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 416

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977326inversion1nstd209human GRCh38 chr5: 176,286,704-177,635,736 , GRCh37.p13 chr5: 175,713,707-177,062,737 , CLTB, 46 more genes
    nsv5965964insertion1nstd209human GRCh38 chr5: 176,557,683-176,557,683 , GRCh37.p13 chr5: 175,984,684-175,984,684 CDHR2
    nsv5955917insertion1nstd209human GRCh38 chr5: 176,592,101-176,592,101 , GRCh37.p13 chr5: 176,019,102-176,019,102 CDHR2
    nsv5902461copy number variation1nstd209human GRCh38 chr5: 176,591,689-176,591,824 , GRCh37.p13 chr5: 176,018,690-176,018,825 CDHR2
    nsv5901718copy number variation1nstd209human GRCh38 chr5: 172,153,284-177,326,767 , GRCh37.p13 chr5: 171,580,288-176,753,768 , LOC107986487, 114 more genes
    nsv5890306copy number variation1nstd209human GRCh38 chr5: 176,591,762-176,592,092 , GRCh37.p13 chr5: 176,018,763-176,019,093 CDHR2
    nsv5890062copy number variation1nstd209human GRCh38 chr5: 176,061,658-178,007,127 , GRCh37.p13 chr5: 175,488,661-177,434,128 , DBN1, 65 more genes
    nsv5727055mobile element insertion1nstd211human GRCh38 chr5: 176,548,199-176,548,199 , GRCh37.p13 chr5: 175,975,200-175,975,200 CDHR2, RN7SL684P
    nsv5638367insertion2nstd207human GRCh38 chr5: 176,591,689-176,591,689 , GRCh37.p13 chr5: 176,018,690-176,018,690 CDHR2
    nsv5635829insertion1nstd207human GRCh38 chr5: 176,592,096-176,592,096 , GRCh37.p13 chr5: 176,019,097-176,019,097 CDHR2
    nsv5633991insertion1nstd207human GRCh38 chr5: 176,557,682-176,557,682 , GRCh37.p13 chr5: 175,984,683-175,984,683 CDHR2
    nsv5629969insertion1nstd207human GRCh38 chr5: 176,591,949-176,591,949 , GRCh37.p13 chr5: 176,018,950-176,018,950 CDHR2
    nsv5627868insertion1nstd207human GRCh38 chr5: 176,591,959-176,591,959 , GRCh37.p13 chr5: 176,018,960-176,018,960 CDHR2
    nsv5626384insertion1nstd207human GRCh38 chr5: 176,592,092-176,592,092 , GRCh37.p13 chr5: 176,019,093-176,019,093 CDHR2
    nsv5624926insertion1nstd207human GRCh38 chr5: 176,591,760-176,591,760 , GRCh37.p13 chr5: 176,018,761-176,018,761 CDHR2
    nsv5579876copy number variation1nstd207human GRCh38 chr5: 176,591,689-176,591,824 , GRCh37.p13 chr5: 176,018,690-176,018,825 CDHR2
    nsv5564636copy number variation1nstd207human GRCh38 chr5: 176,592,197-176,592,288 , GRCh37.p13 chr5: 176,019,198-176,019,289 CDHR2
    nsv5562210mobile element insertion1nstd206human GRCh38 chr5: 176,548,199-176,548,250 , GRCh37.p13 chr5: 175,975,200-175,975,251 CDHR2, RN7SL684P
    nsv5534403insertion1nstd206human GRCh38 chr5: 176,557,683-176,557,686 , GRCh37.p13 chr5: 175,984,684-175,984,687 CDHR2
    nsv5473597copy number variation1nstd206human GRCh38 chr5: 176,561,776-176,567,567 , GRCh37.p13 chr5: 175,988,777-175,994,568 CDHR2
    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