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 317

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130115mobile element insertion1nstd186human GRCh37 chr17: 17,995,477-17,995,526 , GRCh38.p12 chr17: 18,092,163-18,092,212 DRG2
    nsv5975286insertion1nstd209human GRCh38 chr17: 18,092,147-18,092,147 , GRCh37.p13 chr17: 17,995,461-17,995,461 DRG2
    nsv5974534inversion1nstd209human GRCh38 chr17: 15,750,079-18,634,890 , GRCh37.p13 chr17: 15,653,393-18,538,203 , ADORA2B, 119 more genes
    nsv5933579copy number variation1nstd209human GRCh38 chr17: 16,936,959-20,558,118 , GRCh37.p13 chr17: 16,840,273-20,461,431 , FAM106B, 146 more genes
    nsv5727094mobile element insertion2nstd211human GRCh38 chr17: 18,092,163-18,092,163 , GRCh37.p13 chr17: 17,995,477-17,995,477 DRG2
    nsv5665112inversion1nstd207human GRCh37.p13 chr17: 16,704,599-18,417,421 , GRCh38 chr17: 16,801,285-18,514,107 , DRG2, 71 more genes
    nsv5656817insertion1nstd207human GRCh38 chr17: 18,092,147-18,092,147 , GRCh37.p13 chr17: 17,995,461-17,995,461 DRG2
    nsv5590224copy number variation1nstd207human GRCh38 chr17: 18,090,679-18,090,814 , GRCh37.p13 chr17: 17,993,993-17,994,128 DRG2
    nsv5556223mobile element insertion1nstd206human GRCh38 chr17: 18,092,163-18,092,212 , GRCh37.p13 chr17: 17,995,477-17,995,526 DRG2
    nsv5517349copy number variation1nstd206human GRCh38 chr17: 18,090,590-18,093,508 , GRCh37.p13 chr17: 17,993,904-17,996,822 DRG2
    nsv5514735copy number variation1nstd206human GRCh38 chr17: 18,089,310-18,093,525 , GRCh37.p13 chr17: 17,992,624-17,996,839 DRG2
    nsv5381800copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,601,603-20,063,369 , GRCh38.p12 chr17: 16,698,289-20,160,056 COTL1P1, LOC105371551, 141 more genes
    nsv5381797copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,145,361-20,137,943 , GRCh38.p12 chr17: 17,242,047-20,234,630 LOC644909, FLII, 117 more genes
    nsv5316176copy number variation1nstd204human GRCh38.p13 chr17: 18,089,409-18,093,534 , GRCh37.p13 chr17: 17,992,723-17,996,848 DRG2
    nsv5297671copy number variation1nstd204human GRCh38.p13 chr17: 18,089,401-18,095,000 , GRCh37.p13 chr17: 17,992,715-17,998,314 DRG2
    nsv5294002copy number variation1nstd204human GRCh38.p13 chr17: 18,092,112-18,093,449 , GRCh37.p13 chr17: 17,995,426-17,996,763 DRG2
    nsv5280936copy number variation1nstd204human GRCh38.p13 chr17: 17,763,701-18,133,000 , GRCh37.p13 chr17: 17,667,015-18,036,314 GID4, MIR33B, 14 more genes
    nsv5199636mobile element insertion1nstd203human GRCh38 chr17: 18,092,147-18,092,163 , GRCh37.p13 chr17: 17,995,461-17,995,477 DRG2
    nsv5185216mobile element insertion1nstd203human GRCh38 chr17: 18,092,152-18,092,160 , GRCh37.p13 chr17: 17,995,466-17,995,474 DRG2
    nsv5026144copy number variation1nstd200human GRCh38 chr17: 18,108,043-18,110,575 , GRCh37.p13 chr17: 18,011,357-18,013,889 LOC105371566, DRG2, 1 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