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 542

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121448copy number variation1nstd186human GRCh37 chr14: 81,469,147-81,469,427 , GRCh38.p12 chr14: 81,002,803-81,003,083 TSHR
    nsv6121419copy number variation1nstd186human GRCh37 chr14: 81,597,053-81,597,359 , GRCh38.p12 chr14: 81,130,709-81,131,015 LOC101928462, TSHR
    nsv6121261copy number variation1nstd186human GRCh37 chr14: 81,539,095-81,539,387 , GRCh38.p12 chr14: 81,072,751-81,073,043 LOC101928462, TSHR
    nsv5977563insertion1nstd209human GRCh38 chr14: 80,973,403-80,973,403 , GRCh37.p13 chr14: 81,439,747-81,439,747 TSHR
    nsv5973836insertion1nstd209human GRCh38 chr14: 81,069,164-81,069,164 , GRCh37.p13 chr14: 81,535,508-81,535,508 TSHR, LOC101928462
    nsv5971249insertion1nstd209human GRCh38 chr14: 81,094,679-81,094,679 , GRCh37.p13 chr14: 81,561,023-81,561,023 LOC101928462, TSHR
    nsv5968775insertion1nstd209human GRCh38 chr14: 81,037,423-81,037,423 , GRCh37.p13 chr14: 81,503,767-81,503,767 TSHR
    nsv5942827copy number variation1nstd209human GRCh38 chr14: 81,130,696-81,131,014 , GRCh37.p13 chr14: 81,597,040-81,597,358 LOC101928462, TSHR
    nsv5941913copy number variation1nstd209human GRCh38 chr14: 81,072,751-81,073,036 , GRCh37.p13 chr14: 81,539,095-81,539,380 TSHR, LOC101928462
    nsv5940915copy number variation1nstd209human GRCh38 chr14: 81,035,199-81,035,565 , GRCh37.p13 chr14: 81,501,543-81,501,909 TSHR
    nsv5939816copy number variation1nstd209human GRCh38 chr14: 81,131,941-81,132,021 , GRCh37.p13 chr14: 81,598,285-81,598,365 TSHR, LOC101928462
    nsv5932551copy number variation1nstd209human GRCh38 chr14: 81,029,767-81,029,912 , GRCh37.p13 chr14: 81,496,111-81,496,256 TSHR
    nsv5848433copy number variation1nstd209human GRCh38 chr14: 81,011,265-81,013,323 , GRCh37.p13 chr14: 81,477,609-81,479,667 , TSHR
    nsv5714981mobile element insertion2nstd211human GRCh38 chr14: 81,010,879-81,010,879 , GRCh37.p13 chr14: 81,477,223-81,477,223 TSHR
    nsv5708676mobile element insertion2nstd211human GRCh38 chr14: 81,033,524-81,033,524 , GRCh37.p13 chr14: 81,499,868-81,499,868 TSHR
    nsv5700851mobile element insertion2nstd211human GRCh38 chr14: 81,046,870-81,046,870 , GRCh37.p13 chr14: 81,513,214-81,513,214 TSHR
    nsv5699518mobile element insertion1nstd211human GRCh38 chr14: 81,126,508-81,126,508 , GRCh37.p13 chr14: 81,592,852-81,592,852 TSHR, LOC101928462
    nsv5660780insertion1nstd207human GRCh38 chr14: 81,010,864-81,010,864 , GRCh37.p13 chr14: 81,477,208-81,477,208 TSHR
    nsv5599586copy number variation1nstd207human GRCh38 chr14: 81,130,696-81,131,014 , GRCh37.p13 chr14: 81,597,040-81,597,358 LOC101928462, TSHR
    nsv5598283copy number variation1nstd207human GRCh38 chr14: 81,072,751-81,073,036 , GRCh37.p13 chr14: 81,539,095-81,539,380 TSHR, LOC101928462
    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