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 278

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5889687copy number variation1nstd209human GRCh38 chr4: 174,265,236-174,265,297 , GRCh37.p13 chr4: 175,186,387-175,186,448 FBXO8
    nsv5838146copy number variation1nstd209human GRCh38 chr4: 174,257,211-174,276,857 , GRCh37.p13 chr4: 175,178,362-175,198,008 FBXO8
    nsv5677952mobile element insertion2nstd211human GRCh38 chr4: 174,273,331-174,273,331 , GRCh37.p13 chr4: 175,194,482-175,194,482 FBXO8
    nsv5635147insertion1nstd207human GRCh38 chr4: 174,273,323-174,273,323 , GRCh37.p13 chr4: 175,194,474-175,194,474 FBXO8
    nsv5567021copy number variation1nstd207human GRCh38 chr4: 174,265,236-174,265,297 , GRCh37.p13 chr4: 175,186,387-175,186,448 FBXO8
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5397386mobile element insertion1nstd206human GRCh38 chr4: 174,273,331-174,273,331 , GRCh37.p13 chr4: 175,194,482-175,194,482 FBXO8
    nsv5180321mobile element insertion1nstd203human GRCh38 chr4: 174,241,049-174,241,060 , GRCh37.p13 chr4: 175,162,200-175,162,211 FBXO8
    nsv5098121mobile element insertion1nstd203human GRCh38 chr4: 174,273,316-174,273,331 , GRCh37.p13 chr4: 175,194,467-175,194,482 FBXO8
    nsv5097256mobile element insertion1nstd203human GRCh38 chr4: 174,256,536-174,256,548 , GRCh37.p13 chr4: 175,177,687-175,177,699 FBXO8
    nsv5092293mobile element insertion1nstd203human GRCh38 chr4: 174,273,321-174,273,331 , GRCh37.p13 chr4: 175,194,472-175,194,482 FBXO8
    nsv5091885mobile element insertion1nstd203human GRCh38 chr4: 174,273,330-174,273,330 , GRCh37.p13 chr4: 175,194,481-175,194,481 FBXO8
    nsv5086486mobile element insertion1nstd203human GRCh38 chr4: 174,273,329-174,273,331 , GRCh37.p13 chr4: 175,194,480-175,194,482 FBXO8
    nsv5085938mobile element insertion1nstd203human GRCh38 chr4: 174,273,314-174,273,331 , GRCh37.p13 chr4: 175,194,465-175,194,482 FBXO8
    nsv5085481mobile element insertion1nstd203human GRCh38 chr4: 174,273,313-174,273,331 , GRCh37.p13 chr4: 175,194,464-175,194,482 FBXO8
    nsv5083475mobile element insertion1nstd203human GRCh38 chr4: 174,273,323-174,273,331 , GRCh37.p13 chr4: 175,194,474-175,194,482 FBXO8
    nsv5082820mobile element insertion1nstd203human GRCh38 chr4: 174,273,312-174,273,331 , GRCh37.p13 chr4: 175,194,463-175,194,482 FBXO8
    nsv5081869mobile element insertion1nstd203human GRCh38 chr4: 174,273,322-174,273,331 , GRCh37.p13 chr4: 175,194,473-175,194,482 FBXO8
    nsv4944062copy number variation1nstd200human GRCh38 chr4: 173,724,041-174,933,391 , GRCh37.p13 chr4: 174,645,192-175,854,542 LOC107986204, LOC101928551, 16 more genes
    nsv4934275copy number variation1nstd200human GRCh38 chr4: 174,240,106-174,267,709 , GRCh37.p13 chr4: 175,161,257-175,188,860 FBXO8
    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