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Items: 1 to 20 of 278

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940691copy number variation1nstd209human GRCh38 chr19: 1,496,051-1,496,118 , GRCh37.p13 chr19: 1,496,050-1,496,117 REEP6
    nsv5673304copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,496,264-1,496,472 , GRCh38.p12 chr19: 1,496,265-1,496,473 REEP6
    nsv5673303copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,486,852-1,491,383 , GRCh38.p12 chr19: 1,486,853-1,491,384 PCSK4, REEP6
    nsv5291342copy number variation1nstd204human GRCh38.p13 chr19: 879,901-2,550,600 , GRCh37.p13 chr19: 879,901-2,550,598 LOC105372240, ELOCP28, 92 more genes
    nsv5284613copy number variation1nstd204human GRCh38.p13 chr19: 1,402,101-1,628,800 , GRCh37.p13 chr19: 1,402,100-1,628,799 TCF3, RN7SL477P, 13 more genes
    nsv5283415copy number variation1nstd204human GRCh37.p13 chr19: 1,478,200-1,534,699 , GRCh38.p13 chr19: 1,478,201-1,534,700 PCSK4, REEP6, 4 more genes
    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
    nsv4623195copy number variation1nstd183human GRCh37 chr19: 1,468,438-1,512,978 , GRCh38.p12 chr19: 1,468,439-1,512,979 ADAMTSL5, APC2, 3 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
    nsv4457632copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,342,624-1,817,866 , GRCh38.p12 chr19: 1,342,625-1,817,867 ONECUT3, UQCR11, 23 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
    nsv4415618copy number variation1nstd174human GRCh37 chr19: 1,486,558-1,516,997 , GRCh38.p12 chr19: 1,486,559-1,516,998 REEP6, LOC107985337, 2 more genes
    nsv4252948copy number variation1nstd166human GRCh37.p13 chr19: 1,498,412-1,498,471 , GRCh38.p12 chr19: 1,498,413-1,498,472 REEP6
    nsv3955463insertion1nstd168human GRCh38 chr19: 1,449,533-1,554,193 , GRCh37.p13 chr19: 1,449,532-1,554,192 APC2, PCSK4, 6 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
    nsv3922550copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-1,952,650 , GRCh37 chr19: 259,395-1,952,649 , NCBI36 chr19: 210,395-1,903,649 LOC102723811, DAZAP1, 99 more genes
    nsv3922151copy number variation1nstd102humanPathogenic NCBI36 chr19: 896,098-1,923,298 , GRCh38 chr19: 945,098-1,972,299 , GRCh37 chr19: 945,098-1,972,298 MIR1909, SBNO2, 58 more genes
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