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 114

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6450829copy number variation1nstd223human GRCh38 chr9: 116,398,199-116,398,917 , GRCh37.p13 chr9: 119,160,478-119,161,196 PAPPA, PAPPA-AS1
    nsv6439926copy number variation1nstd223human GRCh38 chr9: 116,399,296-116,399,883 , GRCh37.p13 chr9: 119,161,575-119,162,162 PAPPA, PAPPA-AS1
    nsv6438862copy number variation1nstd223human GRCh38 chr9: 116,340,232-116,556,451 , GRCh37.p13 chr9: 119,102,511-119,318,730 PAPPA-AS1, PAPPA, 2 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6314001copy number variation1nstd102humanPathogenic GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954 LOC105376244, RN7SL187P, 286 more genes
    nsv6313908copy number variation1nstd102humanUncertain significance GRCh37 chr9: 116,506,015-119,942,279 , GRCh38.p12 chr9: 113,743,735-117,180,000 LOC105376224, TEX53, 45 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6291271copy number variation1nstd102humanUncertain significance GRCh37 chr9: 119,116,147-119,313,250 , GRCh38.p12 chr9: 116,353,868-116,550,971 PAPPA-AS1, ASTN2-AS1, 2 more genes
    nsv6290238copy number variation1nstd102humanUncertain significance GRCh37 chr9: 117,853,848-124,633,077 , GRCh38.p12 chr9: 115,091,569-121,870,798 LINC00474, LOC107987123, 72 more genes
    nsv6137437copy number variation1nstd213human GRCh37 chr9: 118,910,000-119,320,001 , GRCh38.p12 chr9: 116,147,721-116,557,722 PAPPA, ASTN2, 2 more genes
    nsv6136728copy number variation1nstd213human GRCh37 chr9: 117,920,000-120,020,001 , GRCh38.p12 chr9: 115,157,721-117,257,722 LINC00474, SNORA70C, 19 more genes
    nsv5317389copy number variation1nstd204human GRCh38.p13 chr9: 116,311,558-116,419,432 , GRCh37.p13 chr9: 119,073,837-119,181,711 PAPPA, PAPPA-AS1
    nsv5257117copy number variation1nstd204human GRCh38.p13 chr9: 116,311,601-116,419,700 , GRCh37.p13 chr9: 119,073,880-119,181,979 PAPPA, PAPPA-AS1
    nsv5255548copy number variation1nstd204human GRCh38.p13 chr9: 116,380,052-116,413,931 , GRCh37.p13 chr9: 119,142,331-119,176,210 PAPPA, PAPPA-AS1
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4974855copy number variation1nstd200human GRCh38 chr9: 116,364,297-116,539,661 , GRCh37.p13 chr9: 119,126,576-119,301,940 PAPPA-AS1, PAPPA, 2 more genes
    nsv4974854copy number variation1nstd200human GRCh38 chr9: 116,196,105-116,418,127 , GRCh37.p13 chr9: 118,958,384-119,180,406 PAPPA-AS1, PAPPA
    nsv4845736copy number variation1nstd200human GRCh37 chr9: 119,073,847-119,181,711 , GRCh38.p12 chr9: 116,311,568-116,419,432 PAPPA, PAPPA-AS1
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

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