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Items: 1 to 20 of 298

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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
    nsv7074131inversion1nstd229human GRCh38 chr19: 34,477,873-34,665,876 , GRCh37.p13 chr19: 34,968,778-35,156,781 WTIP, ZNF807P, 7 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
    nsv7008907copy number variation1nstd229human GRCh38 chr19: 34,477,872-34,513,105 , GRCh37.p13 chr19: 34,968,777-35,004,010 WTIP
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv6999633copy number variation1nstd229human GRCh38 chr19: 34,478,249-34,480,615 , GRCh37.p13 chr19: 34,969,154-34,971,520 WTIP
    nsv6532275copy number variation1nstd223human GRCh38 chr19: 34,486,653-34,488,610 , GRCh37.p13 chr19: 34,977,558-34,979,515 WTIP
    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
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6054511copy number variation1nstd212human GRCh38 chr19: 34,501,224-34,501,333 , GRCh37.p13 chr19: 34,992,129-34,992,238 WTIP
    nsv5699913mobile element insertion1nstd211human GRCh38 chr19: 34,511,856-34,511,856 , GRCh37.p13 chr19: 35,002,761-35,002,761 WTIP
    nsv5530878copy number variation1nstd206human GRCh38 chr19: 34,481,605-34,481,779 , GRCh37.p13 chr19: 34,972,510-34,972,684 WTIP
    nsv5518017copy number variation1nstd206human GRCh38 chr19: 34,496,560-34,496,648 , GRCh37.p13 chr19: 34,987,465-34,987,553 WTIP
    nsv5427109mobile element insertion1nstd206human GRCh38 chr19: 34,511,856-34,511,907 , GRCh37.p13 chr19: 35,002,761-35,002,812 WTIP
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