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Items: 1 to 20 of 116

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974443insertion1nstd209human GRCh38 chr19: 49,154,274-49,154,274 , GRCh37.p13 chr19: 49,657,531-49,657,531 HRC
    nsv5938257copy number variation1nstd209human GRCh38 chr19: 49,154,308-49,154,619 , GRCh37.p13 chr19: 49,657,565-49,657,876 HRC
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5655519insertion1nstd207human GRCh38 chr19: 49,154,274-49,154,274 , GRCh37.p13 chr19: 49,657,531-49,657,531 HRC
    nsv5520447copy number variation1nstd206human GRCh38 chr19: 49,131,438-49,174,442 , GRCh37.p13 chr19: 49,634,695-49,677,699 TRPM4, PPFIA3, 1 more genes
    nsv5024801copy number variation1nstd200human GRCh38 chr19: 49,131,438-49,174,442 , GRCh37.p13 chr19: 49,634,695-49,677,699 TRPM4, PPFIA3, 1 more genes
    nsv4865253copy number variation1nstd200human GRCh37 chr19: 49,634,695-49,677,699 , GRCh38.p12 chr19: 49,131,438-49,174,442 HRC, TRPM4, 1 more genes
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4685766copy number variation1nstd102humannot provided GRCh37 chr19: 49,640,430-49,703,884 , GRCh38.p12 chr19: 49,137,173-49,200,627 HRC, TRPM4, 1 more genes
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4621698copy number variation1nstd183human GRCh37 chr19: 49,654,366-49,654,611 , GRCh38.p12 chr19: 49,151,109-49,151,354 HRC, PPFIA3
    nsv4457465copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,600,909-51,366,070 , GRCh38.p12 chr19: 49,097,652-50,862,814 MED25, EMC10, 117 more genes
    nsv4427263copy number variation1nstd174human GRCh37 chr19: 49,618,778-49,686,591 , GRCh38.p12 chr19: 49,115,521-49,183,334 C19orf73, PPFIA3, 3 more genes
    nsv4378981copy number variation1nstd173human GRCh37 chr19: 49,654,265-49,753,571 , GRCh38.p12 chr19: 49,151,008-49,250,314 HRC, TRPM4, 2 more genes
    nsv4376838copy number variation1nstd173human GRCh37 chr19: 48,462,617-51,107,899 , GRCh38.p12 chr19: 47,959,360-50,604,642 , LIN7B, 173 more genes
    nsv4375168copy number variation1nstd173human GRCh37 chr19: 49,572,056-49,774,486 , GRCh38.p12 chr19: 49,068,799-49,271,229 SNRNP70, HRC, 8 more genes
    nsv4321864inversion1nstd166human GRCh37.p13 chr19: 46,657,897-51,634,775 , GRCh38.p12 chr19: 46,154,640-51,131,518 , C5AR1, 288 more genes
    nsv4264304copy number variation1nstd166human GRCh37.p13 chr19: 49,634,695-49,677,638 , GRCh38.p12 chr19: 49,131,438-49,174,381 HRC, TRPM4, 1 more genes
    nsv4258404copy number variation1nstd166human GRCh37.p13 chr19: 49,648,000-49,654,000 , GRCh38.p12 chr19: 49,144,743-49,150,743 HRC, PPFIA3
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