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 383

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5947690insertion1nstd209human GRCh38 chr6: 111,764,216-111,764,216 , GRCh37.p13 chr6: 112,085,419-112,085,419 FYN
    nsv5727530mobile element insertion1nstd211human GRCh38 chr6: 111,800,542-111,800,542 , GRCh37.p13 chr6: 112,121,745-112,121,745 FYN
    nsv5684182mobile element insertion1nstd211human GRCh38 chr6: 111,873,940-111,873,940 , GRCh37.p13 chr6: 112,195,143-112,195,143 FYN, LOC102724646
    nsv5683299mobile element insertion2nstd211human GRCh38 chr6: 111,828,587-111,828,587 , GRCh37.p13 chr6: 112,149,790-112,149,790 FYN
    nsv5681003mobile element insertion1nstd211human GRCh38 chr6: 111,689,024-111,689,024 , GRCh37.p13 chr6: 112,010,227-112,010,227 LOC105377945, FYN
    nsv5679973mobile element insertion1nstd211human GRCh38 chr6: 111,843,381-111,843,381 , GRCh37.p13 chr6: 112,164,584-112,164,584 FYN
    nsv5639928insertion2nstd207human GRCh38 chr6: 111,773,616-111,773,616 , GRCh37.p13 chr6: 112,094,819-112,094,819 FYN
    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
    nsv5563916mobile element insertion1nstd206human GRCh38 chr6: 111,800,492-111,800,542 , GRCh37.p13 chr6: 112,121,695-112,121,745 FYN
    nsv5563424sequence alteration1nstd206human GRCh38 chr6: 111,815,965-111,872,169 , GRCh37.p13 chr6: 112,137,168-112,193,372 FYN, LOC102724646
    nsv5552944insertion1nstd206human GRCh38 chr6: 111,777,363-111,777,405 , GRCh37.p13 chr6: 112,098,566-112,098,608 FYN
    nsv5551335insertion1nstd206human GRCh38 chr6: 111,828,587-111,828,603 , GRCh37.p13 chr6: 112,149,790-112,149,806 FYN
    nsv5545363insertion1nstd206human GRCh38 chr6: 111,828,587-111,828,638 , GRCh37.p13 chr6: 112,149,790-112,149,841 FYN
    nsv5539777insertion1nstd206human GRCh38 chr6: 111,773,499-111,773,526 , GRCh37.p13 chr6: 112,094,702-112,094,729 FYN
    nsv5471688copy number variation1nstd206human GRCh38 chr6: 111,850,856-111,854,381 , GRCh37.p13 chr6: 112,172,059-112,175,584 FYN
    nsv5463482copy number variation1nstd206human GRCh38 chr6: 111,672,664-111,672,753 , GRCh37.p13 chr6: 111,993,867-111,993,956 FYN
    nsv5454851copy number variation1nstd206human GRCh38 chr6: 111,716,667-111,716,763 , GRCh37.p13 chr6: 112,037,870-112,037,966 FYN
    nsv5411878mobile element insertion1nstd206human GRCh38 chr6: 111,689,024-111,689,070 , GRCh37.p13 chr6: 112,010,227-112,010,273 FYN, LOC105377945
    nsv5411676mobile element insertion1nstd206human GRCh38 chr6: 111,843,381-111,843,432 , GRCh37.p13 chr6: 112,164,584-112,164,635 FYN
    nsv5402444mobile element insertion1nstd206human GRCh38 chr6: 111,873,940-111,873,991 , GRCh37.p13 chr6: 112,195,143-112,195,194 LOC102724646, FYN
    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