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 236

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5696802mobile element insertion2nstd211human GRCh38 chr16: 69,957,770-69,957,770 , GRCh37.p13 chr16: 69,991,673-69,991,673 CLEC18A
    nsv5654084insertion1nstd207human GRCh38 chr16: 69,966,253-69,966,253 , GRCh37.p13 chr16: 70,000,156-70,000,156 CLEC18A
    nsv5647640insertion1nstd207human GRCh38 chr16: 69,962,928-69,962,928 , GRCh37.p13 chr16: 69,996,831-69,996,831 CLEC18A
    nsv5596259copy number variation1nstd207human GRCh38 chr16: 69,946,552-70,169,466 , GRCh37.p13 chr16: 69,980,455-70,203,369 PDPR, PDXDC2P-NPIPB14P, 6 more genes
    nsv5590561copy number variation1nstd207human GRCh38 chr16: 69,960,261-69,960,407 , GRCh37.p13 chr16: 69,994,164-69,994,310 CLEC18A
    nsv5552070insertion1nstd206human GRCh38 chr16: 69,954,373-69,954,423 , GRCh37.p13 chr16: 69,988,276-69,988,326 CLEC18A
    nsv5522937copy number variation1nstd206human GRCh38 chr16: 69,966,011-70,157,695 , GRCh37.p13 chr16: 69,999,914-70,191,598 PDPR, PDXDC2P-NPIPB14P, 6 more genes
    nsv5419243mobile element insertion1nstd206human GRCh38 chr16: 69,957,770-69,957,821 , GRCh37.p13 chr16: 69,991,673-69,991,724 CLEC18A
    nsv5299303copy number variation1nstd204human GRCh38.p13 chr16: 69,959,301-69,960,100 , GRCh37.p13 chr16: 69,993,204-69,994,003 CLEC18A
    nsv5296481copy number variation1nstd204human GRCh38.p13 chr16: 69,957,101-69,961,100 , GRCh37.p13 chr16: 69,991,004-69,995,003 CLEC18A
    nsv5296265copy number variation1nstd204human GRCh38.p13 chr16: 69,967,301-69,975,600 , GRCh37.p13 chr16: 70,001,204-70,009,503 PDXDC2P-NPIPB14P, NPIPB14P, 1 more genes
    nsv5293741copy number variation1nstd204human GRCh38.p13 chr16: 69,954,501-69,956,300 , GRCh37.p13 chr16: 69,988,404-69,990,203 CLEC18A
    nsv5291926copy number variation1nstd204human GRCh38.p13 chr16: 69,963,515-69,967,227 , GRCh37.p13 chr16: 69,997,418-70,001,130 CLEC18A
    nsv5291330copy number variation1nstd204human GRCh38.p13 chr16: 69,952,751-69,955,038 , GRCh37.p13 chr16: 69,986,654-69,988,941 CLEC18A
    nsv5290670copy number variation1nstd204human GRCh38.p13 chr16: 69,964,701-69,965,400 , GRCh37.p13 chr16: 69,998,604-69,999,303 CLEC18A
    nsv5289823copy number variation1nstd204human GRCh38.p13 chr16: 69,956,201-69,958,900 , GRCh37.p13 chr16: 69,990,104-69,992,803 CLEC18A
    nsv5286394copy number variation1nstd204human GRCh38.p13 chr16: 69,957,301-69,957,700 , GRCh37.p13 chr16: 69,991,204-69,991,603 CLEC18A
    nsv5284320copy number variation1nstd204human GRCh38.p13 chr16: 69,958,701-69,960,600 , GRCh37.p13 chr16: 69,992,604-69,994,503 CLEC18A
    nsv5283872copy number variation1nstd204human GRCh38.p13 chr16: 69,963,401-69,967,300 , GRCh37.p13 chr16: 69,997,304-70,001,203 CLEC18A
    nsv5283428copy number variation1nstd204human GRCh38.p13 chr16: 69,962,899-69,966,712 , GRCh37.p13 chr16: 69,996,802-70,000,615 CLEC18A
    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