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 119

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112768copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,984,696-46,405,042 , GRCh38.p12 chr5: 34,984,591-46,404,940 LIFR-AS1, FGF10-AS1, 137 more genes
    nsv5473575copy number variation1nstd206human GRCh38 chr5: 36,172,019-36,176,092 , GRCh37.p13 chr5: 36,172,121-36,176,194 SKP2
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv5083224mobile element insertion1nstd203human GRCh38 chr5: 36,183,953-36,183,969 , GRCh37.p13 chr5: 36,184,055-36,184,071 SKP2
    nsv4569390sequence alteration1nstd166human GRCh37.p13 chr5: 36,152,256-36,160,529 , GRCh38.p12 chr5: 36,152,154-36,160,427 SKP2, LMBRD2, 1 more genes
    nsv4547364insertion1nstd166human GRCh37.p13 chr5: 36,184,343-36,184,343 , GRCh38.p12 chr5: 36,184,241-36,184,241 SKP2
    nsv4456866copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,453,883-46,389,339 , GRCh38.p12 chr5: 34,453,778-46,389,237 LOC100506639, EEF1A1P19, 146 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4391849copy number variation1nstd171human GRCh37 chr5: 36,175,833-36,175,869 , GRCh38.p12 chr5: 36,175,731-36,175,767 SKP2
    nsv4123577copy number variation1nstd166human GRCh37.p13 chr5: 36,171,574-36,171,681 , GRCh38.p12 chr5: 36,171,472-36,171,579 SKP2
    nsv3923992copy number variation1nstd102humanPathogenic GRCh37 chr5: 50,093-46,115,086 , NCBI36 chr5: 103,093-46,150,843 , GRCh38 chr5: 49,978-46,114,984 LOC100130748, CDH10, 533 more genes
    nsv3920391copy number variation1nstd102humanPathogenic GRCh38 chr5: 35,201,559-61,903,141 , GRCh37 chr5: 35,201,661-61,198,968 , NCBI36 chr5: 35,237,418-61,234,725 KRT18P56, LINC01265, 290 more genes
    nsv3918728copy number variation1nstd102humanPathogenic GRCh38 chr5: 4,849,498-36,818,719 , NCBI36 chr5: 4,902,611-36,854,578 , GRCh37 chr5: 4,849,611-36,818,821 LINC02100, FTH1P10, 334 more genes
    nsv3917947copy number variation1nstd102humanPathogenic GRCh38 chr5: 35,700,480-45,260,029 , NCBI36 chr5: 35,736,339-45,295,888 , GRCh37 chr5: 35,700,582-45,260,131 LINC02104, LOC100132789, 134 more genes
    nsv3912686copy number variation1nstd102humanUncertain significance NCBI36 chr5: 36,129,944-37,043,924 , GRCh37.p13 chr5: 36,094,187-37,008,167 , GRCh38.p12 chr5: 36,094,085-37,008,065 SKP2, RANBP3L, 11 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
    nsv3911585copy number variation1nstd102humanPathogenic NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550 LINC02241, ATPSCKMT, 878 more genes
    nsv3911295copy number variation1nstd102humanPathogenic GRCh37 chr5: 54,954-45,649,963 , NCBI36 chr5: 107,954-45,685,720 , GRCh38 chr5: 54,839-45,649,861 PMCHL1, LINC02211, 532 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 MEGF10, LOC100128407, 2080 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