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 289

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5321894copy number variation1nstd204human GRCh38.p13 chr18: 36,169,111-36,169,527 , GRCh37.p13 chr18: 33,749,074-33,749,490 ELP2
    nsv5295502copy number variation1nstd204human GRCh38.p13 chr18: 36,132,995-36,143,034 , GRCh37.p13 chr18: 33,712,958-33,722,997 ELP2
    nsv5293801copy number variation1nstd204human GRCh37.p13 chr18: 33,436,764-33,759,363 , GRCh38.p13 chr18: 35,856,801-36,179,400 SLC39A6, RPRD1A, 6 more genes
    nsv5011355copy number variation1nstd200human GRCh38 chr18: 36,160,939-36,163,925 , GRCh37.p13 chr18: 33,740,902-33,743,888 ELP2
    nsv4729854copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,971,647-33,737,300 , GRCh38.p12 chr18: 26,391,683-36,157,337 CLUHP6, KLHL14, 100 more genes
    nsv4676233copy number variation1nstd102humanPathogenic GRCh37 chr18: 22,868,759-34,335,753 , GRCh38.p12 chr18: 25,288,795-36,755,790 DHFRP1, CLUHP6, 116 more genes
    nsv4676192copy number variation1nstd102humanUncertain significance GRCh37 chr18: 33,384,923-34,561,159 , GRCh38.p12 chr18: 35,804,959-36,981,196 LOC105372071, ELP2, 15 more genes
    nsv4676155copy number variation1nstd102humanPathogenic GRCh37 chr18: 20,689,919-49,455,212 , GRCh38.p12 chr18: 23,109,955-51,928,842 KLHL14, RPL23AP77, 318 more genes
    nsv4350805copy number variation1nstd102humanPathogenic GRCh37 chr18: 33,554,981-36,939,357 , GRCh38.p12 chr18: 35,975,018-39,359,393 LOC101927879, LOC105372076, 28 more genes
    nsv4336672sequence alteration1nstd166human GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628 , CDH2, 557 more genes
    nsv4268357copy number variation1nstd166human GRCh37.p13 chr18: 33,732,198-33,732,342 , GRCh38.p12 chr18: 36,152,235-36,152,379 ELP2
    nsv4262920copy number variation1nstd166human GRCh37.p13 chr18: 33,758,565-33,758,660 , GRCh38.p12 chr18: 36,178,602-36,178,697 ELP2, COSMOC
    nsv4261040copy number variation1nstd166human GRCh37.p13 chr18: 33,738,488-33,738,608 , GRCh38.p12 chr18: 36,158,525-36,158,645 ELP2
    nsv4260414copy number variation1nstd166human GRCh37.p13 chr18: 33,710,917-33,711,029 , GRCh38.p12 chr18: 36,130,954-36,131,066 ELP2
    nsv4257575copy number variation1nstd166human GRCh37.p13 chr18: 33,735,868-33,736,949 , GRCh38.p12 chr18: 36,155,905-36,156,986 ELP2
    nsv4256255copy number variation1nstd166human GRCh37.p13 chr18: 33,717,127-33,718,164 , GRCh38.p12 chr18: 36,137,164-36,138,201 ELP2
    nsv3960846copy number variation1nstd168human GRCh38 chr18: 36,152,775-36,168,600 , GRCh37.p13 chr18: 33,732,738-33,748,563 ELP2
    nsv3924706copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097 LOC100420948, NPM1P2, 941 more genes
    nsv3924638copy number variation1nstd102humanPathogenic GRCh38 chr18: 20,962,119-74,691,446 , NCBI36 chr18: 16,796,078-70,532,390 , GRCh37 chr18: 18,542,080-72,403,402 HMGN1P30, LOC107985134, 596 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