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 404

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979346insertion1nstd209human GRCh38 chr15: 50,495,295-50,495,295 , GRCh37.p13 chr15: 50,787,492-50,787,492 , USP8
    nsv5939682copy number variation1nstd209human GRCh38 chr15: 50,468,133-50,470,029 , GRCh37.p13 chr15: 50,760,330-50,762,226 USP8
    nsv5937046copy number variation1nstd209human GRCh38 chr15: 50,506,960-50,508,068 , GRCh37.p13 chr15: 50,799,157-50,800,265 USP50, USP8
    nsv5936365copy number variation1nstd209human GRCh38 chr15: 50,511,312-50,513,241 , GRCh37.p13 chr15: 50,803,509-50,805,438 USP8, USP50
    nsv5930039copy number variation1nstd209human GRCh38 chr15: 50,476,256-50,892,576 , GRCh37.p13 chr15: 50,768,453-51,184,773 , USP8, 5 more genes
    nsv5929801copy number variation1nstd209human GRCh38 chr15: 50,454,975-50,455,467 , GRCh37.p13 chr15: 50,747,172-50,747,664 USP8
    nsv5865273copy number variation1nstd209human GRCh38 chr15: 50,513,091-50,517,627 , GRCh37.p13 chr15: 50,805,288-50,809,824 USP8, USP50
    nsv5862535copy number variation1nstd209human GRCh38 chr15: 50,468,124-50,470,123 , GRCh37.p13 chr15: 50,760,321-50,762,320 USP8
    nsv5856408copy number variation1nstd209human GRCh38 chr15: 50,476,236-50,487,583 , GRCh37.p13 chr15: 50,768,433-50,779,780 USP8
    nsv5849631copy number variation2nstd209human GRCh38 chr15: 50,511,191-50,513,390 , GRCh37.p13 chr15: 50,803,388-50,805,587 USP50, USP8
    nsv5697893mobile element insertion1nstd211human GRCh38 chr15: 50,500,106-50,500,106 , GRCh37.p13 chr15: 50,792,303-50,792,303 USP8, USP50
    nsv5695201mobile element insertion1nstd211human GRCh38 chr15: 50,485,583-50,485,583 , GRCh37.p13 chr15: 50,777,780-50,777,780 USP8
    nsv5694641mobile element insertion1nstd211human GRCh38 chr15: 50,478,441-50,478,441 , GRCh37.p13 chr15: 50,770,638-50,770,638 USP8
    nsv5655298insertion1nstd207human GRCh38 chr15: 50,509,297-50,509,297 , GRCh37.p13 chr15: 50,801,494-50,801,494 USP50, USP8
    nsv5646998insertion1nstd207human GRCh38 chr15: 50,499,178-50,499,178 , GRCh37.p13 chr15: 50,791,375-50,791,375 USP8, USP50
    nsv5588468copy number variation1nstd207human GRCh38 chr15: 50,495,239-50,495,294 , GRCh37.p13 chr15: 50,787,436-50,787,491 , USP8
    nsv5587204copy number variation1nstd207human GRCh38 chr15: 50,454,975-50,455,467 , GRCh37.p13 chr15: 50,747,172-50,747,664 USP8
    nsv5564218copy number variation1nstd102humanUncertain significance GRCh37 chr15: 50,731,261-50,791,295 , GRCh38.p12 chr15: 50,439,064-50,499,098 USP8, RNA5SP395, 2 more genes
    nsv5531113copy number variation1nstd206human GRCh38 chr15: 50,501,270-50,504,716 , GRCh37.p13 chr15: 50,793,467-50,796,913 USP50, USP8
    nsv5529412copy number variation1nstd206human GRCh38 chr15: 50,454,976-50,455,468 , GRCh37.p13 chr15: 50,747,173-50,747,665 USP8
    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