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 606

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112770copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,616,095-28,538,904 , GRCh38.p12 chr15: 23,370,948-28,293,758 LOC105370728, SNORD115-14, 144 more genes
    nsv5944381copy number variation1nstd209human GRCh38 chr15: 25,227,144-25,232,421 , GRCh37.p13 chr15: 25,472,291-25,477,568 SNORD115-31, SNORD115-32, 4 more genes
    nsv5933803copy number variation1nstd209human GRCh38 chr15: 25,215,887-25,227,452 , GRCh37.p13 chr15: 25,461,034-25,472,599 SNORD115-25, SNORD115-26, 7 more genes
    nsv5860513copy number variation1nstd209human GRCh38 chr15: 25,227,126-25,232,425 , GRCh37.p13 chr15: 25,472,273-25,477,572 SNORD115-31, SNORD115-32, 4 more genes
    nsv5672660copy number variation1nstd102humanPathogenic GRCh38 chr15: 22,804,175-30,375,696 , GRCh37.p13 chr15: 23,564,855-30,667,899 TUBBP8, LOC102723564, 218 more genes
    nsv5665288inversion1nstd207human GRCh38 chr15: 25,228,118-25,252,402 , GRCh37.p13 chr15: 25,473,265-25,497,549 SNORD115-32, SNORD115-33, 12 more genes
    nsv5588877copy number variation1nstd207human GRCh38 chr15: 25,223,453-25,227,312 , GRCh37.p13 chr15: 25,468,600-25,472,459 SNORD115-29, SNORD115-30, 3 more genes
    nsv5587366copy number variation1nstd207human GRCh38 chr15: 25,227,587-25,228,408 , GRCh37.p13 chr15: 25,472,734-25,473,555 SNORD115-31, SNORD115-32, 1 more genes
    nsv5563124sequence alteration1nstd206human GRCh38 chr15: 25,227,420-25,227,444 , GRCh37.p13 chr15: 25,472,567-25,472,591 SNORD115-31, SNORD115-32, 1 more genes
    nsv5557813sequence alteration1nstd206human GRCh38 chr15: 23,786,776-25,754,615 , GRCh37.p13 chr15: 24,031,923-25,999,762 , IPW, 110 more genes
    nsv5390973copy number variation1nstd186human GRCh37 chr15: 25,472,364-25,477,533 , GRCh38.p12 chr15: 25,227,217-25,232,386 SNORD115-31, SNORD115-32, 4 more genes
    nsv5390534copy number variation1nstd186human GRCh37 chr15: 25,472,364-25,477,529 , GRCh38.p12 chr15: 25,227,217-25,232,382 SNORD115-31, SNORD115-32, 4 more genes
    nsv5381773copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,525-27,193,380 , GRCh38.p12 chr15: 23,319,714-26,948,233 SNORD116-5, NPAP1, 139 more genes
    nsv5309348copy number variation1nstd204human GRCh38.p13 chr15: 25,215,462-25,239,821 , GRCh37.p13 chr15: 25,460,609-25,484,968 SNORD115-35, SNORD115-38, 14 more genes
    nsv5279003copy number variation1nstd204human GRCh38.p13 chr15: 25,226,926-25,228,625 , GRCh37.p13 chr15: 25,472,073-25,473,772 SNHG14, SNORD115-31, 1 more genes
    nsv5275540copy number variation1nstd204human GRCh38.p13 chr15: 25,227,526-25,232,225 , GRCh37.p13 chr15: 25,472,673-25,477,372 SNORD115-32, SNORD115-31, 3 more genes
    nsv5200367copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,208,842-28,525,460 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,280,314 SNORD115-27, LOC105370747, 246 more genes
    nsv5148517mobile element insertion1nstd203human GRCh38 chr15: 25,229,014-25,229,029 , GRCh37.p13 chr15: 25,474,161-25,474,176 SNORD115-32, SNORD115-33, 1 more genes
    nsv5060035copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,707,435-28,726,651 , GRCh38.p12 chr15: 23,462,288-28,481,505 PWAR4, SNORD116-18, 150 more genes
    nsv5000941copy number variation1nstd200human GRCh38 chr15: 25,228,674-25,232,809 , GRCh37.p13 chr15: 25,473,821-25,477,956 SNORD115-34, SNORD115-35, 3 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