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 144

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7040236inversion1nstd229human GRCh38 chr6: 111,756,087-112,191,364 , GRCh37.p13 chr6: 112,077,290-112,323,681 TUBE1, FYN, 7 more genes
    nsv6815317copy number variation1nstd229human GRCh38 chr6: 110,458,576-114,390,336 , GRCh37.p13 chr6: 110,779,779-114,711,500 LOC105377956, LOC102724646, 79 more genes
    nsv6814178copy number variation1nstd229human GRCh38 chr6: 112,017,483-112,054,139 , GRCh37.p13 chr6|NW_003871062.1: 15,005-51,661 , GRCh37.p13 chr6: 112,338,686-112,375,342 CCN6
    nsv6809374copy number variation1nstd229human GRCh38 chr6: 112,046,493-112,158,352 , GRCh37.p13 chr6: 112,367,696-112,479,554 , GRCh37.p13 chr6|NW_003871062.1: 44,015-155,873 CCN6, FAM229B, 3 more genes
    nsv6808751copy number variation1nstd229human GRCh38 chr6: 111,950,266-112,105,602 , GRCh37.p13 chr6|NW_003871062.1: 1-103,124 , GRCh37.p13 chr6: 112,323,682-112,426,805 FAM229B, TUBE1, 2 more genes
    nsv6808569copy number variation1nstd229human GRCh38 chr6: 112,061,913-112,067,390 , GRCh37.p13 chr6|NW_003871062.1: 59,435-64,912 , GRCh37.p13 chr6: 112,383,116-112,388,593 CCN6
    nsv6619247copy number variation1nstd223human GRCh38 chr6: 112,017,483-112,054,135 , GRCh37.p13 chr6: 112,338,686-112,375,338 , GRCh37.p13 chr6|NW_003871062.1: 15,005-51,657 CCN6
    nsv6617586copy number variation1nstd223human GRCh38 chr6: 112,060,026-112,060,660 , GRCh37.p13 chr6: 112,381,229-112,381,863 , GRCh37.p13 chr6|NW_003871062.1: 57,548-58,182 CCN6
    nsv6608488copy number variation1nstd223human GRCh38 chr6: 112,058,843-112,059,360 , GRCh37.p13 chr6: 112,380,046-112,380,563 , GRCh37.p13 chr6|NW_003871062.1: 56,365-56,882 CCN6
    nsv6606808copy number variation1nstd223human GRCh38 chr6: 111,642,175-118,933,374 , GRCh37.p13 chr6: 111,963,378-119,254,539 COL10A1, LOC105377952, 106 more genes
    nsv6600080copy number variation1nstd223human GRCh38 chr6: 112,050,622-112,051,017 , GRCh37.p13 chr6|NW_003871062.1: 48,144-48,539 , GRCh37.p13 chr6: 112,371,825-112,372,220 CCN6
    nsv6313858copy number variation1nstd102humanPathogenic GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488 RN7SL509P, LAMA4, 311 more genes
    nsv6313613copy number variation1nstd102humanUncertain significance GRCh37 chr6: 110,472,732-114,762,836 , GRCh38.p12 chr6: 110,151,529-114,441,672 LOC107986522, TUBE1, 87 more genes
    nsv6135228copy number variation1nstd213human GRCh37 chr6: 112,190,000-112,390,001 , GRCh38.p12 chr6: 111,868,797-112,068,798 FYN, CCN6, 4 more genes
    nsv5692964mobile element insertion2nstd211human GRCh38 chr6: 112,068,840-112,068,840 , GRCh37.p13 chr6|NW_003871062.1: 66,362-66,362 , GRCh37.p13 chr6: 112,390,043-112,390,043 TUBE1, CCN6
    nsv5564516copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,796,301-113,083,437 , GRCh38.p12 chr6: 109,475,098-112,762,235 RN7SL617P, METTL24, 67 more genes
    nsv5409290mobile element insertion1nstd206human GRCh38 chr6: 112,068,840-112,068,891 , GRCh37.p13 chr6|NW_003871062.1: 66,362-66,413 , GRCh37.p13 chr6: 112,390,043-112,390,094 TUBE1, CCN6
    nsv5107115mobile element insertion1nstd203human GRCh38 chr6: 112,068,826-112,068,840 , GRCh37.p13 chr6|NW_003871062.1: 66,348-66,362 , GRCh37.p13 chr6: 112,390,029-112,390,043 CCN6, TUBE1
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4768376copy number variation1nstd102humanPathogenic GRCh37 chr6: 98,949,950-114,533,905 , GRCh38.p12 chr6: 98,502,074-114,212,741 LOC101927405, GPR6, 211 more genes
    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