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 190

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978109inversion1nstd209human GRCh38 chr19: 54,222,352-54,696,988 , GRCh37.p13 chr19|NW_004166865.1: 196,719-671,355 LAIR1, LAIR2, 29 more genes
    nsv5562753sequence alteration1nstd206human GRCh38 chr19: 54,280,539-54,594,201 , GRCh37.p13 chr19|NW_004166865.1: 254,906-568,568 LAIR1, LILRB2, 16 more genes
    nsv5529187copy number variation1nstd206human GRCh38 chr19: 54,339,463-54,345,126 , GRCh37.p13 chr19|NW_004166865.1: 313,830-319,493 LILRA4
    nsv5528992copy number variation1nstd206human GRCh38 chr19: 54,335,786-54,368,019 , GRCh37.p13 chr19|NW_004166865.1: 310,153-342,386 LAIR1, LILRA4
    nsv5521652copy number variation1nstd206human GRCh38 chr19: 54,339,414-54,340,460 , GRCh37.p13 chr19|NW_004166865.1: 313,781-314,827 LILRA4
    nsv5521170copy number variation1nstd206human GRCh38 chr19: 54,220,538-54,336,889 , GRCh37.p13 chr19|NW_004166865.1: 194,905-311,256 LILRA4, MIR4752, 10 more genes
    nsv5520408copy number variation1nstd206human GRCh38 chr19: 54,339,243-54,339,831 , GRCh37.p13 chr19|NW_004166865.1: 313,610-314,198 LILRA4
    nsv5514181copy number variation1nstd206human GRCh38 chr19: 54,339,435-54,340,565 , GRCh37.p13 chr19|NW_004166865.1: 313,802-314,932 LILRA4
    nsv5325400copy number variation1nstd204human GRCh38.p13 chr19: 54,339,277-54,339,840 , GRCh37.p13 chr19|NW_004166865.1: 313,644-314,207 LILRA4
    nsv5324812copy number variation1nstd204human GRCh38.p13 chr19: 54,220,162-54,337,386 , GRCh37.p13 chr19|NW_004166865.1: 194,529-311,753 LOC100421130, LILRA6, 10 more genes
    nsv5322642copy number variation1nstd204human GRCh38.p13 chr19: 54,319,172-54,335,924 , GRCh37.p13 chr19|NW_004166865.1: 293,539-310,291 VN1R104P, LILRA4
    nsv5294579copy number variation1nstd204human GRCh38.p13 chr19: 54,319,850-54,334,539 , GRCh37.p13 chr19|NW_004166865.1: 294,217-308,906 LILRA4, VN1R104P
    nsv5289362copy number variation1nstd204human GRCh37.p13 chr19|NW_004166865.1: 255,468-388,067 , GRCh38.p13 chr19: 54,281,101-54,413,700 LAIR1, LILRB2, 5 more genes
    nsv5288289copy number variation1nstd204human GRCh38.p13 chr19: 54,240,801-54,349,500 , GRCh37.p13 chr19|NW_004166865.1: 215,168-323,867 RNU6-1307P, LOC100420187, 8 more genes
    nsv5285190copy number variation1nstd204human GRCh38.p13 chr19: 54,333,565-54,335,756 , GRCh37.p13 chr19|NW_004166865.1: 307,932-310,123 LILRA4
    nsv5024927copy number variation1nstd200human GRCh38 chr19: 54,319,398-54,335,748 , GRCh37.p13 chr19|NW_004166865.1: 293,765-310,115 LILRA4, VN1R104P
    nsv5024926copy number variation1nstd200human GRCh38 chr19: 54,275,041-54,433,399 , GRCh37.p13 chr19|NW_004166865.1: 249,408-407,766 LAIR1, LILRA5, 5 more genes
    nsv4865322copy number variation1nstd200human GRCh37 chr19: 54,830,673-54,847,016 , GRCh38.p12 chr19|NW_003571061.2: 300,901-317,246 , GRCh38.p12 chr19|NW_003571055.2: 300,747-317,092 , GRCh38.p12 chr19: 54,319,401-54,335,745 , GRCh38.p12 chr19|NT_187693.1: 301,787-318,130 , GRCh38.p12 chr19|NW_003571054.1: 300,818-309,799 LILRA4, VN1R104P
    nsv4861346copy number variation1nstd200human GRCh37 chr19: 54,836,186-55,143,468 , GRCh38.p12 chr19|NT_187693.1: 307,300-614,582 , GRCh38.p12 chr19|NW_003571060.1: 258,364-536,895 , GRCh38.p12 chr19|NW_003571054.1: 306,331-538,403 , GRCh38.p12 chr19: 54,324,914-54,632,017 LAIR2, LILRA4, 14 more genes
    nsv4853592copy number variation1nstd200human GRCh37 chr19: 54,850,589-54,851,111 , GRCh38.p12 chr19: 54,339,318-54,339,841 , GRCh38.p12 chr19|NW_003571061.2: 320,819-321,341 , GRCh38.p12 chr19|NW_003571055.2: 320,665-321,187 , GRCh38.p12 chr19|NT_187693.1: 321,703-322,225 LILRA4
    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