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 202

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099223copy number variation1nstd231human GRCh38.p12 chr1: 108,551,579-110,710,631 , GRCh37 chr1: 109,094,201-111,253,253 ALX3, AMPD2, 74 more genes
    nsv7095739copy number variation1nstd102humanPathogenic GRCh37 chr1: 108,679,275-111,674,176 , GRCh38.p12 chr1: 108,136,653-111,131,554 RPL7L1P21, GSTM4, 90 more genes
    nsv6639791copy number variation1nstd229human GRCh38 chr1: 109,098,301-109,290,000 , GRCh37.p13 chr1: 109,640,923-109,832,622 CELSR2, ELAPOR1, 5 more genes
    nsv6639741copy number variation1nstd229human GRCh38 chr1: 109,097,401-109,356,500 , GRCh37.p13 chr1: 109,640,023-109,899,122 ELAPOR1, CELSR2, 8 more genes
    nsv6639736copy number variation1nstd229human GRCh38 chr1: 108,994,101-109,359,800 , GRCh37.p13 chr1: 109,536,723-109,902,422 LOC100420092, PSRC1, 14 more genes
    nsv6639721copy number variation1nstd229human GRCh38 chr1: 108,756,469-109,410,478 , GRCh37.p13 chr1: 109,299,091-109,953,100 PSMA5, STXBP3, 24 more genes
    nsv6639663copy number variation1nstd229human GRCh38 chr1: 109,281,561-109,282,089 , GRCh37.p13 chr1: 109,824,183-109,824,711 PSRC1
    nsv6639662copy number variation1nstd229human GRCh38 chr1: 109,263,357-109,279,418 , GRCh37.p13 chr1: 109,805,979-109,822,040 PSRC1, CELSR2
    nsv6639661copy number variation1nstd229human GRCh38 chr1: 109,252,523-109,304,250 , GRCh37.p13 chr1: 109,795,145-109,846,872 MYBPHL, PSRC1, 1 more genes
    nsv6639543copy number variation1nstd229human GRCh38 chr1: 108,780,593-109,355,741 , GRCh37.p13 chr1: 109,323,215-109,898,363 STXBP3, TMEM167B-DT, 22 more genes
    nsv6639418copy number variation1nstd229human GRCh38 chr1: 108,842,021-109,295,218 , GRCh37.p13 chr1: 109,384,643-109,837,840 PSRC1, AKNAD1, 19 more genes
    nsv6639338copy number variation1nstd229human GRCh38 chr1: 109,276,993-109,279,341 , GRCh37.p13 chr1: 109,819,615-109,821,963 PSRC1
    nsv6639337copy number variation1nstd229human GRCh38 chr1: 109,271,001-109,287,334 , GRCh37.p13 chr1: 109,813,623-109,829,956 PSRC1, CELSR2
    nsv6639335copy number variation1nstd229human GRCh38 chr1: 109,251,299-109,288,477 , GRCh37.p13 chr1: 109,793,921-109,831,099 CELSR2, PSRC1
    nsv6639331copy number variation1nstd229human GRCh38 chr1: 109,201,801-109,290,000 , GRCh37.p13 chr1: 109,744,423-109,832,622 SARS1, PSRC1, 2 more genes
    nsv6636931copy number variation1nstd102humanUncertain significance GRCh37 chr1: 109,371,874-109,906,234 , GRCh38.p12 chr1: 108,829,252-109,363,612 CELSR2, TAF13, 21 more genes
    nsv6636625copy number variation1nstd102humanUncertain significance GRCh37 chr1: 109,350,810-109,838,970 , GRCh38.p12 chr1: 108,808,188-109,296,348 CELSR2, RANP5, 21 more genes
    nsv6322587copy number variation1nstd223human GRCh38 chr1: 109,166,504-109,284,128 , GRCh37.p13 chr1: 109,709,126-109,826,750 PSRC1, CELSR2, 2 more genes
    nsv6313675copy number variation1nstd102humanPathogenic GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309 LINC01307, FTLP17, 320 more genes
    nsv6297919copy number variation1nstd186human GRCh37 chr1: 109,822,780-109,823,015 , GRCh38.p12 chr1: 109,280,158-109,280,393 PSRC1
    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