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 625

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096096copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr21: 43,160,998-47,754,702 , GRCh38.p12 chr21: 41,740,838-46,334,788 TSPEAR, LINC01424, 158 more genes
    nsv7072799inversion1nstd229human GRCh38 chr21: 41,886,117-43,786,596 , GRCh37.p13 chr21: 43,306,226-45,206,477 ZNF295-AS1, LINC01668, 57 more genes
    nsv7067411inversion1nstd229human GRCh38 chr21: 41,927,141-41,931,438 , GRCh37.p13 chr21: 43,347,250-43,351,547 C2CD2
    nsv7064889inversion1nstd229human GRCh38 chr21: 41,632,756-44,900,321 , GRCh37.p13 chr21: 43,052,916-46,320,236 RNU6-1150P, LOC105372824, 123 more genes
    nsv7037338copy number variation1nstd229human GRCh38 chr21: 41,903,663-41,910,920 , GRCh37.p13 chr21: 43,323,772-43,331,029 C2CD2
    nsv7035161copy number variation1nstd229human GRCh38 chr21: 41,540,401-41,986,300 , GRCh37.p13 chr21: 42,912,328-43,406,409 SNORA91, LINC00479, 13 more genes
    nsv7035056copy number variation1nstd229human GRCh38 chr21: 41,936,394-41,938,604 , GRCh37.p13 chr21: 43,356,503-43,358,713 C2CD2
    nsv7034819copy number variation1nstd229human GRCh38 chr21: 41,894,955-41,904,700 , GRCh37.p13 chr21: 43,315,064-43,324,809 C2CD2
    nsv7034178copy number variation1nstd229human GRCh38 chr21: 41,381,334-42,127,138 , GRCh37.p13 chr21: 42,753,261-43,547,248 SNORA91, UMODL1, 20 more genes
    nsv7031115copy number variation1nstd229human GRCh38 chr21: 41,931,001-41,933,400 , GRCh37.p13 chr21: 43,351,110-43,353,509 C2CD2
    nsv7030539copy number variation1nstd229human GRCh38 chr21: 41,943,525-41,943,708 , GRCh37.p13 chr21: 43,363,634-43,363,817 C2CD2
    nsv7030085copy number variation1nstd229human GRCh38 chr21: 41,930,013-41,933,383 , GRCh37.p13 chr21: 43,350,122-43,353,492 C2CD2
    nsv7027877copy number variation1nstd229human GRCh38 chr21: 41,944,452-41,949,096 , GRCh37.p13 chr21: 43,364,561-43,369,205 SNORA91, C2CD2
    nsv7026600copy number variation1nstd229human GRCh38 chr21: 41,879,894-41,934,176 , GRCh37.p13 chr21: 43,300,003-43,354,285 C2CD2, PRDM15
    nsv7025510copy number variation1nstd229human GRCh38 chr21: 41,905,313-41,905,352 , GRCh37.p13 chr21: 43,325,422-43,325,461 C2CD2
    nsv7021111copy number variation1nstd229human GRCh38 chr21: 41,930,001-41,932,300 , GRCh37.p13 chr21: 43,350,110-43,352,409 C2CD2
    nsv7020238copy number variation1nstd229human GRCh38 chr21: 41,903,825-41,907,781 , GRCh37.p13 chr21: 43,323,934-43,327,890 C2CD2
    nsv7019948copy number variation1nstd229human GRCh38 chr21: 40,558,832-43,971,067 , GRCh37.p13 chr21: 41,930,759-45,390,948 LOC105372821, PDXK, 86 more genes
    nsv7019375copy number variation1nstd229human GRCh38 chr21: 41,905,384-41,905,839 , GRCh37.p13 chr21: 43,325,493-43,325,948 C2CD2
    nsv7018109copy number variation1nstd229human GRCh38 chr21: 41,884,567-41,888,589 , GRCh37.p13 chr21: 43,304,676-43,308,698 C2CD2
    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