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 849

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117669copy number variation1nstd186human GRCh37 chrX: 1,527,470-1,529,138 , GRCh38.p12 chrX: 1,408,577-1,410,245 ASMTL, ASMTL-AS1
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5979356copy number variation1nstd209human GRCh38 chrX: 1,407,572-1,414,841 , GRCh37.p13 chrX: 1,526,465-1,533,734 ASMTL-AS1, ASMTL
    nsv5973645copy number variation1nstd209human GRCh38 chrX: 1,391,092-1,400,080 , GRCh37.p13 chrX: 1,509,985-1,518,973 , SLC25A6, 2 more genes
    nsv5973547copy number variation1nstd209human GRCh38 chrX: 1,408,041-1,419,851 , GRCh37.p13 chrX: 1,526,934-1,538,744 ASMTL-AS1, ASMTL
    nsv5972301copy number variation1nstd209human GRCh38 chrX: 1,412,842-1,429,344 , GRCh37.p13 chrX: 1,531,735-1,548,237 ASMTL-AS1, ASMTL
    nsv5971648copy number variation1nstd209human GRCh38 chrX: 1,408,040-1,429,344 , GRCh37.p13 chrX: 1,526,933-1,548,237 ASMTL, ASMTL-AS1
    nsv5971507copy number variation2nstd209human GRCh38 chrX: 1,399,481-1,400,929 , GRCh37.p13 chrX: 1,518,374-1,519,822 LINC00106, ASMTL-AS1
    nsv5971296copy number variation1nstd209human GRCh38 chrX: 1,408,039-1,422,606 , GRCh37.p13 chrX: 1,526,932-1,541,499 ASMTL-AS1, ASMTL
    nsv5884902copy number variation1nstd209human GRCh38 chrX: 1,408,032-1,410,310 , GRCh37.p13 chrX: 1,526,925-1,529,203 ASMTL, ASMTL-AS1
    nsv5883590copy number variation1nstd209human GRCh38 chrX: 1,405,176-1,406,336 , GRCh37.p13 chrX: 1,524,069-1,525,229 ASMTL, ASMTL-AS1
    nsv5879447copy number variation1nstd209human GRCh38 chrX: 1,410,351-1,410,834 , GRCh37.p13 chrX: 1,529,244-1,529,727 ASMTL, ASMTL-AS1
    nsv5879300copy number variation1nstd209human GRCh38 chrX: 1,407,375-1,407,530 , GRCh37.p13 chrX: 1,526,268-1,526,423 ASMTL-AS1, ASMTL
    nsv5879057copy number variation1nstd209human GRCh38 chrX: 1,405,187-1,406,770 , GRCh37.p13 chrX: 1,524,080-1,525,663 ASMTL, ASMTL-AS1
    nsv5878863copy number variation1nstd209human GRCh38 chrX: 1,405,746-1,406,160 , GRCh37.p13 chrX: 1,524,639-1,525,053 ASMTL, ASMTL-AS1
    nsv5878794copy number variation1nstd209human GRCh38 chrX: 1,404,935-1,405,175 , GRCh37.p13 chrX: 1,523,828-1,524,068 ASMTL, ASMTL-AS1
    nsv5878779copy number variation1nstd209human GRCh38 chrX: 1,405,113-1,405,379 , GRCh37.p13 chrX: 1,524,006-1,524,272 ASMTL-AS1, ASMTL
    nsv5878556copy number variation1nstd209human GRCh38 chrX: 1,404,124-1,404,277 , GRCh37.p13 chrX: 1,523,017-1,523,170 ASMTL-AS1, ASMTL
    nsv5877872copy number variation1nstd209human GRCh38 chrX: 1,402,667-1,402,717 , GRCh37.p13 chrX: 1,521,560-1,521,610 ASMTL-AS1, ASMTL
    nsv5877482copy number variation1nstd209human GRCh38 chrX: 1,408,133-1,410,299 , GRCh37.p13 chrX: 1,527,026-1,529,192 ASMTL-AS1, ASMTL
    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