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 153

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5929452copy number variation1nstd209human GRCh38 chr17: 6,412,133-13,962,466 , GRCh37.p13 chr17: 6,315,453-13,865,783 , PIK3R5-DT, 226 more genes
    nsv5518154copy number variation1nstd206human GRCh38 chr17: 7,200,922-7,654,532 , GRCh37.p13 chr17: 7,104,241-7,557,850 SNORA48, MPDU1-AS1, 47 more genes
    nsv5295633copy number variation1nstd204human GRCh38.p13 chr17: 7,571,601-7,692,600 , GRCh37.p13 chr17: 7,474,919-7,595,918 MPDU1-AS1, SENP3-EIF4A1, 15 more genes
    nsv5284241copy number variation1nstd204human GRCh38.p13 chr17: 7,363,101-7,796,500 , GRCh37.p13 chr17: 7,266,420-7,699,818 SAT2, TNFSF12, 35 more genes
    nsv5283638copy number variation1nstd204human GRCh38.p13 chr17: 6,923,801-7,855,300 , GRCh37.p13 chr17: 6,827,120-7,758,618 , TNFSF12, 74 more genes
    nsv5181992mobile element insertion1nstd203human GRCh38 chr17: 7,645,599-7,645,618 , GRCh37.p13 chr17: 7,548,917-7,548,936 ATP1B2
    nsv5015749copy number variation1nstd200human GRCh38 chr17: 7,643,800-7,649,777 , GRCh37.p13 chr17: 7,547,118-7,553,095 ATP1B2
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729929copy number variation1nstd102humanPathogenic GRCh37 chr17: 6,650,649-8,040,151 , GRCh38.p12 chr17: 6,747,330-8,136,833 CYB5D1, GPS2, 98 more genes
    nsv4683612copy number variation2nstd102humanUncertain significance GRCh37 chr17: 6,589,506-8,151,374 , GRCh38.p12 chr17: 6,686,187-8,248,056 ALOX12P2, DLG4, 124 more genes
    nsv4576135mobile element insertion1nstd166human GRCh37.p13 chr17: 7,548,917-7,548,917 , GRCh38.p12 chr17: 7,645,599-7,645,599 ATP1B2
    nsv4381895copy number variation1nstd173human GRCh37 chr17: 7,500,765-7,548,320 , GRCh38.p12 chr17: 7,597,447-7,645,002 TRUND-NNN6-1, SAT2, 3 more genes
    nsv3962544copy number variation1nstd168human GRCh38 chr17: 7,626,300-7,667,697 , GRCh37.p13 chr17: 7,529,618-7,571,015 SAT2, ATP1B2, 2 more genes
    nsv3923531copy number variation1nstd102humanPathogenic NCBI36 chr17: 7,322,238-8,279,567 , GRCh37 chr17: 7,381,514-8,338,842 , GRCh38 chr17: 7,478,195-8,435,524 SLC25A35, TRP-CGG1-3, 82 more genes
    nsv3918406copy number variation1nstd102humanUncertain significance NCBI36 chr17: 7,388,943-7,514,624 , GRCh38 chr17: 7,544,902-7,670,581 , GRCh37 chr17: 7,448,219-7,573,899 TRUND-NNN6-1, TNFSF12-TNFSF13, 17 more genes
    nsv3917059copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901 PSMB6, RNU6-1065P, 409 more genes
    nsv3915354copy number variation1nstd102humanPathogenic GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519 KIF1C-AS1, TMEM107, 433 more genes
    nsv3915260copy number variation1nstd102humandrug response GRCh38 chr17: 7,603,519-7,768,486 , GRCh37 chr17: 7,506,837-7,671,804 RPL29P2, TP53, 8 more genes
    nsv3913013copy number variation1nstd102humanPathogenic GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055 RPS4XP17, SNORA67, 289 more genes
    nsv3911050copy number variation1nstd102humanPathogenic GRCh38 chr17: 5,732,953-12,095,349 , GRCh37 chr17: 5,636,273-11,998,666 , NCBI36 chr17: 5,576,997-11,939,391 C17orf49, SPEM1, 209 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