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 481

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7090574copy number variation1nstd229human GRCh38 chrX: 102,944,319-102,950,040 , GRCh37.p13 chrX: 102,199,247-102,204,968 LINC00630
    nsv7090573copy number variation1nstd229human GRCh38 chrX: 102,942,605-102,970,111 , GRCh37.p13 chrX: 102,197,533-102,225,039 LINC00630
    nsv7090572copy number variation1nstd229human GRCh38 chrX: 102,921,226-102,935,636 , GRCh37.p13 chrX: 102,176,154-102,190,564 RAB40AL, LINC00630
    nsv7090571copy number variation1nstd229human GRCh38 chrX: 102,907,839-102,917,687 , GRCh37.p13 chrX: 102,162,767-102,172,615 LINC00630, ARMCX5-GPRASP2
    nsv7090570copy number variation1nstd229human GRCh38 chrX: 102,906,561-102,921,056 , GRCh37.p13 chrX: 102,161,489-102,175,984 ARMCX5-GPRASP2, LINC00630
    nsv7090569copy number variation1nstd229human GRCh38 chrX: 102,880,101-102,882,900 , GRCh37.p13 chrX: 102,135,029-102,137,828 ARMCX5-GPRASP2, LINC00630
    nsv7090568copy number variation1nstd229human GRCh38 chrX: 102,864,348-102,865,385 , GRCh37.p13 chrX: 102,119,276-102,120,313 ARMCX5-GPRASP2, LINC00630
    nsv7090567copy number variation1nstd229human GRCh38 chrX: 102,843,501-103,234,900 , GRCh37.p13 chrX: 102,098,429-102,489,828 LINC00630, NUDT19P2, 7 more genes
    nsv7090566copy number variation1nstd229human GRCh38 chrX: 102,834,904-102,835,046 , GRCh37.p13 chrX: 102,089,832-102,089,974 ARMCX5-GPRASP2, LINC00630
    nsv7090565copy number variation1nstd229human GRCh38 chrX: 102,822,411-102,849,324 , GRCh37.p13 chrX: 102,077,339-102,104,252 ARMCX5-GPRASP2, LINC00630
    nsv7090564copy number variation1nstd229human GRCh38 chrX: 102,799,501-102,826,600 , GRCh37.p13 chrX: 102,054,429-102,081,528 MTCYBP32, LINC00630, 6 more genes
    nsv7090563copy number variation1nstd229human GRCh38 chrX: 102,791,601-102,795,200 , GRCh37.p13 chrX: 102,046,529-102,050,128 LINC00630, ARMCX5-GPRASP2, 1 more genes
    nsv7090562copy number variation1nstd229human GRCh38 chrX: 102,791,501-102,802,800 , GRCh37.p13 chrX: 102,046,429-102,057,728 MTCO1P19, MTCO3P19, 6 more genes
    nsv7090561copy number variation1nstd229human GRCh38 chrX: 102,788,301-102,801,400 , GRCh37.p13 chrX: 102,043,229-102,056,328 MTCO2P19, MTND2P2, 6 more genes
    nsv7090560copy number variation1nstd229human GRCh38 chrX: 102,788,201-102,801,300 , GRCh37.p13 chrX: 102,043,129-102,056,228 MTCO3P19, MTCO1P19, 6 more genes
    nsv7090551copy number variation1nstd229human GRCh38 chrX: 102,567,983-102,865,175 , GRCh37.p13 chrX: 101,822,911-102,120,103 GPRASP1, H3P45, 18 more genes
    nsv7090477copy number variation1nstd229human GRCh38 chrX: 101,314,695-102,956,469 , GRCh37.p13 chrX: 100,569,683-102,211,397 LOC105373299, RPL21P132, 59 more genes
    nsv7057375inversion1nstd229human GRCh38 chrX: 102,801,345-102,880,122 , GRCh37.p13 chrX: 102,056,273-102,135,050 MTND5P26, MTCYBP32, 4 more genes
    nsv7057180inversion1nstd229human GRCh38 chrX: 102,943,038-102,943,080 , GRCh37.p13 chrX: 102,197,966-102,198,008 LINC00630
    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