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 363

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980315insertion1nstd209human GRCh38 chr12: 123,297,352-123,297,352 , GRCh37.p13 chr12: 123,781,899-123,781,899 SBNO1
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5972936insertion1nstd209human GRCh38 chr12: 123,299,699-123,299,699 , GRCh37.p13 chr12: 123,784,246-123,784,246 SBNO1
    nsv5940825copy number variation1nstd209human GRCh38 chr12: 123,302,185-123,302,495 , GRCh37.p13 chr12: 123,786,732-123,787,042 SBNO1
    nsv5939946copy number variation1nstd209human GRCh38 chr12: 123,346,438-123,348,604 , GRCh37.p13 chr12: 123,830,985-123,833,151 SBNO1
    nsv5935718copy number variation1nstd209human GRCh38 chr12: 123,311,625-123,312,009 , GRCh37.p13 chr12: 123,796,172-123,796,556 SBNO1
    nsv5935551copy number variation1nstd209human GRCh38 chr12: 123,310,280-123,310,580 , GRCh37.p13 chr12: 123,794,827-123,795,127 SBNO1
    nsv5933824copy number variation1nstd209human GRCh38 chr12: 123,349,530-123,349,592 , GRCh37.p13 chr12: 123,834,077-123,834,139 SBNO1
    nsv5933537copy number variation1nstd209human GRCh38 chr12: 123,353,393-123,354,225 , GRCh37.p13 chr12: 123,837,940-123,838,772 SBNO1
    nsv5855688copy number variation1nstd209human GRCh38 chr12: 123,346,396-123,348,536 , GRCh37.p13 chr12: 123,830,943-123,833,083 SBNO1
    nsv5848030copy number variation2nstd209human GRCh38 chr12: 123,346,296-123,347,936 , GRCh37.p13 chr12: 123,830,843-123,832,483 SBNO1
    nsv5705377mobile element insertion2nstd211human GRCh38 chr12: 123,336,292-123,336,292 , GRCh37.p13 chr12: 123,820,839-123,820,839 SBNO1
    nsv5696652mobile element insertion1nstd211human GRCh38 chr12: 123,303,702-123,303,702 , GRCh37.p13 chr12: 123,788,249-123,788,249 SBNO1
    nsv5592173copy number variation1nstd207human GRCh38 chr12: 123,349,530-123,349,592 , GRCh37.p13 chr12: 123,834,077-123,834,139 SBNO1
    nsv5590697copy number variation1nstd207human GRCh38 chr12: 123,297,329-123,297,400 , GRCh37.p13 chr12: 123,781,876-123,781,947 SBNO1
    nsv5542723insertion1nstd206human GRCh38 chr12: 123,341,892-123,341,892 , GRCh37.p13 chr12: 123,826,439-123,826,439 SBNO1
    nsv5508531copy number variation1nstd206human GRCh38 chr12: 123,349,532-123,349,593 , GRCh37.p13 chr12: 123,834,079-123,834,140 SBNO1
    nsv5508044copy number variation1nstd206human GRCh38 chr12: 123,361,084-123,362,666 , GRCh37.p13 chr12: 123,845,631-123,847,213 SBNO1
    nsv5506954copy number variation1nstd206human GRCh38 chr12: 123,289,211-123,289,473 , GRCh37.p13 chr12: 123,773,758-123,774,020 SBNO1
    nsv5506729copy number variation1nstd206human GRCh38 chr12: 123,310,338-123,310,639 , GRCh37.p13 chr12: 123,794,885-123,795,186 SBNO1
    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