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 188

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5956071insertion1nstd209human GRCh38 chr1: 151,367,355-151,367,355 , GRCh37.p13 chr1: 151,339,831-151,339,831 SELENBP1
    nsv5886646copy number variation1nstd209human GRCh38 chr1: 151,359,619-151,435,986 , GRCh37.p13 chr1: 151,332,095-151,408,462 PSMB4, SELENBP1, 1 more genes
    nsv5828135copy number variation1nstd209human GRCh38 chr1: 151,358,773-151,366,909 , GRCh37.p13 chr1: 151,331,249-151,339,385 SELENBP1
    nsv5541942insertion1nstd206human GRCh38 chr1: 151,371,425-151,371,462 , GRCh37.p13 chr1: 151,343,901-151,343,938 SELENBP1
    nsv5422762copy number variation1nstd206human GRCh38 chr1: 151,370,191-151,387,707 , GRCh37.p13 chr1: 151,342,667-151,360,183 SELENBP1
    nsv5415260copy number variation1nstd206human GRCh38 chr1: 151,366,977-151,367,054 , GRCh37.p13 chr1: 151,339,453-151,339,530 SELENBP1
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5381206copy number variation1nstd102humanUncertain significance GRCh37 chr1: 151,122,490-151,585,008 , GRCh38.p12 chr1: 151,150,014-151,612,532 CGN, ZNF687-AS1, 21 more genes
    nsv5219564copy number variation1nstd204human GRCh38.p13 chr1: 151,301,601-151,394,300 , GRCh37.p13 chr1: 151,274,077-151,366,776 RFX5, RFX5-AS1, 2 more genes
    nsv5079261mobile element insertion1nstd203human GRCh38 chr1: 151,371,416-151,371,425 , GRCh37.p13 chr1: 151,343,892-151,343,901 SELENBP1
    nsv5064216mobile element insertion1nstd203human GRCh38 chr1: 151,371,411-151,371,425 , GRCh37.p13 chr1: 151,343,887-151,343,901 SELENBP1
    nsv4897378copy number variation1nstd200human GRCh38 chr1: 151,358,372-151,389,526 , GRCh37.p13 chr1: 151,330,848-151,362,002 SELENBP1
    nsv4894675copy number variation1nstd200human GRCh38 chr1: 151,370,191-151,387,707 , GRCh37.p13 chr1: 151,342,667-151,360,183 SELENBP1
    nsv4894674copy number variation1nstd200human GRCh38 chr1: 151,356,470-151,369,446 , GRCh37.p13 chr1: 151,328,946-151,341,922 SELENBP1
    nsv4784214copy number variation1nstd200human GRCh37 chr1: 151,330,848-151,362,002 , GRCh38.p12 chr1: 151,358,372-151,389,526 SELENBP1
    nsv4781185copy number variation1nstd200human GRCh37 chr1: 151,342,667-151,360,183 , GRCh38.p12 chr1: 151,370,191-151,387,707 SELENBP1
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4712598copy number variation1nstd195human GRCh37 chr1: 151,042,151-151,571,701 , GRCh38.p12 chr1: 151,069,675-151,599,225 PI4KB, PSMD4, 24 more genes
    nsv4645167copy number variation1nstd186human GRCh37 chr1: 151,333,216-151,413,627 , GRCh38.p12 chr1: 151,360,740-151,441,151 PSMB4, SELENBP1, 2 more genes
    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