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 944

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145001insertion1nstd232human GRCh37.p13 chr18: 55,838,620-55,838,620 , GRCh38.p12 chr18: 58,171,388-58,171,388 NEDD4L
    nsv7137140copy number variation1nstd102humanPathogenic GRCh37 chr18: 55,020,078-56,892,966 , GRCh38.p12 chr18: 57,352,847-59,225,734 ATP8B1-AS1, ALPK2, 33 more genes
    nsv7095174copy number variation1nstd102humanLikely benign GRCh37 chr18: 56,018,203-56,063,501 , GRCh38.p12 chr18: 58,350,971-58,396,269 NEDD4L
    nsv7095173copy number variation1nstd102humanUncertain significance GRCh37 chr18: 55,833,000-56,063,501 , GRCh38.p12 chr18: 58,165,768-58,396,269 LOC105372143, NEDD4L
    nsv7094938copy number variation1nstd102humanUncertain significance GRCh37 chr18: 55,833,000-55,919,306 , GRCh38.p12 chr18: 58,165,768-58,252,074 LOC105372143, NEDD4L
    nsv7074298inversion1nstd229human GRCh38 chr18: 57,616,429-58,231,337 , GRCh37.p13 chr18: 55,283,661-55,898,569 LOC105372143, LOC105372140, 11 more genes
    nsv7073986inversion1nstd229human GRCh38 chr18: 58,292,435-58,317,112 , GRCh37.p13 chr18: 55,959,667-55,984,344 NEDD4L
    nsv7073526inversion1nstd229human GRCh38 chr18: 53,651,514-59,638,513 , GRCh37.p13 chr18: 51,177,884-57,305,745 MBD2, LOC105372145, 78 more genes
    nsv7066250inversion1nstd229human GRCh38 chr18: 54,862,924-58,506,448 , GRCh37.p13 chr18: 52,530,155-56,173,680 NARS1, FECH, 48 more genes
    nsv7064605inversion1nstd229human GRCh38 chr18: 58,076,742-58,076,862 , GRCh37.p13 chr18: 55,743,974-55,744,094 NEDD4L
    nsv7063248inversion1nstd229human GRCh38 chr18: 56,708,701-59,883,923 , GRCh37.p13 chr18: 54,375,932-57,551,155 MRPL37P1, RPS26P54, 49 more genes
    nsv7016616copy number variation1nstd229human GRCh38 chr18: 58,299,958-58,304,395 , GRCh37.p13 chr18: 55,967,190-55,971,627 NEDD4L
    nsv7016474copy number variation1nstd229human GRCh38 chr18: 58,398,240-58,398,284 , GRCh37.p13 chr18: 56,065,472-56,065,516 NEDD4L
    nsv7016276copy number variation1nstd229human GRCh38 chr18: 58,210,578-58,221,066 , GRCh37.p13 chr18: 55,877,810-55,888,298 NEDD4L
    nsv7016180copy number variation1nstd229human GRCh38 chr18: 58,089,280-58,095,641 , GRCh37.p13 chr18: 55,756,512-55,762,873 NEDD4L
    nsv7015611copy number variation1nstd229human GRCh38 chr18: 58,251,473-58,256,238 , GRCh37.p13 chr18: 55,918,705-55,923,470 NEDD4L
    nsv7015168copy number variation1nstd229human GRCh38 chr18: 58,096,449-58,100,827 , GRCh37.p13 chr18: 55,763,681-55,768,059 NEDD4L
    nsv7014688copy number variation1nstd229human GRCh38 chr18: 58,262,901-58,270,000 , GRCh37.p13 chr18: 55,930,133-55,937,232 NEDD4L
    nsv7013978copy number variation1nstd229human GRCh38 chr18: 58,263,129-58,279,856 , GRCh37.p13 chr18: 55,930,361-55,947,088 NEDD4L
    nsv7013844copy number variation1nstd229human GRCh38 chr18: 58,134,360-58,134,671 , GRCh37.p13 chr18: 55,801,592-55,801,903 NEDD4L
    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