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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935756copy number variation1nstd209human GRCh38 chr19: 1,600,495-1,608,281 , GRCh37.p13 chr19: 1,600,494-1,608,280 UQCR11, TCF3
    nsv5874472copy number variation1nstd209human GRCh38 chr19: 1,600,600-1,608,287 , GRCh37.p13 chr19: 1,600,599-1,608,286 TCF3, UQCR11
    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
    nsv5281649copy number variation1nstd204human GRCh38.p13 chr19: 1,600,350-1,607,587 , GRCh37.p13 chr19: 1,600,349-1,607,586 TCF3, UQCR11
    nsv5019068copy number variation1nstd200human GRCh38 chr19: 1,605,163-1,605,816 , GRCh37.p13 chr19: 1,605,162-1,605,815 UQCR11
    nsv5019067copy number variation1nstd200human GRCh38 chr19: 1,604,038-1,606,606 , GRCh37.p13 chr19: 1,604,037-1,606,605 UQCR11
    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
    nsv4628288copy number variation1nstd183human GRCh37 chr19: 1,605,389-1,611,202 , GRCh38.p12 chr19: 1,605,390-1,611,203 UQCR11, TCF3
    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
    nsv4267109copy number variation1nstd166human GRCh37.p13 chr19: 1,600,000-1,605,000 , GRCh38.p12 chr19: 1,600,001-1,605,001 UQCR11
    nsv3969571insertion1nstd168human GRCh38 chr19: 1,575,392-1,635,386 , GRCh37.p13 chr19: 1,575,391-1,635,385 TCF3, UQCR11, 2 more genes
    nsv3964474copy number variation1nstd168human GRCh38 chr19: 1,588,257-1,635,386 , GRCh37.p13 chr19: 1,588,256-1,635,385 MBD3, UQCR11, 2 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
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