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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095478copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407 NFKBID, LRP3, 141 more genes
    nsv7074671inversion1nstd229human GRCh38 chr19: 33,126,299-36,006,645 , GRCh37.p13 chr19: 33,617,205-36,497,547 , ZNF30, 120 more genes
    nsv7074279inversion1nstd229human GRCh38 chr19: 33,135,428-36,017,833 , GRCh37.p13 chr19: 33,626,334-36,508,735 , PSENEN, 122 more genes
    nsv7008965copy number variation1nstd229human GRCh38 chr19: 34,325,427-34,510,322 , GRCh37.p13 chr19: 34,816,332-35,001,227 RN7SL154P, WTIP, 4 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7001722copy number variation1nstd229human GRCh38 chr19: 34,438,571-34,438,817 , GRCh37.p13 chr19: 34,929,476-34,929,722 UBA2
    nsv6597840inversion1nstd223human GRCh38 chr19: 34,435,566-34,436,579 , GRCh37.p13 chr19: 34,926,471-34,927,484 UBA2
    nsv6529359copy number variation1nstd223human GRCh38 chr19: 34,325,427-34,510,321 , GRCh37.p13 chr19: 34,816,332-35,001,226 GPI, GARRE1, 4 more genes
    nsv6527355copy number variation1nstd223human GRCh38 chr19: 34,454,954-34,500,303 , GRCh37.p13 chr19: 34,945,859-34,991,208 WTIP, UBA2
    nsv6314074copy number variation1nstd102humanUncertain significance GRCh37 chr19: 32,827,535-35,263,640 , GRCh38.p12 chr19: 32,336,629-34,772,735 LOC100130632, CEP89, 59 more genes
    nsv6291822copy number variation1nstd102humanPathogenic GRCh38 chr19: 34,469,754-34,644,767 , GRCh37.p13 chr19: 34,960,659-35,135,672 UBA2, WTIP, 7 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6222608copy number variation1nstd214human GRCh38 chr19: 34,442,189-34,442,258 , GRCh37.p13 chr19: 34,933,094-34,933,163 UBA2
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6108772insertion1nstd212human GRCh38 chr19: 34,442,441-34,442,441 , GRCh37.p13 chr19: 34,933,346-34,933,346 UBA2
    nsv5947541copy number variation1nstd209human GRCh38 chr19: 34,437,365-34,437,499 , GRCh37.p13 chr19: 34,928,270-34,928,404 UBA2
    nsv5374033translocation1nstd200human GRCh38 chr12: 21,439,055-21,439,055 , GRCh38 chr19: 34,469,890-34,469,890 , GRCh37.p13 chr19: 34,960,795-34,960,795 , GRCh37.p13 chr12: 21,591,989-21,591,989 UBA2, PYROXD1
    nsv5195733mobile element insertion1nstd203human GRCh38 chr19: 34,443,771-34,443,781 , GRCh37.p13 chr19: 34,934,676-34,934,686 UBA2
    nsv5027668copy number variation1nstd200human GRCh38 chr19: 34,465,417-34,466,086 , GRCh37.p13 chr19: 34,956,322-34,956,991 UBA2
    nsv4575514mobile element insertion1nstd166human GRCh37.p13 chr19: 34,934,676-34,934,676 , GRCh38.p12 chr19: 34,443,771-34,443,771 UBA2
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