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 141

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5360942translocation1nstd200human GRCh38 chr2: 101,266,879-101,266,879 , GRCh38 chr2: 101,269,038-101,269,038 , GRCh37.p13 chr2: 101,885,500-101,885,500 , GRCh37.p13 chr2: 101,883,341-101,883,341 LOC105373511, CNOT11
    nsv5360941translocation1nstd200human GRCh38 chr2: 101,262,692-101,262,692 , GRCh38 chr2: 101,264,844-101,264,844 , GRCh37.p13 chr2: 101,881,306-101,881,306 , GRCh37.p13 chr2: 101,879,154-101,879,154 LOC105373511, CNOT11
    nsv5281322copy number variation1nstd204human GRCh38.p13 chr2: 100,864,060-101,514,976 , GRCh37.p13 chr2: 101,480,522-102,131,438 LINC01870, LOC105373511, 17 more genes
    nsv5217809copy number variation1nstd204human GRCh38.p13 chr2: 101,225,086-101,251,254 , GRCh37.p13 chr2: 101,841,548-101,867,716 CNOT11
    nsv5217676copy number variation1nstd204human GRCh38.p13 chr2: 100,959,101-101,514,900 , GRCh37.p13 chr2: 101,575,563-102,131,362 RNF149, NPAS2, 17 more genes
    nsv5216147copy number variation1nstd204human GRCh38.p13 chr2: 101,261,265-101,262,592 , GRCh37.p13 chr2: 101,877,727-101,879,054 LOC105373511, CNOT11
    nsv5213131copy number variation1nstd204human GRCh38.p13 chr2: 101,225,986-101,280,641 , GRCh37.p13 chr2: 101,842,448-101,897,103 SNORD89, LOC105373511, 2 more genes
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4894856copy number variation1nstd200human GRCh38 chr2: 100,864,090-101,514,954 , GRCh37.p13 chr2: 101,480,552-102,131,416 CREG2, LOC105373510, 17 more genes
    nsv4786641mobile element deletion1nstd200human GRCh37 chr2: 101,871,675-101,871,965 , GRCh38.p12 chr2: 101,255,213-101,255,503 CNOT11
    nsv4781672copy number variation1nstd200human GRCh37 chr2: 101,480,552-102,131,416 , GRCh38.p12 chr2: 100,864,090-101,514,954 LOC105373512, BBIP1P1, 17 more genes
    nsv4766632inversion1nstd199human GRCh37 chr2: 87,997,505-112,010,501 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,697,986-111,252,924 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 706 more genes
    nsv4752571inversion1nstd199human GRCh37 chr2: 87,550,795-112,295,517 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,323,672-111,537,940 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 723 more genes
    nsv4743379copy number variation1nstd199human GRCh37 chr2: 88,481,090-124,440,189 , GRCh38.p12 chr9: 40,649,751-63,450,622 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 88,181,571-123,682,613 , EIF2AK3, 861 more genes
    nsv4563809mobile element insertion1nstd166human GRCh37.p13 chr2: 101,881,547-101,881,547 , GRCh38.p12 chr2: 101,265,085-101,265,085 CNOT11, LOC105373511
    nsv4519696copy number variation1nstd166human GRCh37.p13 chr2: 101,872,999-101,912,000 , GRCh38.p12 chr2: 101,256,537-101,295,538 RNF149, LOC105373511, 2 more genes
    nsv4518511copy number variation1nstd166human GRCh37.p13 chr2: 101,874,123-101,874,865 , GRCh38.p12 chr2: 101,257,661-101,258,403 LOC105373511, CNOT11
    nsv4462583mobile element insertion1nstd166human GRCh37.p13 chr2: 101,874,209-101,874,209 , GRCh38.p12 chr2: 101,257,747-101,257,747 CNOT11
    nsv4367639copy number variation1nstd173human GRCh37 chr2: 101,838,348-101,868,731 , GRCh38.p12 chr2: 101,221,886-101,252,269 CNOT11
    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