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 98

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097134copy number variation1nstd102humanPathogenic GRCh37 chr5: 172,089,144-172,774,583 , GRCh38.p12 chr5: 172,662,141-173,347,580 RNA5SP200, MIR5003, 22 more genes
    nsv7096765copy number variation1nstd102humanUncertain significance GRCh37 chr5: 171,765,373-172,939,426 , GRCh38.p12 chr5: 172,338,369-173,512,423 MIR5003, LOC285591, 31 more genes
    nsv7057944inversion1nstd229human GRCh38 chr5: 172,134,356-176,589,266 , GRCh37.p13 chr5: 171,561,360-176,016,267 MIR10523, NIFKP2, 92 more genes
    nsv7038290inversion1nstd229human GRCh38 chr5: 172,489,078-179,485,008 , GRCh37.p13 chr5: 171,916,082-178,912,009 ZFP2, NHP2, 168 more genes
    nsv6797237copy number variation1nstd229human GRCh38 chr5: 173,140,401-173,386,000 , GRCh37.p13 chr5: 172,567,404-172,813,003 STC2, BNIP1, 8 more genes
    nsv6793348copy number variation1nstd229human GRCh38 chr5: 173,314,571-173,314,617 , GRCh37.p13 chr5: 172,741,574-172,741,620 STC2
    nsv6792770copy number variation1nstd229human GRCh38 chr5: 173,231,366-173,354,838 , GRCh37.p13 chr5: 172,658,369-172,781,841 MIR8056, MIR12118, 4 more genes
    nsv6792311copy number variation1nstd229human GRCh38 chr5: 173,307,247-173,314,650 , GRCh37.p13 chr5: 172,734,250-172,741,653 STC2
    nsv6784260copy number variation1nstd229human GRCh38 chr5: 173,328,359-173,328,809 , GRCh37.p13 chr5: 172,755,362-172,755,812 STC2
    nsv6782955copy number variation1nstd229human GRCh38 chr5: 172,218,701-173,333,400 , GRCh37.p13 chr5: 171,645,705-172,760,403 ATP6V0E1, MIR10523, 31 more genes
    nsv6781511copy number variation1nstd229human GRCh38 chr5: 170,662,244-174,111,903 , GRCh37.p13 chr5: 170,089,248-173,538,906 LOC101928093, LOC107986482, 79 more genes
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 287 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv5901718copy number variation1nstd209human GRCh38 chr5: 172,153,284-177,326,767 , GRCh37.p13 chr5: 171,580,288-176,753,768 , LOC107986487, 114 more genes
    nsv5410619mobile element insertion1nstd206human GRCh38 chr5: 173,312,710-173,312,761 , GRCh37.p13 chr5: 172,739,713-172,739,764 STC2
    nsv5362703translocation1nstd200human GRCh38 chr5: 173,313,852-173,313,852 , GRCh38 chr5: 173,314,134-173,314,134 , GRCh37.p13 chr5: 172,741,137-172,741,137 , GRCh37.p13 chr5: 172,740,855-172,740,855 STC2
    nsv5334033translocation1nstd200human GRCh37 chr5: 172,741,137-172,741,137 , GRCh37 chr5: 172,740,855-172,740,855 , GRCh38.p12 chr5: 173,313,852-173,313,852 , GRCh38.p12 chr5: 173,314,134-173,314,134 STC2
    nsv5225553copy number variation1nstd204human GRCh38.p13 chr5: 173,322,945-173,325,744 , GRCh37.p13 chr5: 172,749,948-172,752,747 STC2
    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