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Items: 1 to 20 of 98

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7068649inversion1nstd229human GRCh38 chr19: 4,313,135-7,007,201 , GRCh37.p13 chr19: 4,313,132-7,007,212 CAPS, SH2D3A, 93 more genes
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7066921inversion1nstd229human GRCh38 chr19: 4,809,260-7,077,959 , GRCh37.p13 chr19: 4,809,272-7,077,970 MLLT1, GPR108, 74 more genes
    nsv6999737copy number variation1nstd229human GRCh38 chr19: 5,366,371-5,553,641 , GRCh37.p13 chr19: 5,366,382-5,553,652 ZNRF4
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6595723inversion1nstd223human GRCh38 chr19: 4,740,732-5,531,305 , GRCh37.p13 chr19: 4,740,744-5,531,316 UHRF1, ZNRF4, 12 more genes
    nsv6144904copy number variation1nstd206human GRCh38 chr19: 5,448,894-5,460,055 , GRCh37.p13 chr19: 5,448,905-5,460,066 ZNRF4
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133468copy number variation1nstd213human GRCh37 chr19: 2,040,000-7,300,001 , GRCh38.p12 chr19: 2,040,001-7,299,990 TLE5, AMH, 192 more genes
    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
    nsv5014411copy number variation1nstd200human GRCh38 chr19: 5,448,883-5,460,086 , GRCh37.p13 chr19: 5,448,894-5,460,097 ZNRF4
    nsv4676355copy number variation1nstd102humanUncertain significance GRCh37 chr19: 5,310,645-5,515,780 , GRCh38.p12 chr19: 5,310,634-5,515,769 PTPRS, LOC105372252, 1 more genes
    nsv4413749copy number variation1nstd174human GRCh37 chr19: 5,310,647-5,495,940 , GRCh38.p12 chr19: 5,310,636-5,495,929 LOC105372252, PTPRS, 1 more genes
    nsv4266044copy number variation1nstd166human GRCh37.p13 chr19: 5,448,945-5,460,011 , GRCh38.p12 chr19: 5,448,934-5,460,000 ZNRF4
    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
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