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Items: 1 to 20 of 184

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098718copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,206,913-3,771,740 , GRCh38.p12 chr19: 1,206,914-3,771,742 GIPC3, GNG7, 117 more genes
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 ATP5F1D, LOC102723798, 204 more genes
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7009437copy number variation1nstd229human GRCh38 chr19: 3,753,078-3,753,827 , GRCh37.p13 chr19: 3,753,076-3,753,825 APBA3
    nsv7002392copy number variation1nstd229human GRCh38 chr19: 3,757,601-3,761,513 , GRCh37.p13 chr19: 3,757,599-3,761,511 LOC105372248, MRPL54, 1 more genes
    nsv7001690copy number variation1nstd229human GRCh38 chr19: 3,757,834-3,759,576 , GRCh37.p13 chr19: 3,757,832-3,759,574 APBA3
    nsv6624864copy number variation1nstd224human GRCh37 chr19: 3,586,471-4,217,207 , GRCh38.p12 chr19: 3,586,473-4,217,210 MAP2K2, ZFR2, 24 more genes
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6519169copy number variation1nstd223human GRCh38 chr19: 3,762,083-3,764,755 , GRCh37.p13 chr19: 3,762,081-3,764,753 MRPL54, APBA3, 1 more genes
    nsv6517546copy number variation1nstd223human GRCh38 chr19: 3,742,712-3,764,756 , GRCh37.p13 chr19: 3,742,710-3,764,754 LOC105372248, MRPL54, 2 more genes
    nsv6291587copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,501,624-5,357,124 , GRCh38.p12 chr19: 3,501,626-5,357,113 RN7SL202P, EIF1P6, 67 more genes
    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
    nsv6129479insertion1nstd186human GRCh38.p12 chr19: 3,762,015-3,762,057 , GRCh37 chr19: 3,762,013-3,762,055 APBA3, MRPL54, 1 more genes
    nsv5978909insertion1nstd209human GRCh38 chr19: 3,762,006-3,762,006 , GRCh37.p13 chr19: 3,762,004-3,762,004 APBA3, MRPL54, 1 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
    nsv5707954mobile element insertion2nstd211human GRCh38 chr19: 3,762,015-3,762,015 , GRCh37.p13 chr19: 3,762,013-3,762,013 APBA3, MRPL54, 1 more genes
    nsv5662610insertion1nstd207human GRCh38 chr19: 3,762,006-3,762,006 , GRCh37.p13 chr19: 3,762,004-3,762,004 APBA3, MRPL54, 1 more genes
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