U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 859

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5036917mobile element deletion1nstd200human GRCh38 chr5: 78,251,671-78,258,846 , GRCh37.p13 chr5: 77,547,495-77,554,670 AP3B1
    nsv4878710mobile element deletion1nstd200human GRCh37 chr5: 77,547,478-77,554,685 , GRCh38.p12 chr5: 78,251,654-78,258,861 AP3B1
    nsv5031500mobile element deletion1nstd200human GRCh38 chr3: 54,467,626-54,474,424 , GRCh37.p13 chr3: 54,501,653-54,508,451 CACNA2D3
    nsv4886286mobile element deletion1nstd200human GRCh37 chr12: 127,579,247-127,585,813 , GRCh38.p12 chr12|NW_019805499.1: 41,226-47,792 , GRCh38.p12 chr12: 127,094,702-127,101,268 LOC107984449
    nsv5032617mobile element deletion1nstd200human GRCh38 chr12: 127,094,649-127,101,307 , GRCh37.p13 chr12: 127,579,194-127,585,852 LOC107984449
    nsv4885539mobile element deletion1nstd200human GRCh37 chr14: 86,562,024-86,568,475 , GRCh38.p12 chr14: 86,095,680-86,102,131 LINC02328
    nsv5041038mobile element deletion1nstd200human GRCh38 chr12: 129,800,153-129,806,571 , GRCh37.p13 chr12: 130,284,698-130,291,116 TMEM132D
    nsv5033290mobile element deletion1nstd200human GRCh38 chr8: 123,859,652-123,866,014 , GRCh37.p13 chr8: 124,871,892-124,878,254 FER1L6
    nsv4872633mobile element deletion1nstd200human GRCh37 chr11: 21,690,376-21,696,762 , GRCh38.p12 chr11: 21,668,830-21,675,216
    nsv5035171mobile element deletion1nstd200human GRCh38 chr11: 21,668,833-21,675,201 , GRCh37.p13 chr11: 21,690,379-21,696,747
    nsv5032101mobile element deletion1nstd200human GRCh38 chr12: 106,465,886-106,472,257 , GRCh37.p13 chr12: 106,859,664-106,866,035 POLR3B
    nsv5035263mobile element deletion1nstd200human GRCh38 chr13: 74,426,103-74,432,368 , GRCh37.p13 chr13: 75,000,240-75,006,505 LINC00381
    nsv4879705mobile element deletion1nstd200human GRCh37 chr13: 75,000,240-75,006,505 , GRCh38.p12 chr13: 74,426,103-74,432,368 LINC00381
    nsv5038197mobile element deletion1nstd200human GRCh38 chr2: 166,988,451-166,994,698 , GRCh37.p13 chr2: 167,844,961-167,851,208 XIRP2
    nsv4880831mobile element deletion1nstd200human GRCh37 chr2: 167,844,961-167,851,208 , GRCh38.p12 chr2: 166,988,451-166,994,698 XIRP2
    nsv5034655mobile element deletion1nstd200human GRCh38 chr5: 13,416,495-13,422,741 , GRCh37.p13 chr5: 13,416,607-13,422,853 LOC105374660
    nsv4878135mobile element deletion1nstd200human GRCh37 chr5: 13,416,607-13,422,853 , GRCh38.p12 chr5: 13,416,495-13,422,741 LOC105374660
    nsv5031363mobile element deletion1nstd200human GRCh38 chrX: 11,935,080-11,941,316 , GRCh37.p13 chrX: 11,953,199-11,959,435 FRMPD4
    nsv4878989mobile element deletion1nstd200human GRCh37 chrX: 11,953,199-11,959,435 , GRCh38.p12 chrX: 11,935,080-11,941,316 FRMPD4
    nsv5036275mobile element deletion1nstd200human GRCh38 chr6: 19,764,871-19,771,123 , GRCh37.p13 chr6: 19,765,102-19,771,354 LNC-LBCS
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center