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 36

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3118369copy number variation1nstd149human GRCh37 chr8: 3,001,841-3,216,490 , GRCh38.p12 chr8: 3,144,319-3,358,968 CSMD1
    nsv3118376copy number variation1nstd149human GRCh37 chr1: 50,068,913-50,278,208 , GRCh38.p12 chr1: 49,603,241-49,812,536 AGBL4
    nsv3118385copy number variation1nstd149human GRCh37 chrX: 23,395,713-23,487,393 , GRCh38.p12 chrX: 23,377,596-23,469,276 PTCHD1
    nsv3118370copy number variation1nstd149human GRCh37 chr8: 3,128,806-3,196,713 , GRCh38.p12 chr8: 3,271,284-3,339,191 CSMD1
    nsv3118391copy number variation1nstd149human GRCh37 chr8: 4,232,020-4,287,861 , GRCh38.p12 chr8: 4,374,498-4,430,339 CSMD1
    nsv3118390copy number variation1nstd149human GRCh37 chr8: 3,141,292-3,184,031 , GRCh38.p12 chr8: 3,283,770-3,326,509 CSMD1
    nsv3118374copy number variation1nstd149human GRCh37 chr8: 2,999,931-3,022,135 , GRCh38.p12 chr8: 3,142,409-3,164,613 CSMD1
    nsv3118372copy number variation1nstd149human GRCh37 chr8: 99,524,409-99,546,574 , GRCh38.p12 chr8: 98,512,181-98,534,346 STK3
    nsv3118364copy number variation1nstd149human GRCh37 chr15: 37,328,986-37,332,249 , GRCh38.p12 chr15: 37,036,785-37,040,048 MEIS2
    nsv3118371copy number variation1nstd149human GRCh37 chr8: 3,832,830-4,391,617 , GRCh38.p12 chr8: 3,975,308-4,534,095 CSMD1, LOC105377789
    nsv3118368copy number variation1nstd149human GRCh37 chr8: 2,885,653-3,273,571 , GRCh38.p12 chr8: 3,028,131-3,416,049 CSMD1, LOC105377791
    nsv3118365copy number variation1nstd149human GRCh38.p12 chr1: 48,919,274-49,205,894 , GRCh37 chr1: 49,384,946-49,671,566 AGBL4, LOC105378706
    nsv3118360copy number variation4nstd149human GRCh38.p12 chr1: 49,785,058-49,939,698 , GRCh37 chr1: 50,250,730-50,405,370 AGBL4, ZNF859P
    nsv3118377copy number variation1nstd149human GRCh37 chr1: 50,251,479-50,398,437 , GRCh38.p12 chr1: 49,785,807-49,932,765 AGBL4, ZNF859P
    nsv3118358copy number variation2nstd149human GRCh38.p12 chr1: 49,755,153-49,900,689 , GRCh37 chr1: 50,220,825-50,366,361 AGBL4, ZNF859P
    nsv3118378copy number variation1nstd149human GRCh37 chrX: 23,269,452-23,364,920 , GRCh38.p12 chrX: 23,251,335-23,346,803 PTCHD1, PTCHD1-AS
    nsv3118392copy number variation1nstd149human GRCh37 chr8: 99,591,666-99,678,567 , GRCh38.p12 chr8: 98,579,438-98,666,339 STK3, LOC101928296
    nsv3118393copy number variation1nstd149human GRCh37 chr8: 99,638,463-99,719,599 , GRCh38.p12 chr8: 98,626,235-98,707,371 STK3, LOC101928296
    nsv3118389copy number variation1nstd149human GRCh37 chr1: 49,944,717-50,022,294 , GRCh38.p12 chr1: 49,479,045-49,556,622 AGBL4, LOC107984954
    nsv3118367copy number variation1nstd149human GRCh37 chr8: 2,646,965-3,228,228 , GRCh38.p12 chr8: 2,789,427-3,370,706 CSMD1, LOC105377785
    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