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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5942775copy number variation1nstd209human GRCh38 chr19: 2,865,023-7,153,898 , GRCh37.p13 chr19: 2,865,021-7,153,909 , GNA15-DT, 159 more genes
    nsv5527803copy number variation1nstd206human GRCh38 chr19: 5,870,750-5,871,882 , GRCh37.p13 chr19: 5,870,761-5,871,893 FUT5
    nsv5297161copy number variation1nstd204human GRCh38.p13 chr19: 5,868,901-5,898,900 , GRCh37.p13 chr19: 5,868,912-5,898,911 NDUFA11, FUT5
    nsv5285813copy number variation1nstd204human GRCh38.p13 chr19: 5,731,901-6,700,600 , GRCh37.p13 chr19: 5,731,912-6,700,611 MIR6885, LOC390877, 38 more genes
    nsv5029225copy number variation1nstd200human GRCh38 chr19: 5,870,751-5,874,600 , GRCh37.p13 chr19: 5,870,762-5,874,611 FUT5
    nsv5027450copy number variation1nstd200human GRCh38 chr19: 5,870,790-5,871,882 , GRCh37.p13 chr19: 5,870,801-5,871,893 FUT5
    nsv5014416copy number variation1nstd200human GRCh38 chr19: 5,519,830-5,914,524 , GRCh37.p13 chr19: 5,519,841-5,914,535 FUT5, CATSPERD, 19 more genes
    nsv4852750copy number variation1nstd200human GRCh37 chr19: 5,870,773-5,871,923 , GRCh38.p12 chr19: 5,870,762-5,871,912 FUT5
    nsv4271849copy number variation1nstd166human GRCh37.p13 chr19: 5,869,912-5,871,792 , GRCh38.p12 chr19: 5,869,901-5,871,781 FUT5
    nsv4268514copy number variation1nstd166human GRCh37.p13 chr19: 5,852,000-5,867,000 , GRCh38.p12 chr19: 5,851,989-5,866,989 LOC101928844, FUT5
    nsv4261093copy number variation1nstd166human GRCh37.p13 chr19: 5,838,500-5,867,000 , GRCh38.p12 chr19: 5,838,489-5,866,989 FUT3, FUT6, 2 more genes
    nsv3958618copy number variation1nstd168human GRCh38 chr19: 5,857,040-5,890,398 , GRCh37.p13 chr19: 5,857,051-5,890,409 FUT5, LOC101928844, 1 more genes
    nsv3924480copy number variation1nstd102humanUncertain significance NCBI36 chr19: 5,401,983-6,486,595 , GRCh37.p13 chr19: 5,450,983-6,535,595 , GRCh38.p12 chr19: 5,450,972-6,535,584 TINCR, SAFB2, 42 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
    nsv3923313copy number variation1nstd102humanPathogenic GRCh37 chr19: 4,934,897-6,501,653 , GRCh38 chr19: 4,934,885-6,501,642 , NCBI36 chr19: 4,885,897-6,452,653 LOC105372253, FUT3, 47 more genes
    nsv3914351copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555 SEMA6B, RANBP3-DT, 299 more genes
    nsv3913242copy number variation1nstd102humanUncertain significance NCBI36 chr19: 5,586,385-5,818,934 , GRCh37.p13 chr19: 5,635,385-5,867,934 , GRCh38.p12 chr19: 5,635,374-5,867,923 FUT3, RPL36, 12 more genes
    nsv3907907copy number variation1nstd102humanBenign GRCh37 chr19: 5,655,792-5,867,913 , GRCh38.p12 chr19: 5,655,781-5,867,902 NRTN, FUT5, 12 more genes
    nsv3904954copy number variation1nstd102humanBenign GRCh37 chr19: 5,455,422-5,995,450 , GRCh38.p12 chr19: 5,455,411-5,995,439 NDUFA11, CATSPERD, 22 more genes
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