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 114

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5835736copy number variation2nstd209human GRCh38 chr3: 195,094,231-195,095,530 , GRCh37.p13 chr3: 194,814,960-194,816,259 XXYLT1, XXYLT1-AS1
    nsv5835185copy number variation1nstd209human GRCh38 chr3: 195,094,731-195,096,660 , GRCh37.p13 chr3: 194,815,460-194,817,389 XXYLT1, XXYLT1-AS1
    nsv5835184copy number variation1nstd209human GRCh38 chr3: 195,092,944-195,128,678 , GRCh37.p13 chr3: 194,813,673-194,849,407 XXYLT1-AS1, XXYLT1
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5233507copy number variation1nstd204human GRCh38.p13 chr3: 195,092,701-195,093,000 , GRCh37.p13 chr3: 194,813,430-194,813,729 XXYLT1, XXYLT1-AS1
    nsv4769367copy number variation1nstd102humanUncertain significance GRCh37 chr3: 194,498,718-196,196,789 , GRCh38.p12 chr3: 194,777,989-196,469,918 DYNLT2B, RNU6-25P, 56 more genes
    nsv4685587copy number variation1nstd102humannot provided GRCh37 chr3: 194,161,542-194,998,084 , GRCh38.p12 chr3: 194,440,813-195,277,355 RPL23AP93, LSG1, 22 more genes
    nsv4520275copy number variation1nstd166human GRCh37.p13 chr3: 194,813,999-194,938,000 , GRCh38.p12 chr3: 195,093,270-195,217,271 XXYLT1, MIR3137, 5 more genes
    nsv4436392copy number variation1nstd102humanPathogenic GRCh37 chr3: 188,386,566-197,838,262 , GRCh38.p12 chr3: 188,668,778-198,111,391 PPP1R2, GCNT1P3, 194 more genes
    nsv4408030copy number variation1nstd174human GRCh37 chr3: 194,708,030-195,237,488 , GRCh38.p12 chr3: 194,987,301-195,510,679 XXYLT1, LOC105374296, 9 more genes
    nsv4388059copy number variation1nstd173human GRCh37 chr3: 194,573,848-197,176,516 , GRCh38.p12 chr3: 194,853,119-197,449,645 , PIGX, 87 more genes
    nsv3924766copy number variation1nstd102humanPathogenic GRCh38 chr3: 194,424,496-198,168,758 , NCBI36 chr3: 195,626,514-199,380,026 , GRCh37 chr3: 194,145,225-197,895,629 XXYLT1, PIGZ, 119 more genes
    nsv3924195copy number variation1nstd102humanPathogenic GRCh38 chr3: 193,704,605-198,125,115 , NCBI36 chr3: 194,905,088-199,336,383 , GRCh37 chr3: 193,422,394-197,851,986 LOC105374298, LINC01983, 139 more genes
    nsv3922385copy number variation1nstd102humanPathogenic NCBI36 chr3: 177,369,007-199,329,651 , GRCh37 chr3: 175,886,313-197,845,254 , GRCh38 chr3: 176,168,525-198,118,383 LINC02053, RTP4, 414 more genes
    nsv3921532copy number variation1nstd102humanPathogenic GRCh38 chr3: 190,667,663-198,110,178 , NCBI36 chr3: 191,868,146-199,321,446 , GRCh37 chr3: 190,385,452-197,837,049 LOC105374282, PIGX, 173 more genes
    nsv3920662copy number variation1nstd102humanPathogenic NCBI36 chr3: 178,729,187-199,321,446 , GRCh37.p13 chr3: 177,246,493-197,837,049 , GRCh38.p12 chr3: 177,528,705-198,110,178 RN7SKP265, RPL24P6, 401 more genes
    nsv3920607copy number variation1nstd102humanPathogenic NCBI36 chr3: 187,082,628-197,946,692 , GRCh37.p13 chr3: 185,599,934-196,462,295 , GRCh38.p12 chr3: 185,882,146-196,735,424 FGF12, RFC4, 212 more genes
    nsv3920444copy number variation1nstd102humanPathogenic NCBI36 chr3: 195,540,958-198,905,009 , GRCh38 chr3: 194,338,534-197,693,741 , GRCh37 chr3: 194,059,263-197,420,612 RN7SL36P, RPS29P3, 107 more genes
    nsv3920067copy number variation1nstd102humanPathogenic GRCh38 chr3: 189,265,371-198,110,178 , NCBI36 chr3: 190,465,854-199,321,446 , GRCh37 chr3: 188,983,160-197,837,049 OSTN-AS1, ACAP2, 188 more genes
    nsv3918982copy number variation1nstd102humanPathogenic GRCh37 chr3: 167,885,356-197,837,049 , NCBI36 chr3: 169,368,050-199,321,446 , GRCh38 chr3: 168,167,568-198,110,178 EIF4G1, LOC105374248, 515 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