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 574

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130341insertion1nstd186human GRCh37 chr14: 60,216,823-60,216,865 , GRCh38.p12 chr14: 59,750,105-59,750,147 RTN1
    nsv6113232mobile element insertion1nstd186human GRCh37 chr14: 60,126,672-60,126,672 , GRCh38.p12 chr14: 59,659,954-59,659,954 RTN1
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5979921insertion1nstd209human GRCh38 chr14: 59,750,232-59,750,232 , GRCh37.p13 chr14: 60,216,950-60,216,950 RTN1
    nsv5947184copy number variation1nstd209human GRCh38 chr14: 59,661,508-59,667,278 , GRCh37.p13 chr14: 60,128,226-60,133,996 RTN1
    nsv5946780copy number variation1nstd209human GRCh38 chr14: 59,749,315-59,749,386 , GRCh37.p13 chr14: 60,216,033-60,216,104 RTN1
    nsv5940148copy number variation1nstd209human GRCh38 chr14: 59,687,351-59,687,462 , GRCh37.p13 chr14: 60,154,069-60,154,180 RTN1
    nsv5938566copy number variation1nstd209human GRCh38 chr14: 59,750,086-59,750,690 , GRCh37.p13 chr14: 60,216,804-60,217,408 RTN1
    nsv5935131copy number variation1nstd209human GRCh38 chr14: 59,783,845-59,783,951 , GRCh37.p13 chr14: 60,250,563-60,250,669 RTN1
    nsv5930535copy number variation1nstd209human GRCh38 chr14: 59,712,694-59,715,607 , GRCh37.p13 chr14: 60,179,412-60,182,325 RTN1
    nsv5864164copy number variation1nstd209human GRCh38 chr14: 59,712,751-59,715,650 , GRCh37.p13 chr14: 60,179,469-60,182,368 RTN1
    nsv5848646copy number variation1nstd209human GRCh38 chr14: 59,661,412-59,667,244 , GRCh37.p13 chr14: 60,128,130-60,133,962 RTN1
    nsv5727129mobile element insertion2nstd211human GRCh38 chr14: 59,774,616-59,774,616 , GRCh37.p13 chr14: 60,241,334-60,241,334 RTN1
    nsv5713548mobile element insertion2nstd211human GRCh38 chr14: 59,703,411-59,703,411 , GRCh37.p13 chr14: 60,170,129-60,170,129 RTN1
    nsv5704060mobile element insertion1nstd211human GRCh38 chr14: 59,654,925-59,654,925 , GRCh37.p13 chr14: 60,121,643-60,121,643 RTN1
    nsv5703832mobile element insertion1nstd211human GRCh38 chr14: 59,837,397-59,837,397 , GRCh37.p13 chr14: 60,304,115-60,304,115 RTN1
    nsv5703611mobile element insertion1nstd211human GRCh38 chr14: 59,749,369-59,749,369 , GRCh37.p13 chr14: 60,216,087-60,216,087 RTN1
    nsv5697173mobile element insertion2nstd211human GRCh38 chr14: 59,659,969-59,659,969 , GRCh37.p13 chr14: 60,126,687-60,126,687 RTN1
    nsv5662184insertion1nstd207human GRCh38 chr14: 59,750,212-59,750,212 , GRCh37.p13 chr14: 60,216,930-60,216,930 RTN1
    nsv5662060insertion1nstd207human GRCh38 chr14: 59,750,329-59,750,329 , GRCh37.p13 chr14: 60,217,047-60,217,047 RTN1
    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