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Items: 1 to 20 of 227

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144902insertion1nstd232human GRCh37.p13 chr19: 2,247,023-2,247,023 , GRCh38.p12 chr19: 2,247,024-2,247,024 SF3A2
    nsv7137288insertion1nstd232human GRCh37.p13 chr19: 2,247,127-2,247,127 , GRCh38.p12 chr19: 2,247,128-2,247,128 SF3A2
    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
    nsv7095644copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,456,055-2,456,931 , GRCh38.p12 chr19: 1,456,056-2,456,933 APC2, CSNK1G2, 49 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
    nsv7073114inversion1nstd229human GRCh38 chr19: 2,143,875-2,402,071 , GRCh37.p13 chr19: 2,143,874-2,402,069 OAZ1, SF3A2, 15 more genes
    nsv7016706copy number variation1nstd229human GRCh38 chr19: 2,129,001-2,344,100 , GRCh37.p13 chr19: 2,129,000-2,344,098 AP3D1, MIR4321, 14 more genes
    nsv6599008inversion1nstd223human GRCh38 chr19: 2,237,413-2,237,647 , GRCh37.p13 chr19: 2,237,412-2,237,646 SF3A2
    nsv6315518copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-2,256,387 , GRCh38.p12 chr19: 260,911-2,256,388 LOC100420586, RPS15, 113 more genes
    nsv6291606copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,973,753-2,380,699 , GRCh38.p12 chr19: 1,973,754-2,380,701 DOT1L, LOC107985278, 20 more genes
    nsv6289594insertion1nstd214human GRCh38 chr19: 2,247,128-2,247,128 , GRCh37.p13 chr19: 2,247,127-2,247,127 SF3A2
    nsv6288606insertion1nstd214human GRCh38 chr19: 2,247,125-2,247,125 , GRCh37.p13 chr19: 2,247,124-2,247,124 SF3A2
    nsv6196665copy number variation1nstd214human GRCh38 chr19: 2,242,081-2,242,164 , GRCh37.p13 chr19: 2,242,080-2,242,163 SF3A2
    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
    nsv6107788insertion1nstd212human GRCh38 chr19: 2,247,131-2,247,131 , GRCh37.p13 chr19: 2,247,130-2,247,130 SF3A2
    nsv6102682inversion1nstd212human GRCh38 chr19: 871,904-2,377,665 , GRCh37.p13 chr19: 871,904-2,377,663 AMH, ATP5F1D, 83 more genes
    nsv6046357copy number variation1nstd212human GRCh38 chr19: 2,242,119-2,242,202 , GRCh37.p13 chr19: 2,242,118-2,242,201 SF3A2
    nsv5945000copy number variation1nstd209human GRCh38 chr19: 2,242,140-2,242,223 , GRCh37.p13 chr19: 2,242,139-2,242,222 SF3A2
    nsv5943865copy number variation1nstd209human GRCh38 chr19: 2,247,088-2,247,165 , GRCh37.p13 chr19: 2,247,087-2,247,164 SF3A2
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