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 212

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5684983mobile element insertion1nstd211human GRCh38 chr2: 138,528,736-138,528,736 , GRCh37.p13 chr2: 139,286,306-139,286,306 SPOPL
    nsv5675992mobile element insertion1nstd211human GRCh38 chr2: 138,504,986-138,504,986 , GRCh37.p13 chr2: 139,262,556-139,262,556 SPOPL
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5450202copy number variation1nstd206human GRCh38 chr2: 138,533,543-138,533,632 , GRCh37.p13 chr2: 139,291,113-139,291,202 SPOPL
    nsv5401863mobile element insertion1nstd206human GRCh38 chr2: 138,528,736-138,528,787 , GRCh37.p13 chr2: 139,286,306-139,286,357 SPOPL
    nsv5400848mobile element insertion1nstd206human GRCh38 chr2: 138,504,986-138,505,037 , GRCh37.p13 chr2: 139,262,556-139,262,607 SPOPL
    nsv5381338copy number variation1nstd102humanPathogenic GRCh37 chr2: 136,473,383-152,727,396 , GRCh38.p12 chr2: 135,715,813-151,870,882 YY1P2, SPOPL, 156 more genes
    nsv5366500translocation1nstd200human GRCh38 chr2: 138,559,931-138,559,931 , GRCh38 chr7: 11,666,484-11,666,484 , GRCh37.p13 chr2: 139,317,501-139,317,501 , GRCh37.p13 chr7: 11,706,111-11,706,111 THSD7A, SPOPL
    nsv5350790translocation1nstd200human GRCh38 chr2: 138,533,632-138,533,632 , GRCh38 chr2: 138,533,543-138,533,543 , GRCh37.p13 chr2: 139,291,202-139,291,202 , GRCh37.p13 chr2: 139,291,113-139,291,113 SPOPL
    nsv5350789translocation1nstd200human GRCh38 chr2: 138,522,732-138,522,732 , GRCh38 chr2: 138,522,672-138,522,672 , GRCh37.p13 chr2: 139,280,242-139,280,242 , GRCh37.p13 chr2: 139,280,302-139,280,302 SPOPL
    nsv5345301translocation1nstd200human GRCh37 chr2: 139,317,501-139,317,501 , GRCh37 chr7: 11,706,111-11,706,111 , GRCh38.p12 chr2: 138,559,931-138,559,931 , GRCh38.p12 chr7: 11,666,484-11,666,484 THSD7A, SPOPL
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4909537copy number variation1nstd200human GRCh38 chr2: 138,545,726-138,547,219 , GRCh37.p13 chr2: 139,303,296-139,304,789 SPOPL
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4771078copy number variation1nstd200human GRCh37 chr2: 139,303,296-139,304,789 , GRCh38.p12 chr2: 138,545,726-138,547,219 SPOPL
    nsv4771077copy number variation1nstd200human GRCh37 chr2: 139,297,951-139,299,021 , GRCh38.p12 chr2: 138,540,381-138,541,451 SPOPL
    nsv4771076copy number variation1nstd200human GRCh37 chr2: 139,291,113-139,291,202 , GRCh38.p12 chr2: 138,533,543-138,533,632 SPOPL
    nsv4771026copy number variation1nstd200human GRCh37 chr2: 137,223,576-141,429,363 , GRCh38.p12 chr2: 136,466,006-140,671,794 LRP1B, LOC101928273, 35 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