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 465

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974129inversion1nstd209human GRCh38 chr1: 148,280,528-148,303,633 , GRCh37.p13 chr1: 147,752,634-147,775,740 , GRCh37.p13 chr1|NW_003871055.3: 5,095,941-5,119,046 LINC02806, TRH-GTG1-4, 3 more genes
    nsv5887033copy number variation1nstd209human GRCh38 chr1: 148,287,383-148,297,196 , GRCh37.p13 chr1: 147,759,489-147,769,303 , GRCh37.p13 chr1|NW_003871055.3: 5,102,796-5,112,609 LOC105371225, LINC02806
    nsv5885134copy number variation1nstd209human GRCh38 chr1: 143,707,729-148,368,205 , GRCh37.p13 chr1|NW_003871055.3: 523,142-5,183,618 , TRN-GTT22-1, 183 more genes
    nsv5880970copy number variation1nstd209human GRCh38 chr1: 148,298,023-148,298,072 , GRCh37.p13 chr1|NW_003871055.3: 5,113,436-5,113,485 , GRCh37.p13 chr1: 147,770,130-147,770,179 LOC105371225, LINC02806
    nsv5872610copy number variation1nstd209human GRCh38 chr1: 148,286,106-148,286,171 , GRCh37.p13 chr1|NW_003871055.3: 5,101,519-5,101,584 , GRCh37.p13 chr1: 147,758,212-147,758,277 LINC02806
    nsv5828222copy number variation1nstd209human GRCh38 chr1: 148,292,352-148,293,358 , GRCh37.p13 chr1: 147,764,458-147,765,464 , GRCh37.p13 chr1|NW_003871055.3: 5,107,765-5,108,771 LOC105371225, LINC02806
    nsv5828124copy number variation1nstd209human GRCh38 chr1: 148,292,609-148,296,634 , GRCh37.p13 chr1|NW_003871055.3: 5,108,022-5,112,047 , GRCh37.p13 chr1: 147,764,715-147,768,741 LINC02806, LOC105371225
    nsv5828123copy number variation1nstd209human GRCh38 chr1: 148,287,326-148,291,751 , GRCh37.p13 chr1|NW_003871055.3: 5,102,739-5,107,164 , GRCh37.p13 chr1: 147,759,432-147,763,857 LINC02806, LOC105371225
    nsv5674562mobile element insertion1nstd211human GRCh38 chr1: 148,277,955-148,277,955 , GRCh37.p13 chr1|NW_003871055.3: 5,093,368-5,093,368 , GRCh37.p13 chr1: 147,750,073-147,750,073 LINC02806, LINC01731
    nsv5669631inversion1nstd207human GRCh38 chr1: 148,280,433-148,303,584 , GRCh37.p13 chr1: 147,752,539-147,775,691 , GRCh37.p13 chr1|NW_003871055.3: 5,095,846-5,118,997 LINC02806, TRH-GTG1-4, 3 more genes
    nsv5665280inversion1nstd207human GRCh38 chr1: 146,323,908-149,356,055 , GRCh37.p13 chr1|NW_003871055.3: 3,139,321-6,171,468 , BCL9, 98 more genes
    nsv5577207copy number variation1nstd207human GRCh38 chr1: 148,298,023-148,298,072 , GRCh37.p13 chr1|NW_003871055.3: 5,113,436-5,113,485 , GRCh37.p13 chr1: 147,770,130-147,770,179 LOC105371225, LINC02806
    nsv5570249copy number variation1nstd207human GRCh37.p13 chr1|NW_003871055.3: 5,095,462-5,095,520 , GRCh38 chr1: 148,280,049-148,280,107 , GRCh37.p13 chr1: 147,752,155-147,752,213 LINC02806, TRH-GTG1-3, 1 more genes
    nsv5561379sequence alteration1nstd206human GRCh37.p13 chr1|NW_003871055.3: 5,095,670-5,119,135 , GRCh38 chr1: 148,280,257-148,303,722 , GRCh37.p13 chr1: 147,752,363-147,775,829 LINC02806, TRH-GTG1-4, 3 more genes
    nsv5429333copy number variation1nstd206human GRCh38 chr1: 148,092,587-148,533,250 , GRCh37.p13 chr1|NW_003871055.3: 4,908,000-5,348,663 , GRCh37.p13 chr1: 146,034,012-147,581,127 ABHD17AP1, PDE4DIPP1, 31 more genes
    nsv5424475copy number variation1nstd206human GRCh37.p13 chr1|NW_003871055.3: 5,096,482-5,096,930 , GRCh38 chr1: 148,281,069-148,281,517 , GRCh37.p13 chr1: 147,753,175-147,753,623 LINC01731, LINC02806, 1 more genes
    nsv5407638mobile element insertion1nstd206human GRCh38 chr1: 148,277,955-148,278,006 , GRCh37.p13 chr1|NW_003871055.3: 5,093,368-5,093,419 , GRCh37.p13 chr1: 147,750,073-147,750,124 LINC01731, LINC02806
    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
    nsv5370519translocation1nstd200human GRCh38 chr1: 148,296,255-148,296,255 , GRCh38 chr1: 148,294,996-148,294,996 , GRCh37.p13 chr1|NW_003871055.3: 5,110,409-5,110,409 , GRCh37.p13 chr1|NW_003871055.3: 5,111,668-5,111,668 , GRCh37.p13 chr1: 147,767,103-147,767,103 , GRCh37.p13 chr1: 147,768,362-147,768,362 LINC02806, LOC105371225
    nsv5347186translocation1nstd200human GRCh38 chr1: 148,294,655-148,294,655 , GRCh38 chr1: 148,294,576-148,294,576 , GRCh37.p13 chr1|NW_003871055.3: 5,109,989-5,109,989 , GRCh37.p13 chr1: 147,766,683-147,766,683 , GRCh37.p13 chr1|NW_003871055.3: 5,110,068-5,110,068 , GRCh37.p13 chr1: 147,766,762-147,766,762 LOC105371225, LINC02806
    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