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 124

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054901inversion1nstd229human GRCh38 chr5: 86,506,255-87,299,369 , GRCh37.p13 chr5: 85,802,072-86,595,186 RN7SL629P, MIR4280, 12 more genes
    nsv7053929inversion1nstd229human GRCh38 chr5: 86,672,047-86,816,673 , GRCh37.p13 chr5: 85,967,864-86,112,490 LINC02059
    nsv7053596inversion1nstd229human GRCh38 chr5: 85,730,857-88,063,519 , GRCh37.p13 chr5: 85,026,675-87,359,336 LOC100421863, RPL10AP9, 25 more genes
    nsv7050687inversion1nstd229human GRCh38 chr5: 86,603,498-87,299,362 , GRCh37.p13 chr5: 85,899,315-86,595,179 RPL10AP9, LINC01949, 12 more genes
    nsv7045583inversion1nstd229human GRCh38 chr5: 86,305,164-86,775,367 , GRCh37.p13 chr5: 85,600,982-86,071,184 LINC02059, LOC105379064, 4 more genes
    nsv6775192copy number variation1nstd229human GRCh38 chr5: 86,690,880-86,749,460 , GRCh37.p13 chr5: 85,986,697-86,045,277 LINC02059
    nsv6774383copy number variation1nstd229human GRCh38 chr5: 86,745,249-86,751,093 , GRCh37.p13 chr5: 86,041,066-86,046,910 LINC02059
    nsv6760412copy number variation1nstd229human GRCh38 chr5: 86,127,035-87,005,434 , GRCh37.p13 chr5: 85,422,853-86,301,251 COX7C, LOC100421863, 6 more genes
    nsv6758477copy number variation1nstd229human GRCh38 chr5: 86,716,745-86,749,589 , GRCh37.p13 chr5: 86,012,562-86,045,406 LINC02059
    nsv6636247copy number variation1nstd102humanUncertain significance GRCh37 chr5: 85,849,576-86,109,647 , GRCh38.p12 chr5: 86,553,759-86,813,830 LINC02059, RNU6-804P, 2 more genes
    nsv6630892copy number variation1nstd224human GRCh37 chr5: 86,012,253-86,129,665 , GRCh38.p12 chr5: 86,716,436-86,833,848 LINC02059
    nsv6398739copy number variation1nstd223human GRCh38 chr5: 83,701,679-87,055,970 , GRCh37.p13 chr5: 82,997,498-86,351,787 LOC645261, LOC105379061, 28 more genes
    nsv6313788copy number variation1nstd102humanPathogenic GRCh37 chr5: 82,185,951-90,110,454 , GRCh38.p12 chr5: 82,890,132-90,814,637 RASA1, HAPLN1, 82 more genes
    nsv6136135copy number variation1nstd213human GRCh37 chr5: 85,890,000-86,050,001 , GRCh38.p12 chr5: 86,594,183-86,754,184 COX7C, LINC02059, 2 more genes
    nsv6135438copy number variation1nstd213human GRCh37 chr5: 80,920,000-86,370,001 , GRCh38.p12 chr5: 81,624,181-87,074,184 COX7C, HAPLN1, 56 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135200copy number variation1nstd213human GRCh37 chr5: 76,540,000-94,260,001 , GRCh38.p12 chr5: 77,244,175-94,924,296 ACTBP2, ARSB, 200 more genes
    nsv6006909copy number variation1nstd212human GRCh38 chr5: 86,746,407-86,752,775 , GRCh37.p13 chr5: 86,042,224-86,048,592 LINC02059
    nsv5693379mobile element insertion1nstd211human GRCh38 chr5: 86,748,431-86,748,431 , GRCh37.p13 chr5: 86,044,248-86,044,248 LINC02059
    nsv5090714mobile element insertion1nstd203human GRCh38 chr5: 86,748,415-86,748,431 , GRCh37.p13 chr5: 86,044,232-86,044,248 LINC02059
    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