 more genes
    nsv4676346copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,501,271 , GRCh38.p12 chr19: 260,911-3,501,273 AZU1, REEP6, 159 more genes
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 MRPL54, DAZAP1, 198 more genes
    nsv4626791copy number variation1nstd183human GRCh37 chr19: 1,907,479-1,922,939 , GRCh38.p12 chr19: 1,907,480-1,922,940 SCAMP4, ADAT3
    nsv4457801copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,816,218-2,152,190 , GRCh38.p12 chr19: 1,816,219-2,152,191 AP3D1, CSNK1G2, 14 more genes
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 BSG, LOC100420586, 217 more genes
    nsv4457717copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,772,993-1,990,715 , GRCh38.p12 chr19: 1,772,994-1,990,716 KLF16, SCAMP4, 12 more genes
    nsv4452268copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,406,030-3,597,207 , GRCh38.p12 chr19: 1,406,031-3,597,209 C19orf25, MIR7108, 92 more genes
    nsv4272156copy number variation1nstd166human GRCh37.p13 chr19: 1,903,786-1,910,726 , GRCh38.p12 chr19: 1,903,787-1,910,727 ADAT3, SCAMP4
    nsv4271913copy number variation1nstd166human GRCh37.p13 chr19: 1,902,461-1,905,823 , GRCh38.p12 chr19: 1,902,462-1,905,824 ADAT3, SCAMP4
    nsv4267110copy number variation1nstd166human GRCh37.p13 chr19: 1,764,730-2,071,821 , GRCh38.p12 chr19: 1,764,731-2,071,822 LOC100288123, LOC101928543, 15 more genes
    nsv4264886copy number variation1nstd166human GRCh37.p13 chr19: 1,881,790-1,933,403 , GRCh38.p12 chr19: 1,881,791-1,933,404 SCAMP4, ABHD17A, 1 more genes
    nsv3924102copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622 POLR2E, PWWP3A, 283 more genes
    nsv3923561copy number variation1nstd102humanPathogenic NCBI36 chr19: 184,565-4,650,484 , GRCh37 chr19: 233,565-4,699,484 , GRCh38 chr19: 233,565-4,699,472 DAPK3, IZUMO4, 214 more genes
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