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 191

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5945569copy number variation1nstd209human GRCh38 chr17: 78,975,104-78,975,185 , GRCh37.p13 chr17: 76,971,186-76,971,267 LGALS3BP
    nsv5934030copy number variation1nstd209human GRCh38 chr17: 78,903,527-78,994,644 , GRCh37.p13 chr17: 76,899,609-76,990,726 TIMP2, CEP295NL, 2 more genes
    nsv5869946copy number variation1nstd209human GRCh38 chr17: 78,957,717-78,980,930 , GRCh37.p13 chr17: 76,953,799-76,977,012 LGALS3BP
    nsv5519653copy number variation1nstd206human GRCh38 chr17: 78,975,790-78,975,886 , GRCh37.p13 chr17: 76,971,872-76,971,968 LGALS3BP
    nsv5016923copy number variation1nstd200human GRCh38 chr17: 78,979,302-78,983,391 , GRCh37.p13 chr17: 76,975,384-76,979,473 LGALS3BP
    nsv5016922copy number variation1nstd200human GRCh38 chr17: 78,978,889-78,984,799 , GRCh37.p13 chr17: 76,974,971-76,980,881 LGALS3BP
    nsv5016921copy number variation1nstd200human GRCh38 chr17: 78,975,790-78,975,886 , GRCh37.p13 chr17: 76,971,872-76,971,968 LGALS3BP
    nsv5016920copy number variation1nstd200human GRCh38 chr17: 78,970,530-78,972,343 , GRCh37.p13 chr17: 76,966,612-76,968,425 LGALS3BP
    nsv5014073copy number variation1nstd200human GRCh38 chr17: 78,919,633-79,477,545 , GRCh37.p13 chr17: 76,915,715-77,412,183 TIMP2, LGALS3BP, 5 more genes
    nsv4867421copy number variation1nstd200human GRCh37 chr17: 76,974,971-76,980,881 , GRCh38.p12 chr17: 78,978,889-78,984,799 LGALS3BP
    nsv4867420copy number variation1nstd200human GRCh37 chr17: 76,959,034-76,965,593 , GRCh38.p12 chr17: 78,962,952-78,969,511 LGALS3BP
    nsv4854415copy number variation1nstd200human GRCh37 chr17: 76,899,609-76,990,727 , GRCh38.p12 chr17: 78,903,527-78,994,645 CANT1, TIMP2, 2 more genes
    nsv4729773copy number variation1nstd102humanUncertain significance GRCh37 chr17: 76,852,029-77,297,898 , GRCh38.p12 chr17: 78,855,947-79,301,816 C1QTNF1, CANT1, 6 more genes
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4457695copy number variation2nstd102humanUncertain significance GRCh37 chr17: 76,857,398-77,308,782 , GRCh38.p12 chr17: 78,861,316-79,312,700 CEP295NL, C1QTNF1-AS1, 6 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4269967copy number variation1nstd166human GRCh37.p13 chr17: 76,971,872-76,971,968 , GRCh38.p12 chr17: 78,975,790-78,975,886 LGALS3BP
    nsv4264611copy number variation1nstd166human GRCh37.p13 chr17: 76,966,612-76,968,425 , GRCh38.p12 chr17: 78,970,530-78,972,343 LGALS3BP
    nsv4262682copy number variation1nstd166human GRCh37.p13 chr17: 76,967,671-76,971,895 , GRCh38.p12 chr17: 78,971,589-78,975,813 LGALS3BP
    nsv4262229copy number variation1nstd166human GRCh37.p13 chr17: 76,649,383-77,059,909 , GRCh38.p12 chr17: 78,653,301-79,063,827 , CEP295NL, 9 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