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 669

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114637mobile element insertion1nstd186human GRCh37 chr11: 36,173,610-36,173,661 , GRCh38.p12 chr11: 36,152,060-36,152,111 LDLRAD3
    nsv6114129mobile element insertion1nstd186human GRCh37 chr11: 36,061,047-36,061,055 , GRCh38.p12 chr11: 36,039,497-36,039,505 LDLRAD3
    nsv5979259insertion1nstd209human GRCh38 chr11: 35,986,025-35,986,025 , GRCh37.p13 chr11: 36,007,575-36,007,575 LDLRAD3
    nsv5973997insertion1nstd209human GRCh38 chr11: 36,055,104-36,055,104 , GRCh37.p13 chr11: 36,076,654-36,076,654 LDLRAD3
    nsv5972630insertion1nstd209human GRCh38 chr11: 36,128,141-36,128,141 , GRCh37.p13 chr11: 36,149,691-36,149,691 LDLRAD3
    nsv5970803insertion1nstd209human GRCh38 chr11: 36,152,043-36,152,043 , GRCh37.p13 chr11: 36,173,593-36,173,593 LDLRAD3
    nsv5924291copy number variation1nstd209human GRCh38 chr11: 36,081,390-36,081,459 , GRCh37.p13 chr11: 36,102,940-36,103,009 LDLRAD3
    nsv5918496copy number variation1nstd209human GRCh38 chr11: 36,170,231-36,170,305 , GRCh37.p13 chr11: 36,191,781-36,191,855 LDLRAD3
    nsv5915226copy number variation1nstd209human GRCh38 chr11: 36,102,131-36,103,481 , GRCh37.p13 chr11: 36,123,681-36,125,031 LDLRAD3
    nsv5909747copy number variation1nstd209human GRCh38 chr11: 35,941,890-35,942,023 , GRCh37.p13 chr11: 35,963,440-35,963,573 LDLRAD3
    nsv5908370copy number variation1nstd209human GRCh38 chr11: 36,158,493-36,160,750 , GRCh37.p13 chr11: 36,180,043-36,182,300 LDLRAD3
    nsv5865540copy number variation1nstd209human GRCh38 chr11: 36,158,643-36,160,842 , GRCh37.p13 chr11: 36,180,193-36,182,392 LDLRAD3
    nsv5854758copy number variation1nstd209human GRCh38 chr11: 36,102,196-36,103,495 , GRCh37.p13 chr11: 36,123,746-36,125,045 LDLRAD3
    nsv5728883mobile element insertion1nstd211human GRCh38 chr11: 36,016,664-36,016,664 , GRCh37.p13 chr11: 36,038,214-36,038,214 LDLRAD3
    nsv5710652mobile element insertion2nstd211human GRCh38 chr11: 35,986,040-35,986,040 , GRCh37.p13 chr11: 36,007,590-36,007,590 LDLRAD3
    nsv5701711mobile element insertion1nstd211human GRCh38 chr11: 36,023,169-36,023,169 , GRCh37.p13 chr11: 36,044,719-36,044,719 LDLRAD3
    nsv5700398mobile element insertion2nstd211human GRCh38 chr11: 36,152,060-36,152,060 , GRCh37.p13 chr11: 36,173,610-36,173,610 LDLRAD3
    nsv5698292mobile element insertion2nstd211human GRCh38 chr11: 36,161,722-36,161,722 , GRCh37.p13 chr11: 36,183,272-36,183,272 LDLRAD3
    nsv5697925mobile element insertion2nstd211human GRCh38 chr11: 36,039,497-36,039,497 , GRCh37.p13 chr11: 36,061,047-36,061,047 LDLRAD3
    nsv5662321insertion1nstd207human GRCh38 chr11: 35,986,025-35,986,025 , GRCh37.p13 chr11: 36,007,575-36,007,575 LDLRAD3
    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