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 1121

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112816copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,887,031-16,308,753 , GRCh38.p12 chr16: 14,793,174-16,214,896 , GRCh38.p12 chr16|NT_187607.1: 326,909-1,872,893 NTAN1, MIR3179-1, 50 more genes
    nsv6112786copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,124,782-16,291,779 , GRCh38.p12 chr16: 15,030,925-16,197,922 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,855,918 RNU6-213P, LOC105371102, 25 more genes
    nsv5980403copy number variation3nstd102humanPathogenic, Uncertain significance GRCh37 chr16: 15,802,668-15,932,109 , GRCh38.p12 chr16|NT_187607.1: 1,366,822-1,496,241 , GRCh38.p12 chr16: 15,708,811-15,838,252 NDE1, MYH11
    nsv5977280insertion1nstd209human GRCh38 chr16: 15,821,935-15,821,935 , GRCh37.p13 chr16: 15,915,792-15,915,792 MYH11
    nsv5968785insertion1nstd209human GRCh38 chr16: 15,712,882-15,712,882 , GRCh37.p13 chr16: 15,806,739-15,806,739 MYH11, NDE1
    nsv5968650insertion1nstd209human GRCh38 chr16: 15,788,095-15,788,095 , GRCh37.p13 chr16: 15,881,952-15,881,952 MYH11
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5937733copy number variation1nstd209human GRCh38 chr16: 15,792,845-15,792,905 , GRCh37.p13 chr16: 15,886,702-15,886,762 MYH11
    nsv5936519copy number variation1nstd209human GRCh38 chr16: 15,801,624-15,801,919 , GRCh37.p13 chr16: 15,895,481-15,895,776 MYH11
    nsv5935214copy number variation1nstd209human GRCh38 chr16: 15,828,724-15,830,097 , GRCh37.p13 chr16: 15,922,581-15,923,954 MYH11
    nsv5934903copy number variation1nstd209human GRCh38 chr16: 15,829,873-15,830,007 , GRCh37.p13 chr16: 15,923,730-15,923,864 MYH11
    nsv5931071copy number variation1nstd209human GRCh38 chr16: 15,775,407-15,775,456 , GRCh37.p13 chr16: 15,869,264-15,869,313 MYH11
    nsv5929048copy number variation1nstd209human GRCh38 chr16: 15,742,850-15,743,202 , GRCh37.p13 chr16: 15,836,707-15,837,059 MYH11
    nsv5928138copy number variation1nstd209human GRCh38 chr16: 15,180,124-18,091,718 , GRCh37.p13 chr16: 15,273,981-18,185,575 , LOC102723692, 42 more genes
    nsv5871416copy number variation1nstd209human GRCh38 chr16: 15,829,138-15,830,137 , GRCh37.p13 chr16: 15,922,995-15,923,994 MYH11
    nsv5715258mobile element insertion2nstd211human GRCh38 chr16: 15,763,337-15,763,337 , GRCh37.p13 chr16: 15,857,194-15,857,194 MYH11
    nsv5698155mobile element insertion2nstd211human GRCh38 chr16: 15,788,095-15,788,095 , GRCh37.p13 chr16: 15,881,952-15,881,952 MYH11
    nsv5661627insertion1nstd207human GRCh38 chr16: 15,821,935-15,821,935 , GRCh37.p13 chr16: 15,915,792-15,915,792 MYH11
    nsv5587533copy number variation1nstd207human GRCh38 chr16: 15,775,407-15,775,456 , GRCh37.p13 chr16: 15,869,264-15,869,313 MYH11
    nsv5564302copy number variation1nstd102humanUncertain significance GRCh37 chr16: 15,808,760-15,932,115 , GRCh38.p12 chr16: 15,714,903-15,838,258 , GRCh38.p12 chr16|NT_187607.1: 1,372,914-1,496,247 NDE1, MYH11
    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