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 585

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128620insertion1nstd186human GRCh37 chr1: 64,958,061-64,958,061 , GRCh38.p12 chr1: 64,492,378-64,492,378 CACHD1
    nsv5950970insertion1nstd209human GRCh38 chr1: 64,492,378-64,492,378 , GRCh37.p13 chr1: 64,958,061-64,958,061 CACHD1
    nsv5950864insertion1nstd209human GRCh38 chr1: 64,512,393-64,512,393 , GRCh37.p13 chr1: 64,978,076-64,978,076 CACHD1
    nsv5883833copy number variation1nstd209human GRCh38 chr1: 64,605,382-64,605,970 , GRCh37.p13 chr1: 65,071,065-65,071,653 CACHD1
    nsv5883442copy number variation1nstd209human GRCh38 chr1: 64,541,895-64,541,974 , GRCh37.p13 chr1: 65,007,578-65,007,657 CACHD1
    nsv5871757copy number variation1nstd209human GRCh38 chr1: 64,480,732-64,490,289 , GRCh37.p13 chr1: 64,946,415-64,955,972 CACHD1
    nsv5869970copy number variation1nstd209human GRCh38 chr1: 64,502,596-64,502,693 , GRCh37.p13 chr1: 64,968,279-64,968,376 CACHD1
    nsv5830118copy number variation1nstd209human GRCh38 chr1: 64,480,763-64,481,762 , GRCh37.p13 chr1: 64,946,446-64,947,445 CACHD1
    nsv5693894mobile element insertion1nstd211human GRCh38 chr1: 64,477,605-64,477,605 , GRCh37.p13 chr1: 64,943,288-64,943,288 CACHD1
    nsv5690806mobile element insertion1nstd211human GRCh38 chr1: 64,500,735-64,500,735 , GRCh37.p13 chr1: 64,966,418-64,966,418 CACHD1
    nsv5687348mobile element insertion2nstd211human GRCh38 chr1: 64,587,983-64,587,983 , GRCh37.p13 chr1: 65,053,666-65,053,666 CACHD1
    nsv5682282mobile element insertion1nstd211human GRCh38 chr1: 64,631,368-64,631,368 , GRCh37.p13 chr1: 65,097,051-65,097,051 CACHD1
    nsv5678092mobile element insertion1nstd211human GRCh38 chr1: 64,512,475-64,512,475 , GRCh37.p13 chr1: 64,978,158-64,978,158 CACHD1
    nsv5677449mobile element insertion2nstd211human GRCh38 chr1: 64,492,395-64,492,395 , GRCh37.p13 chr1: 64,958,078-64,958,078 CACHD1
    nsv5615270insertion1nstd207human GRCh38 chr1: 64,541,895-64,541,895 , GRCh37.p13 chr1: 65,007,578-65,007,578 CACHD1
    nsv5614023insertion1nstd207human GRCh38 chr1: 64,512,460-64,512,460 , GRCh37.p13 chr1: 64,978,143-64,978,143 CACHD1
    nsv5608249insertion1nstd207human GRCh38 chr1: 64,492,378-64,492,378 , GRCh37.p13 chr1: 64,958,061-64,958,061 CACHD1
    nsv5567152copy number variation1nstd207human GRCh38 chr1: 64,502,596-64,502,693 , GRCh37.p13 chr1: 64,968,279-64,968,376 CACHD1
    nsv5554293sequence alteration1nstd206human GRCh38 chr1: 64,605,969-64,605,971 , GRCh37.p13 chr1: 65,071,652-65,071,654 CACHD1
    nsv5551768insertion1nstd206human GRCh38 chr1: 64,588,806-64,588,850 , GRCh37.p13 chr1: 65,054,489-65,054,533 CACHD1
    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