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 185

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977675insertion1nstd209human GRCh38 chr15: 74,894,107-74,894,107 , GRCh37.p13 chr15: 75,186,448-75,186,448 MPI
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5672749copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 75,188,483-75,190,081 , GRCh38.p12 chr15: 74,896,142-74,897,740 MPI, FAM219B
    nsv5661680insertion1nstd207human GRCh38 chr15: 74,894,107-74,894,107 , GRCh37.p13 chr15: 75,186,448-75,186,448 MPI
    nsv5650594insertion1nstd207human GRCh38 chr15: 74,894,043-74,894,043 , GRCh37.p13 chr15: 75,186,384-75,186,384 MPI
    nsv5390426copy number variation2nstd186human GRCh37 chr15: 75,186,341-75,186,538 , GRCh38.p12 chr15: 74,894,000-74,894,197 MPI
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5320176copy number variation1nstd204human GRCh38.p13 chr15: 74,893,975-74,894,222 , GRCh37.p13 chr15: 75,186,316-75,186,563 MPI
    nsv5265043copy number variation1nstd204human GRCh38.p13 chr15: 74,898,313-74,899,762 , GRCh37.p13 chr15: 75,190,654-75,192,103 MPI, FAM219B
    nsv5264751copy number variation1nstd204human GRCh38.p13 chr15: 74,898,763-74,899,762 , GRCh37.p13 chr15: 75,191,104-75,192,103 MPI, FAM219B
    nsv5009060copy number variation1nstd200human GRCh38 chr15: 74,894,000-74,894,197 , GRCh37.p13 chr15: 75,186,341-75,186,538 MPI
    nsv5009059copy number variation1nstd200human GRCh38 chr15: 74,879,952-74,892,281 , GRCh37.p13 chr15: 75,172,293-75,184,622 MPI
    nsv5009057copy number variation1nstd200human GRCh38 chr15: 74,796,648-74,914,092 , GRCh37.p13 chr15: 75,088,989-75,206,433 CSK, SCAMP2, 7 more genes
    nsv5001758copy number variation1nstd200human GRCh38 chr15: 74,901,740-74,902,867 , GRCh37.p13 chr15: 75,194,081-75,195,208 FAM219B, MPI
    nsv4992298copy number variation1nstd200human GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519 , SNUPN, 215 more genes
    nsv4863885copy number variation1nstd200human GRCh37 chr15: 75,186,341-75,186,538 , GRCh38.p12 chr15: 74,894,000-74,894,197 MPI
    nsv4863884copy number variation1nstd200human GRCh37 chr15: 75,172,292-75,184,623 , GRCh38.p12 chr15: 74,879,951-74,892,282 MPI
    nsv4850102copy number variation1nstd200human GRCh37 chr15: 75,186,567-75,187,380 , GRCh38.p12 chr15: 74,894,226-74,895,039 MPI
    nsv4756988insertion1nstd199human GRCh37 chr15: 75,186,476-75,186,476 , GRCh38.p12 chr15: 74,894,135-74,894,135 MPI
    nsv4729106copy number variation1nstd102humanPathogenic GRCh37 chr15: 74,398,162-76,054,094 , GRCh38.p12 chr15: 74,105,821-75,761,753 FAM219B, MIR4513, 62 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