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 785

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129440mobile element insertion1nstd186human GRCh37 chr17: 58,475,336-58,475,350 , GRCh38.p12 chr17: 60,397,975-60,397,989 USP32
    nsv6128784copy number variation1nstd186human GRCh37 chr17: 58,411,782-58,414,077 , GRCh38.p12 chr17: 60,334,421-60,336,716 USP32
    nsv6127307copy number variation1nstd186human GRCh37 chr17: 58,446,360-58,446,654 , GRCh38.p12 chr17: 60,368,999-60,369,293 USP32
    nsv5944768copy number variation1nstd209human GRCh38 chr17: 60,334,536-60,336,559 , GRCh37.p13 chr17: 58,411,897-58,413,920 USP32
    nsv5942830copy number variation1nstd209human GRCh38 chr17: 60,313,181-60,313,230 , GRCh37.p13 chr17: 58,390,542-58,390,591 USP32
    nsv5940299copy number variation1nstd209human GRCh38 chr17: 60,249,856-60,249,923 , GRCh37.p13 chr17: 58,327,217-58,327,284 USP32
    nsv5937711copy number variation1nstd209human GRCh38 chr17: 60,298,088-60,298,140 , GRCh37.p13 chr17: 58,375,449-58,375,501 USP32
    nsv5936071copy number variation1nstd209human GRCh38 chr17: 60,389,387-60,389,860 , GRCh37.p13 chr17: 58,466,748-58,467,221 USP32
    nsv5932410copy number variation1nstd209human GRCh38 chr17: 60,411,409-60,411,638 , GRCh37.p13 chr17: 58,488,770-58,488,999 USP32, LOC105371850
    nsv5877628copy number variation1nstd209human GRCh38 chr17: 60,334,635-60,336,434 , GRCh37.p13 chr17: 58,411,996-58,413,795 USP32
    nsv5870004copy number variation1nstd209human GRCh38 chr17: 60,275,263-60,276,362 , GRCh37.p13 chr17: 58,352,624-58,353,723 USP32
    nsv5729571mobile element insertion1nstd211human GRCh38 chr17: 60,393,038-60,393,038 , GRCh37.p13 chr17: 58,470,399-58,470,399 USP32
    nsv5725297mobile element insertion2nstd211human GRCh38 chr17: 60,289,939-60,289,939 , GRCh37.p13 chr17: 58,367,300-58,367,300 USP32
    nsv5723950mobile element insertion1nstd211human GRCh38 chr17: 60,344,146-60,344,146 , GRCh37.p13 chr17: 58,421,507-58,421,507 USP32
    nsv5718445mobile element insertion2nstd211human GRCh38 chr17: 60,414,608-60,414,608 , GRCh37.p13 chr17: 58,491,969-58,491,969 USP32, LOC105371850
    nsv5715202mobile element insertion2nstd211human GRCh38 chr17: 60,397,975-60,397,975 , GRCh37.p13 chr17: 58,475,336-58,475,336 USP32
    nsv5710510mobile element insertion1nstd211human GRCh38 chr17: 60,190,541-60,190,541 , GRCh37.p13 chr17: 58,267,902-58,267,902 USP32
    nsv5710457mobile element insertion1nstd211human GRCh38 chr17: 60,286,724-60,286,724 , GRCh37.p13 chr17: 58,364,085-58,364,085 USP32
    nsv5710306mobile element insertion2nstd211human GRCh38 chr17: 60,401,552-60,401,552 , GRCh37.p13 chr17: 58,478,913-58,478,913 LOC105371850, USP32
    nsv5707666mobile element insertion2nstd211human GRCh38 chr17: 60,412,009-60,412,009 , GRCh37.p13 chr17: 58,489,370-58,489,370 LOC105371850, USP32
    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