U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 94

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2756991copy number variation3estd1human NCBI35 chr3: 60,775,739-60,919,051 , GRCh37.p13 chr3|NW_003871058.1: 272,500-385,741 , GRCh37.p13 chr3: 60,830,770-60,944,011 , GRCh38.p12 chr3: 60,814,994-60,958,339 FHIT
    esv2756879copy number variation5estd1human NCBI35 chr1: 192,622,899-192,752,192 , GRCh37.p13 chr1: 195,891,242-196,020,535 , GRCh38.p12 chr1: 195,922,112-196,051,405 LINC01724
    esv2757562copy number variation48estd1human NCBI35 chr14: 40,646,835-40,769,154 , GRCh37.p13 chr14: 41,577,085-41,699,404 , GRCh38.p12 chr14: 41,107,880-41,230,201 LINC02315
    esv2757054copy number variation56estd1human NCBI35 chr4: 34,579,485-34,680,339 , GRCh37.p13 chr4|NW_003315915.1: 247,626-348,480 , GRCh37.p13 chr4: 34,756,919-34,857,773 , GRCh38.p12 chr4: 34,755,297-34,856,151 , GRCh38.p12 chr4|NW_003315915.1: 247,626-348,480 LOC105378262
    esv2757678copy number variation5estd1human NCBI35 chr18: 54,081,842-54,095,115 , GRCh37.p13 chr18: 55,930,862-55,944,135 , GRCh38.p12 chr18: 58,263,630-58,276,903 NEDD4L
    esv2756956copy number variation2estd1human GRCh38.p12 chr2: 186,551,872-186,628,015 , NCBI35 chr2: 187,242,105-187,318,248 , GRCh37.p13 chr2: 187,416,599-187,492,742 ITGAV
    esv2757787copy number variation190estd1human GRCh38.p12 chr2: 22,591,267-22,897,147 , NCBI35 chr2: 22,725,791-23,031,671 , GRCh37.p13 chr2: 22,814,139-23,120,019 RN7SKP27
    esv2757873copy number variation3estd1human GRCh37.p13 chr3: 61,019,003-61,185,558 , GRCh38.p12 chr3: 61,033,331-61,199,884 , NCBI35 chr3: 60,994,043-61,160,598 FHIT
    esv2758064copy number variation112estd1human GRCh38.p12 chr6: 78,086,163-78,483,751 , NCBI35 chr6: 78,852,599-79,250,187 , GRCh37.p13 chr6: 78,795,880-79,193,468 LOC105377865
    esv2758280copy number variation39estd1human NCBI35 chr11: 88,083,993-88,339,832 , GRCh37.p13 chr11: 88,444,345-88,700,184 , GRCh38.p12 chr11: 88,711,177-88,967,016 GRM5
    esv2757951copy number variation95estd1human GRCh38.p12 chr4: 116,601,155-116,699,723 , GRCh37.p13 chr4: 117,522,311-117,620,879 , NCBI35 chr4: 117,879,914-117,978,482 LOC105377385
    esv2757125copy number variation2estd1human NCBI35 chr5: 100,570,013-100,684,490 , GRCh37.p13 chr5: 100,542,114-100,656,591 , GRCh38.p12 chr5: 101,206,410-101,320,887 GTF3AP4, LOC107986438
    esv2757872copy number variation3estd1human GRCh37.p13 chr3: 60,781,943-61,019,003 , GRCh38.p12 chr3: 60,796,210-61,033,331 , NCBI35 chr3: 60,756,983-60,994,043 , GRCh37.p13 chr3|NW_003871058.1: 272,500-393,769 FHIT, LOC105377111
    esv2757967copy number variation264estd1human GRCh38.p12 chr4: 167,813,440-168,130,542 , GRCh37.p13 chr4: 168,734,591-169,051,693 , NCBI35 chr4: 169,109,321-169,426,423 ANXA10, LOC105377523
    esv2758007copy number variation2estd1human NCBI35 chr5: 100,535,625-100,788,621 , GRCh37.p13 chr5: 100,507,726-100,760,722 , GRCh38.p12 chr5: 101,172,022-101,425,018 GTF3AP4, LOC107986438
    esv2757269copy number variation92estd1human GRCh38.p12 chr8: 39,316,760-39,600,880 , NCBI35 chr8: 39,293,436-39,577,556 , GRCh37.p13 chr8: 39,174,279-39,458,399 ADAM3A, ADAM18, 2 more genes
    esv2757426copy number variation52estd1human NCBI35 chr11: 18,886,391-18,939,210 , GRCh37.p13 chr11: 18,929,815-18,982,634 , GRCh38.p12 chr11: 18,908,268-18,961,087 MRGPRX1, MRGPRX5P, 1 more genes
    esv2757436copy number variation2estd1human NCBI35 chr11: 34,869,891-34,920,304 , GRCh37.p13 chr11: 34,913,315-34,963,728 , GRCh38.p12 chr11: 34,891,768-34,942,181 PDHX, APIP, 1 more genes
    esv2757151copy number variation182estd1human GRCh38.p12 chr6: 217,334-411,954 , NCBI35 chr6: 162,334-356,954 , GRCh37.p13 chr6: 217,334-411,954 IRF4, DUSP22, 3 more genes
    esv2758167copy number variation17estd1human NCBI35 chr8: 100,473,327-100,907,800 , GRCh37.p13 chr8: 100,404,151-100,838,624 , GRCh38.p12 chr8: 99,391,923-99,826,396 VPS13B, MIR599, 3 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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