U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Nucleotide

Items: 1 to 20 of 393

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5389014copy number variation1nstd186human GRCh37 chr7: 154,266,245-154,267,354 , GRCh38.p12 chr7|NW_012132919.1: 146,809-147,918 , GRCh38.p12 chr7: 154,569,160-154,570,269 DPP6
    nsv5345554translocation1nstd200human GRCh37 chr7: 154,238,749-154,238,749 , GRCh37 chr7: 154,241,019-154,241,019 , GRCh38.p12 chr7|NW_012132919.1: 119,313-119,313 , GRCh38.p12 chr7|NW_012132919.1: 121,583-121,583 , GRCh38.p12 chr7: 154,543,934-154,543,934 , GRCh38.p12 chr7: 154,541,664-154,541,664 , DPP6
    nsv5329709translocation1nstd200human GRCh37 chr7: 154,153,823-154,153,823 , GRCh37 chr7: 154,155,070-154,155,070 , GRCh38.p12 chr7: 154,457,985-154,457,985 , GRCh38.p12 chr7|NW_012132919.1: 34,387-34,387 , GRCh38.p12 chr7: 154,456,738-154,456,738 , GRCh38.p12 chr7|NW_012132919.1: 35,634-35,634 DPP6
    nsv4825458copy number variation1nstd200human GRCh37 chr7: 154,135,602-154,234,884 , GRCh38.p12 chr7: 154,438,517-154,537,799 , GRCh38.p12 chr7|NW_012132919.1: 16,166-115,448 DPP6
    nsv4812559copy number variation1nstd200human GRCh37 chr7: 154,266,192-154,267,590 , GRCh38.p12 chr7: 154,569,107-154,570,505 , GRCh38.p12 chr7|NW_012132919.1: 146,756-148,154 DPP6
    nsv4812558copy number variation1nstd200human GRCh37 chr7: 154,252,341-154,253,834 , GRCh38.p12 chr7: 154,555,256-154,556,749 , GRCh38.p12 chr7|NW_012132919.1: 132,905-134,398 , DPP6
    nsv4812557copy number variation1nstd200human GRCh37 chr7: 154,193,229-154,201,302 , GRCh38.p12 chr7|NW_012132919.1: 73,793-81,866 , GRCh38.p12 chr7: 154,496,144-154,504,217 DPP6
    nsv4812556copy number variation1nstd200human GRCh37 chr7: 154,178,350-154,412,424 , GRCh38.p12 chr7|NW_012132919.1: 58,914-179,932 , GRCh38.p12 chr7: 154,481,265-154,620,714 , LOC105375581, 1 more genes
    nsv4812555copy number variation1nstd200human GRCh37 chr7: 154,175,795-154,181,479 , GRCh38.p12 chr7|NW_012132919.1: 56,359-62,043 , GRCh38.p12 chr7: 154,478,710-154,484,394 DPP6
    nsv4751317insertion1nstd199human GRCh37 chr7: 154,382,273-154,382,273 , GRCh38.p12 chr7|NW_012132919.1: 167,558-167,558 , GRCh38.p12 chr7: 154,590,563-154,590,563 DPP6
    nsv4746089copy number variation1nstd199human GRCh37 chr7: 154,153,816-154,155,076 , GRCh38.p12 chr7|NW_012132919.1: 34,380-35,640 , GRCh38.p12 chr7: 154,456,731-154,457,991 DPP6
    nsv4743876copy number variation1nstd199human GRCh37 chr7: 154,128,527-154,128,587 , GRCh38.p12 chr7: 154,431,442-154,431,502 , GRCh38.p12 chr7|NW_012132919.1: 9,091-9,151 DPP6
    nsv4731217copy number variation1nstd199human GRCh37 chr7: 154,140,691-154,140,779 , GRCh38.p12 chr7|NW_012132919.1: 21,255-21,343 , GRCh38.p12 chr7: 154,443,606-154,443,694 DPP6
    nsv4711596copy number variation1nstd195human GRCh37 chr7: 154,391,901-154,391,902 , GRCh38.p12 chr7|NW_012132919.1: 177,186-177,187 , GRCh38.p12 chr7: 154,600,191-154,600,192 DPP6
    nsv4704614copy number variation2nstd195human GRCh37 chr7: 154,153,811-154,153,812 , GRCh38.p12 chr7: 154,456,726-154,456,727 , GRCh38.p12 chr7|NW_012132919.1: 34,375-34,376 DPP6
    nsv4659519copy number variation1nstd186human GRCh37 chr7: 154,266,246-154,267,496 , GRCh38.p12 chr7: 154,569,161-154,570,411 , GRCh38.p12 chr7|NW_012132919.1: 146,810-148,060 DPP6
    nsv4658467copy number variation1nstd186human GRCh37 chr7: 154,266,146-154,267,642 , GRCh38.p12 chr7|NW_012132919.1: 146,710-148,206 , GRCh38.p12 chr7: 154,569,061-154,570,557 DPP6
    nsv4634755copy number variation3nstd186human GRCh37 chr7: 154,153,823-154,155,070 , GRCh38.p12 chr7|NW_012132919.1: 34,387-35,634 , GRCh38.p12 chr7: 154,456,738-154,457,985 DPP6
    nsv4607879copy number variation2nstd183human GRCh37 chr7: 154,266,246-154,267,496 , GRCh38.p12 chr7: 154,569,161-154,570,411 , GRCh38.p12 chr7|NW_012132919.1: 146,810-148,060 DPP6
    nsv4602933copy number variation1nstd183human GRCh37 chr7: 154,266,146-154,267,642 , GRCh38.p12 chr7|NW_012132919.1: 146,710-148,206 , GRCh38.p12 chr7: 154,569,061-154,570,557 DPP6
    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