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Items: 1 to 20 of 145

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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
    nsv5946118copy number variation1nstd209human GRCh38 chr19: 5,957,002-5,957,052 , GRCh37.p13 chr19: 5,957,013-5,957,063 RANBP3
    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
    nsv5524173copy number variation1nstd206human GRCh38 chr19: 5,974,085-5,974,137 , GRCh37.p13 chr19: 5,974,096-5,974,148 RANBP3
    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
    nsv5174828mobile element insertion1nstd203human GRCh38 chr19: 5,927,391-5,927,404 , GRCh37.p13 chr19: 5,927,402-5,927,415 RANBP3
    nsv5161493mobile element insertion1nstd203human GRCh38 chr19: 5,937,056-5,937,056 , GRCh37.p13 chr19: 5,937,067-5,937,067 RANBP3
    nsv5029226copy number variation1nstd200human GRCh38 chr19: 5,935,243-5,936,915 , GRCh37.p13 chr19: 5,935,254-5,936,926 RANBP3
    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
    nsv4727911copy number variation1nstd197human GRCh38.p12 chr19: 5,914,222-5,914,740 , GRCh37 chr19: 5,914,233-5,914,751 CAPS, RANBP3
    nsv4676137copy number variation1nstd102humanUncertain significance GRCh37 chr19: 5,949,772-6,699,729 , GRCh38.p12 chr19: 5,949,761-6,699,718 MIR6885, LOC390877, 27 more genes
    nsv4550768insertion1nstd166human GRCh37.p13 chr19: 5,927,402-5,927,402 , GRCh38.p12 chr19: 5,927,391-5,927,391 RANBP3
    nsv4504739mobile element insertion1nstd166human GRCh37.p13 chr19: 5,944,863-5,944,863 , GRCh38.p12 chr19: 5,944,852-5,944,852 RANBP3
    nsv4502198mobile element insertion1nstd166human GRCh37.p13 chr19: 5,932,685-5,932,685 , GRCh38.p12 chr19: 5,932,674-5,932,674 RANBP3
    nsv4269543copy number variation1nstd166human GRCh37.p13 chr19: 5,937,046-5,937,105 , GRCh38.p12 chr19: 5,937,035-5,937,094 RANBP3
    nsv4257023copy number variation1nstd166human GRCh37.p13 chr19: 5,971,477-5,975,986 , GRCh38.p12 chr19: 5,971,466-5,975,975 RANBP3
    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
    nsv3918411copy number variation1nstd102humanUncertain significance GRCh38 chr19: 5,905,175-6,916,287 , GRCh37 chr19: 5,905,186-6,916,298 , NCBI36 chr19: 5,856,186-6,867,298 CAPS, MIR6790, 36 more genes
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