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 431

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075909inversion1nstd229human GRCh38 chr13: 77,887,330-77,922,054 , GRCh37.p13 chr13: 78,461,465-78,496,189 EDNRB-AS1, EDNRB
    nsv7065657inversion1nstd229human GRCh38 chr13: 76,225,150-84,243,039 , GRCh37.p13 chr13: 76,799,286-84,817,174 HSPD1P8, ELOCP23, 85 more genes
    nsv7061790inversion1nstd229human GRCh38 chr13: 76,348,646-84,254,120 , GRCh37.p13 chr13: 76,922,782-84,828,255 LINC01068, LOC105370264, 83 more genes
    nsv6957920copy number variation1nstd229human GRCh38 chr13: 77,846,442-77,846,582 , GRCh37.p13 chr13: 78,420,577-78,420,717 EDNRB-AS1
    nsv6957367copy number variation1nstd229human GRCh38 chr13: 77,882,801-77,918,100 , GRCh37.p13 chr13: 78,456,936-78,492,235 EDNRB, EDNRB-AS1
    nsv6956967copy number variation1nstd229human GRCh38 chr13: 77,881,801-77,885,500 , GRCh37.p13 chr13: 78,455,936-78,459,635 EDNRB-AS1
    nsv6956929copy number variation1nstd229human GRCh38 chr13: 77,855,206-77,859,408 , GRCh37.p13 chr13: 78,429,341-78,433,543 EDNRB-AS1
    nsv6956928copy number variation1nstd229human GRCh38 chr13: 77,882,301-77,885,500 , GRCh37.p13 chr13: 78,456,436-78,459,635 EDNRB-AS1
    nsv6956694copy number variation1nstd229human GRCh38 chr13: 77,893,171-77,949,308 , GRCh37.p13 chr13: 78,467,306-78,523,443 RN7SL810P, EDNRB-AS1, 1 more genes
    nsv6955177copy number variation1nstd229human GRCh38 chr13: 77,883,501-77,913,000 , GRCh37.p13 chr13: 78,457,636-78,487,135 EDNRB, EDNRB-AS1
    nsv6955164copy number variation1nstd229human GRCh38 chr13: 77,836,101-77,845,900 , GRCh37.p13 chr13: 78,410,236-78,420,035 EDNRB-AS1
    nsv6954694copy number variation1nstd229human GRCh38 chr13: 77,840,301-77,846,700 , GRCh37.p13 chr13: 78,414,436-78,420,835 EDNRB-AS1
    nsv6953948copy number variation1nstd229human GRCh38 chr13: 77,885,901-77,914,500 , GRCh37.p13 chr13: 78,460,036-78,488,635 EDNRB-AS1, EDNRB
    nsv6953857copy number variation1nstd229human GRCh38 chr13: 77,884,101-77,913,700 , GRCh37.p13 chr13: 78,458,236-78,487,835 EDNRB, EDNRB-AS1
    nsv6953637copy number variation1nstd229human GRCh38 chr13: 77,886,001-77,915,900 , GRCh37.p13 chr13: 78,460,136-78,490,035 EDNRB, EDNRB-AS1
    nsv6953465copy number variation1nstd229human GRCh38 chr13: 77,885,994-77,892,492 , GRCh37.p13 chr13: 78,460,129-78,466,627 EDNRB-AS1
    nsv6952620copy number variation1nstd229human GRCh38 chr13: 77,862,501-77,869,500 , GRCh37.p13 chr13: 78,436,636-78,443,635 EDNRB-AS1
    nsv6952445copy number variation1nstd229human GRCh38 chr13: 77,883,201-77,916,900 , GRCh37.p13 chr13: 78,457,336-78,491,035 EDNRB, EDNRB-AS1
    nsv6951547copy number variation1nstd229human GRCh38 chr13: 77,884,301-77,916,100 , GRCh37.p13 chr13: 78,458,436-78,490,235 EDNRB, EDNRB-AS1
    nsv6949103copy number variation1nstd229human GRCh38 chr13: 77,877,942-77,889,449 , GRCh37.p13 chr13: 78,452,077-78,463,584 EDNRB-AS1
    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