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 1372

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147451copy number variation1nstd232human GRCh37.p13 chrX: 1,755,808-1,755,886 , GRCh38.p12 chrX: 1,636,915-1,636,993 ASMT
    nsv7143543insertion1nstd232human GRCh37.p13 chrX: 1,729,451-1,729,451 , GRCh38.p12 chrX: 1,610,558-1,610,558 ASMT
    nsv7140646copy number variation1nstd232human GRCh37.p13 chrX: 1,755,840-1,755,915 , GRCh38.p12 chrX: 1,636,947-1,637,022 ASMT
    nsv7139062copy number variation1nstd232human GRCh37.p13 chrX: 1,715,634-1,715,784 , GRCh38.p12 chrX: 1,596,741-1,596,891 ASMT, AKAP17A
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098867copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-6,069,814 , GRCh38.p12 chrX: 284,188-6,151,773 RPL14P5, NLGN4X, 64 more genes
    nsv6636182copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,211,466-2,140,595 , GRCh38.p12 chrX: 1,111,313-2,222,554 SLC25A6, ASMTL, 17 more genes
    nsv6636164copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,734,398-2,140,501 , GRCh38.p12 chrX: 1,615,505-2,222,460 LOC105379413, DHRSX, 3 more genes
    nsv6636155copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,748,843-1,812,233 , GRCh38.p12 chrX: 1,629,950-1,693,340 ASMT
    nsv6636141copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,324,509-1,805,618 , GRCh38.p12 chrX: 1,205,616-1,686,725 IL3RA, LOC101928032, 11 more genes
    nsv6636130copy number variation1nstd102humanUncertain significance GRCh37 chrX: 852,805-1,717,093 , GRCh38.p12 chrX: 892,070-1,598,200 RPL14P5, ASMTL, 14 more genes
    nsv6636125copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,561,584-1,890,883 , GRCh38.p12 chrX: 1,442,691-1,771,990 ASMT, LINC02968, 4 more genes
    nsv6636090copy number variation1nstd102humanPathogenic GRCh37 chrX: 201,705-2,696,762 , GRCh38.p12 chrX: 285,038-2,778,721 ASMT, LINC00685, 33 more genes
    nsv6636053copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,752,332-2,387,869 , GRCh38.p12 chrX: 1,633,439-2,469,828 DHRSX, LOC105379413, 3 more genes
    nsv6636041copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,748,581-1,812,233 , GRCh38.p12 chrX: 1,629,688-1,693,340 ASMT
    nsv6636029copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,626,596-7,832,236 , GRCh38.p12 chrX: 1,507,703-7,864,195 ARSL, FAM239A, 53 more genes
    nsv6635563copy number variation1nstd227human GRCh37 chrX: 1,755,236-2,063,606 , GRCh38.p12 chrX: 1,636,343-1,944,713 ASMT, LINC02968, 2 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634094copy number variation4nstd224human GRCh37 chrY: 1-59,373,566 , GRCh38.p12 chrY: 10,001-57,217,415 ASMT, ASS1P6, 570 more genes
    nsv6315577complex substitution1nstd102humanPathogenic GRCh37 chrX: 590,376-56,315,041 , GRCh38.p12 chrX: 629,641-56,288,608 ACTG1P10, NR0B1, 778 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