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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145797copy number variation1nstd232human GRCh38.p12 chr19: 2,234,061-2,234,148 , GRCh37.p13 chr19: 2,234,060-2,234,147 PLEKHJ1, MIR1227, 1 more genes
    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
    nsv7014639copy number variation1nstd229human GRCh38 chr19: 2,232,724-2,232,837 , GRCh37.p13 chr19: 2,232,723-2,232,836 DOT1L, MIR1227, 1 more genes
    nsv6998585copy number variation1nstd229human GRCh38 chr19: 2,233,333-2,233,367 , GRCh37.p13 chr19: 2,233,332-2,233,366 PLEKHJ1, MIR1227
    nsv6517268copy number variation1nstd223human GRCh38 chr19: 2,200,079-2,233,054 , GRCh37.p13 chr19: 2,200,078-2,233,053 PLEKHJ1, MIR1227, 1 more genes
    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
    nsv6285411insertion1nstd214human GRCh38 chr19: 2,233,319-2,233,319 , GRCh37.p13 chr19: 2,233,318-2,233,318 PLEKHJ1, MIR1227
    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
    nsv6102682inversion1nstd212human GRCh38 chr19: 871,904-2,377,665 , GRCh37.p13 chr19: 871,904-2,377,663 AMH, ATP5F1D, 83 more genes
    nsv5294229copy number variation1nstd204human GRCh38.p13 chr19: 1,717,401-2,347,800 , GRCh37.p13 chr19: 1,717,400-2,347,798 DOT1L, LOC107985278, 32 more genes
    nsv5291342copy number variation1nstd204human GRCh38.p13 chr19: 879,901-2,550,600 , GRCh37.p13 chr19: 879,901-2,550,598 LOC105372240, ELOCP28, 92 more genes
    nsv5014306copy number variation1nstd200human GRCh38 chr19: 2,229,923-2,295,815 , GRCh37.p13 chr19: 2,229,922-2,295,814 MIR4321, MIR6789, 10 more genes
    nsv4676366copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 1,075,192-2,256,387 , GRCh38.p12 chr19: 1,075,193-2,256,388 AMH, ATP5F1D, 64 more genes
    nsv4676346copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,501,271 , GRCh38.p12 chr19: 260,911-3,501,273 AZU1, REEP6, 159 more genes
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