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Items: 1 to 20 of 215

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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
    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
    nsv7010117copy number variation1nstd229human GRCh38 chr19: 2,257,376-2,257,794 , GRCh37.p13 chr19: 2,257,375-2,257,793 JSRP1
    nsv6532683copy number variation1nstd223human GRCh38 chr19: 2,257,926-2,259,163 , GRCh37.p13 chr19: 2,257,925-2,259,162 JSRP1
    nsv6529963copy number variation1nstd223human GRCh38 chr19: 2,260,041-2,261,127 , GRCh37.p13 chr19: 2,260,040-2,261,126 JSRP1
    nsv6524415copy number variation1nstd223human GRCh38 chr19: 2,259,105-2,262,436 , GRCh37.p13 chr19: 2,259,104-2,262,435 JSRP1
    nsv6522789copy number variation1nstd223human GRCh38 chr19: 2,257,472-2,257,887 , GRCh37.p13 chr19: 2,257,471-2,257,886 JSRP1
    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
    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
    nsv5534220insertion1nstd206human GRCh38 chr19: 2,254,905-2,254,952 , GRCh37.p13 chr19: 2,254,904-2,254,951 JSRP1
    nsv5530261copy number variation1nstd206human GRCh38 chr19: 2,257,577-2,259,230 , GRCh37.p13 chr19: 2,257,576-2,259,229 JSRP1
    nsv5380255translocation1nstd200human GRCh38 chr19: 2,260,165-2,260,165 , GRCh38 chr19: 2,261,585-2,261,585 , GRCh37.p13 chr19: 2,261,584-2,261,584 , GRCh37.p13 chr19: 2,260,164-2,260,164 JSRP1
    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
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