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 679

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965505insertion1nstd209human GRCh38 chr5: 96,899,022-96,899,022 , GRCh37.p13 chr5: 96,234,726-96,234,726 ERAP1, ERAP2
    nsv5958985insertion1nstd209human GRCh38 chr5: 96,805,012-96,805,012 , GRCh37.p13 chr5: 96,140,715-96,140,715 ERAP1
    nsv5951315insertion1nstd209human GRCh38 chr5: 96,856,349-96,856,349 , GRCh37.p13 chr5: 96,192,052-96,192,052 ERAP1
    nsv5907322copy number variation1nstd209human GRCh38 chr5: 96,916,671-96,916,808 , GRCh37.p13 chr5: 96,252,375-96,252,512 ERAP2, ERAP1
    nsv5905191copy number variation1nstd209human GRCh38 chr5: 96,911,971-96,922,055 , GRCh37.p13 chr5: 96,247,675-96,257,759 ERAP1, ERAP2
    nsv5843594copy number variation1nstd209human GRCh38 chr5: 96,912,314-96,921,835 , GRCh37.p13 chr5: 96,248,018-96,257,539 ERAP1, ERAP2
    nsv5690051mobile element insertion2nstd211human GRCh38 chr5: 96,805,029-96,805,029 , GRCh37.p13 chr5: 96,140,732-96,140,732 ERAP1
    nsv5689338mobile element insertion1nstd211human GRCh38 chr5: 96,856,350-96,856,350 , GRCh37.p13 chr5: 96,192,053-96,192,053 ERAP1
    nsv5684087mobile element insertion2nstd211human GRCh38 chr5: 96,777,532-96,777,532 , GRCh37.p13 chr5: 96,113,236-96,113,236 , ERAP1
    nsv5678136mobile element insertion2nstd211human GRCh38 chr5: 96,808,960-96,808,960 , GRCh37.p13 chr5: 96,144,663-96,144,663 ERAP1
    nsv5678027mobile element insertion1nstd211human GRCh38 chr5: 96,786,120-96,786,120 , GRCh37.p13 chr5: 96,121,824-96,121,824 , ERAP1
    nsv5676601mobile element insertion2nstd211human GRCh38 chr5: 96,899,037-96,899,037 , GRCh37.p13 chr5: 96,234,741-96,234,741 ERAP1, ERAP2
    nsv5641688insertion1nstd207human GRCh38 chr5: 96,896,864-96,896,864 , GRCh37.p13 chr5: 96,232,568-96,232,568 ERAP2, ERAP1
    nsv5635990insertion1nstd207human GRCh38 chr5: 96,805,012-96,805,012 , GRCh37.p13 chr5: 96,140,715-96,140,715 ERAP1
    nsv5579736copy number variation1nstd207human GRCh38 chr5: 96,838,530-96,838,603 , GRCh37.p13 chr5: 96,174,233-96,174,306 ERAP1
    nsv5473710copy number variation1nstd206human GRCh38 chr5: 96,843,561-96,854,386 , GRCh37.p13 chr5: 96,179,264-96,190,089 ERAP1
    nsv5472344copy number variation1nstd206human GRCh38 chr5: 96,895,764-96,895,824 , GRCh37.p13 chr5: 96,231,468-96,231,528 ERAP2, ERAP1
    nsv5470862copy number variation1nstd206human GRCh38 chr5: 96,810,835-96,812,151 , GRCh37.p13 chr5: 96,146,538-96,147,854 ERAP1
    nsv5462035copy number variation1nstd206human GRCh38 chr5: 96,896,864-96,896,965 , GRCh37.p13 chr5: 96,232,568-96,232,669 ERAP2, ERAP1
    nsv5458906copy number variation1nstd206human GRCh38 chr5: 96,911,901-96,922,085 , GRCh37.p13 chr5: 96,247,605-96,257,789 ERAP2, ERAP1
    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