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 404

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099255copy number variation1nstd231human GRCh38.p12 chr1: 192,358,641-201,911,882 , GRCh37 chr1: 192,327,771-201,881,010 CACNA1S, CSRP1, 120 more genes
    nsv7093373copy number variation1nstd102humanUncertain significance GRCh37 chr1: 196,670,448-197,898,389 , GRCh38.p12 chr1: 196,701,318-197,929,259 LHX9, ASPM, 19 more genes
    nsv7044345inversion1nstd229human GRCh38 chr1: 196,256,799-197,729,314 , GRCh37.p13 chr1: 196,225,929-197,698,444 EEF1A1P32, MIR4735, 17 more genes
    nsv6677752copy number variation1nstd229human GRCh38 chr1: 196,925,458-196,942,476 , GRCh37.p13 chr1: 196,894,588-196,911,606 CFHR2, LOC105371675
    nsv6660761copy number variation1nstd229human GRCh38 chr1: 196,929,101-196,944,000 , GRCh37.p13 chr1: 196,898,231-196,913,130 LOC105371675, CFHR2
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6636659copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 189,633,885-199,854,163 , GRCh38.p12 chr1: 189,664,755-199,885,035 F13B, CFH, 88 more genes
    nsv6636303copy number variation1nstd102humanPathogenic GRCh37 chr1: 193,011,753-199,882,947 , GRCh38.p12 chr1: 193,042,623-199,913,819 RPS2P9, ASPM, 60 more genes
    nsv6635686copy number variation1nstd227human GRCh38.p12 chr1: 196,854,170-196,960,180 , GRCh37 chr1: 196,823,300-196,929,310 CFHR2, CFHR4, 2 more genes
    nsv6635240copy number variation3nstd227human GRCh38.p12 chr1: 196,854,170-196,953,730 , GRCh37 chr1: 196,823,300-196,922,860 CFHR2, CFHR4, 2 more genes
    nsv6626146copy number variation1nstd224human GRCh37 chr1: 196,801,025-196,918,605 , GRCh38.p12 chr1: 196,831,895-196,949,475 CFHR1, LOC105371675, 3 more genes
    nsv6626141copy number variation1nstd224human GRCh37 chr1: 196,712,596-196,918,615 , GRCh38.p12 chr1: 196,743,466-196,949,485 CFH, CFHR1, 5 more genes
    nsv6626137copy number variation1nstd224human GRCh37 chr1: 196,711,067-196,920,123 , GRCh38.p12 chr1: 196,741,937-196,950,993 CFH, CFHR1, 5 more genes
    nsv6626136copy number variation1nstd224human GRCh37 chr1: 196,709,816-196,920,123 , GRCh38.p12 chr1: 196,740,686-196,950,993 CFH, CFHR1, 5 more genes
    nsv6626073copy number variation2nstd224human GRCh37 chr1: 196,794,652-196,918,615 , GRCh38.p12 chr1: 196,825,522-196,949,485 CFHR2, LOC100996886, 3 more genes
    nsv6625723copy number variation1nstd224human GRCh37 chr1: 196,823,300-196,918,605 , GRCh38.p12 chr1: 196,854,170-196,949,475 CFHR2, LOC100996886, 2 more genes
    nsv6625709copy number variation2nstd224human GRCh37 chr1: 196,709,833-196,919,987 , GRCh38.p12 chr1: 196,740,703-196,950,857 CFH, CFHR1, 5 more genes
    nsv6553183inversion1nstd223human GRCh38 chr1: 196,953,465-196,955,870 , GRCh37.p13 chr1: 196,922,595-196,925,000 CFHR2
    nsv6328837copy number variation1nstd223human GRCh38 chr1: 196,925,456-196,942,473 , GRCh37.p13 chr1: 196,894,586-196,911,603 CFHR2, LOC105371675
    nsv6327650copy number variation1nstd223human GRCh38 chr1: 196,941,601-196,943,300 , GRCh37.p13 chr1: 196,910,731-196,912,430 CFHR2
    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