U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 189

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148227copy number variation1nstd102humanPathogenic GRCh38 chr14: 102,263,440-106,874,929 , GRCh37.p13 chr14: 102,729,777-107,283,138 TNFAIP2, IGHV4-30-2, 306 more genes
    nsv7094415copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 102,931,627-102,968,819 , GRCh38.p12 chr14: 102,465,290-102,502,482 TECPR2, ANKRD9, 1 more genes
    nsv7094241copy number variation1nstd102humanUncertain significance GRCh37 chr14: 102,442,029-105,861,009 , GRCh38.p12 chr14: 101,975,692-105,394,672 LOC107984670, MARK3, 101 more genes
    nsv7094007copy number variation1nstd102humanUncertain significance GRCh37 chr14: 102,228,231-105,861,009 , GRCh38.p12 chr14: 101,761,894-105,394,672 CLBA1, BAG5, 105 more genes
    nsv7058698inversion1nstd229human GRCh38 chr14: 102,464,915-102,522,991 , GRCh37.p13 chr14: 102,931,252-102,989,328 ANKRD9, LOC105370679, 3 more genes
    nsv6976628copy number variation1nstd229human GRCh38 chr14: 102,397,679-102,817,795 , GRCh37.p13 chr14: 102,864,016-103,284,132 ANKRD9, RPL23AP11, 9 more genes
    nsv6975488copy number variation1nstd229human GRCh38 chr14: 102,463,488-102,718,067 , GRCh37.p13 chr14: 102,929,825-103,184,404 LINC02323, TECPR2, 8 more genes
    nsv6974587copy number variation1nstd229human GRCh38 chr14: 102,488,906-102,712,533 , GRCh37.p13 chr14: 102,955,243-103,178,870 RNU6-244P, LOC105370680, 8 more genes
    nsv6972411copy number variation1nstd229human GRCh38 chr14: 102,502,134-102,502,160 , GRCh37.p13 chr14: 102,968,471-102,968,497 TECPR2, ANKRD9, 1 more genes
    nsv6964833copy number variation1nstd229human GRCh38 chr14: 102,507,201-102,658,900 , GRCh37.p13 chr14: 102,973,538-103,125,237 RCOR1, LOC105370679, 5 more genes
    nsv6960683copy number variation1nstd229human GRCh38 chr14: 102,500,527-102,502,775 , GRCh37.p13 chr14: 102,966,864-102,969,112 ANKRD9, RNU6-244P, 1 more genes
    nsv6960203copy number variation1nstd229human GRCh38 chr14: 102,406,201-102,658,400 , GRCh37.p13 chr14: 102,872,538-103,124,737 RCOR1, ANKRD9, 7 more genes
    nsv6960030copy number variation1nstd229human GRCh38 chr14: 102,380,080-102,868,959 , GRCh37.p13 chr14: 102,846,417-103,335,296 ANKRD9, RCOR1, 10 more genes
    nsv6959186copy number variation1nstd229human GRCh38 chr14: 102,476,958-102,705,297 , GRCh37.p13 chr14: 102,943,295-103,171,634 RNU6-244P, LOC105370680, 8 more genes
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
    nsv6622434copy number variation1nstd224human GRCh37 chr14: 102,958,285-102,974,999 , GRCh38.p12 chr14: 102,491,948-102,508,662 TECPR2, RNU6-244P, 2 more genes
    nsv6622232copy number variation1nstd224human GRCh37 chr14: 102,881,115-103,396,961 , GRCh38.p12 chr14: 102,414,778-102,930,624 RPL23AP11, LOC105370680, 12 more genes
    nsv6621988copy number variation1nstd224human GRCh37 chr14: 102,958,285-103,111,823 , GRCh38.p12 chr14: 102,491,948-102,645,486 TECPR2, RCOR1, 7 more genes
    nsv6503115copy number variation1nstd223human GRCh38 chr14: 102,492,257-102,799,383 , GRCh37.p13 chr14: 102,958,594-103,265,720 RN7SL546P, TECPR2, 9 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center