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 125

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5655886insertion1nstd207human GRCh38 chr19: 50,959,712-50,959,712 , GRCh37.p13 chr19: 51,462,968-51,462,968 KLK6, LOC105372442
    nsv5653884insertion1nstd207human GRCh38 chr19: 50,959,670-50,959,670 , GRCh37.p13 chr19: 51,462,926-51,462,926 KLK6, LOC105372442
    nsv5650942insertion1nstd207human GRCh38 chr19: 50,969,098-50,969,098 , GRCh37.p13 chr19: 51,472,354-51,472,354 LOC105372442, KLK6
    nsv5646789insertion1nstd207human GRCh38 chr19: 50,960,203-50,960,203 , GRCh37.p13 chr19: 51,463,459-51,463,459 KLK6, LOC105372442
    nsv5600825copy number variation1nstd207human GRCh38 chr19: 50,961,013-50,961,148 , GRCh37.p13 chr19: 51,464,269-51,464,404 LOC105372442, KLK6
    nsv5587682copy number variation1nstd207human GRCh38 chr19: 50,959,679-50,959,745 , GRCh37.p13 chr19: 51,462,935-51,463,001 KLK6, LOC105372442
    nsv5024833copy number variation1nstd200human GRCh38 chr19: 50,948,824-51,065,442 , GRCh37.p13 chr19: 51,452,080-51,568,699 , KLK11, 9 more genes
    nsv4865271copy number variation1nstd200human GRCh37 chr19: 51,452,080-51,568,699 , GRCh38.p12 chr19: 50,948,824-51,065,442 , KLK12, 9 more genes
    nsv4763793insertion1nstd199human GRCh37 chr19: 51,462,887-51,462,887 , GRCh38.p12 chr19: 50,959,631-50,959,631 KLK6, LOC105372442
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4676347copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,469,730-51,916,485 , GRCh38.p12 chr19: 49,966,473-51,413,231 VRK3, SYT3, 93 more genes
    nsv4634048copy number variation1nstd183human GRCh37 chr19: 51,409,215-51,497,644 , GRCh38.p12 chr19: 50,905,959-50,994,388 KLK7, KLK6, 5 more genes
    nsv4622278copy number variation2nstd183human GRCh37 chr19: 51,459,520-51,461,407 , GRCh38.p12 chr19: 50,956,264-50,958,151 KLK6, LOC105372442
    nsv4442069insertion1nstd175human GRCh37 chr19: 51,462,923-51,462,923 , GRCh38.p12 chr19: 50,959,667-50,959,667 KLK6, LOC105372442
    nsv4440303copy number variation1nstd175human GRCh37 chr19: 51,464,184-51,464,318 , GRCh38.p12 chr19: 50,960,928-50,961,062 KLK6, LOC105372442
    nsv4368703copy number variation1nstd173human GRCh37 chr19: 51,444,294-51,524,667 , GRCh38.p12 chr19: 50,941,038-51,021,411 KLK7, KLK6, 6 more genes
    nsv4321864inversion1nstd166human GRCh37.p13 chr19: 46,657,897-51,634,775 , GRCh38.p12 chr19: 46,154,640-51,131,518 , C5AR1, 288 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