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 279

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935094copy number variation1nstd209human GRCh38 chr17: 28,172,152-28,172,296 , GRCh37.p13 chr17: 26,499,178-26,499,322 NLK
    nsv5711684mobile element insertion2nstd211human GRCh38 chr17: 28,104,929-28,104,929 , GRCh37.p13 chr17: 26,431,955-26,431,955 NLK
    nsv5710847mobile element insertion1nstd211human GRCh38 chr17: 28,048,179-28,048,179 , GRCh37.p13 chr17: 26,375,205-26,375,205 NLK, LOC102724517
    nsv5709192mobile element insertion1nstd211human GRCh38 chr17: 28,204,109-28,204,109 , GRCh37.p13 chr17: 26,531,135-26,531,135 LOC105371710, NLK
    nsv5708585mobile element insertion1nstd211human GRCh38 chr17: 28,168,038-28,168,038 , GRCh37.p13 chr17: 26,495,064-26,495,064 NLK
    nsv5662715insertion1nstd207human GRCh38 chr17: 28,172,116-28,172,116 , GRCh37.p13 chr17: 26,499,142-26,499,142 NLK
    nsv5657242insertion1nstd207human GRCh38 chr17: 28,104,911-28,104,911 , GRCh37.p13 chr17: 26,431,937-26,431,937 NLK
    nsv5649238insertion1nstd207human GRCh38 chr17: 28,172,264-28,172,264 , GRCh37.p13 chr17: 26,499,290-26,499,290 NLK
    nsv5601177copy number variation1nstd207human GRCh38 chr17: 28,172,116-28,172,169 , GRCh37.p13 chr17: 26,499,142-26,499,195 NLK
    nsv5529297copy number variation1nstd206human GRCh38 chr17: 28,141,688-28,142,247 , GRCh37.p13 chr17: 26,468,714-26,469,273 LOC105371711, NLK
    nsv5522372copy number variation1nstd206human GRCh38 chr17: 28,204,803-28,208,572 , GRCh37.p13 chr17: 26,531,829-26,535,598 LOC105371710, NLK
    nsv5521943copy number variation1nstd206human GRCh38 chr17: 28,170,339-28,170,497 , GRCh37.p13 chr17: 26,497,365-26,497,523 NLK
    nsv5519210copy number variation1nstd206human GRCh38 chr17: 28,186,902-28,186,990 , GRCh37.p13 chr17: 26,513,928-26,514,016 NLK
    nsv5518744copy number variation1nstd206human GRCh38 chr17: 28,112,796-28,112,871 , GRCh37.p13 chr17: 26,439,822-26,439,897 NLK
    nsv5515411copy number variation1nstd206human GRCh38 chr17: 28,159,745-28,159,958 , GRCh37.p13 chr17: 26,486,771-26,486,984 NLK
    nsv5429803mobile element insertion1nstd206human GRCh38 chr17: 28,204,109-28,204,160 , GRCh37.p13 chr17: 26,531,135-26,531,186 LOC105371710, NLK
    nsv5426181mobile element insertion1nstd206human GRCh38 chr17: 28,048,179-28,048,230 , GRCh37.p13 chr17: 26,375,205-26,375,256 NLK, LOC102724517
    nsv5374870translocation1nstd200human GRCh38 chr17: 28,204,836-28,204,836 , GRCh38 chr17: 28,208,671-28,208,671 , GRCh37.p13 chr17: 26,535,697-26,535,697 , GRCh37.p13 chr17: 26,531,862-26,531,862 LOC105371710, NLK
    nsv5358772translocation1nstd200human GRCh38 chr17: 28,170,497-28,170,497 , GRCh38 chr17: 28,170,339-28,170,339 , GRCh37.p13 chr17: 26,497,523-26,497,523 , GRCh37.p13 chr17: 26,497,365-26,497,365 NLK
    nsv5358771translocation1nstd200human GRCh38 chr17: 28,096,198-28,096,198 , GRCh38 chr17: 28,097,051-28,097,051 , GRCh37.p13 chr17: 26,424,077-26,424,077 , GRCh37.p13 chr17: 26,423,224-26,423,224 NLK
    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