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 333

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148140copy number variation1nstd102humanPathogenic GRCh38 chrX: 23,730,430-32,849,918 , GRCh37.p13 chrX: 23,748,547-32,868,035 ARX, LOC107985632, 85 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7086546copy number variation1nstd229human GRCh38 chrX: 27,813,951-27,817,125 , GRCh37.p13 chrX: 27,832,068-27,835,242 MAGEB10
    nsv7086545copy number variation1nstd229human GRCh38 chrX: 27,811,101-27,814,300 , GRCh37.p13 chrX: 27,829,218-27,832,417 MAGEB10, LOC100420323
    nsv7086544copy number variation1nstd229human GRCh38 chrX: 27,800,507-27,806,479 , GRCh37.p13 chrX: 27,818,624-27,824,596 MAGEB10
    nsv7086538copy number variation1nstd229human GRCh38 chrX: 27,762,270-27,856,957 , GRCh37.p13 chrX: 27,780,387-27,875,074 LOC392436, MAGEB10, 2 more genes
    nsv7086101copy number variation1nstd229human GRCh38 chrX: 19,663,657-28,237,068 , GRCh37.p13 chrX: 19,681,775-28,255,185 MAGEB18, RPS6KA3, 89 more genes
    nsv6636147copy number variation1nstd102humanPathogenic GRCh37 chrX: 24,879,855-32,902,136 , GRCh38.p12 chrX: 24,861,738-32,884,019 RNA5SP500, MAGEB6, 64 more genes
    nsv6636122copy number variation1nstd102humanPathogenic GRCh37 chrX: 24,675,165-31,490,279 , GRCh38.p12 chrX: 24,657,048-31,472,162 SCARNA23, CKS1BP6, 65 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315577complex substitution1nstd102humanPathogenic GRCh37 chrX: 590,376-56,315,041 , GRCh38.p12 chrX: 629,641-56,288,608 ACTG1P10, NR0B1, 778 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6315330copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-57,841,304 , GRCh38.p12 chrX: 251,879-57,814,871 NPM1P9, UBE2E4P, 799 more genes
    nsv6313163copy number variation1nstd102humanUncertain significance GRCh37 chrX: 23,105,194-31,458,625 , GRCh38.p12 chrX: 23,087,077-31,440,508 H2BP7, MIR6134, 86 more genes
    nsv6137607copy number variation1nstd213human GRCh37 chrX: 4,160,000-52,130,001 , GRCh38.p12 chrX: 4,241,959-52,386,858 NR0B1, AMELX, 630 more genes
    nsv6137606copy number variation1nstd213human GRCh37 chrX: 2,750,000-52,110,001 , GRCh38.p12 chrX: 2,831,959-52,366,858 NR0B1, AMELX, 653 more genes
    nsv6137605copy number variation1nstd213human GRCh37 chrX: 2,680,000-52,110,001 , GRCh38.p12 chrX: 2,761,959-52,366,858 NR0B1, AMELX, 654 more genes
    nsv6137604copy number variation1nstd213human GRCh37 chrX: 2,670,000-49,230,001 , GRCh38.p12 chrX: 2,751,959-49,347,809 NR0B1, AMELX, 588 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