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 156

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5706102mobile element insertion2nstd211human GRCh38 chr15: 90,964,822-90,964,822 , GRCh37.p13 chr15: 91,508,052-91,508,052 PRC1, RCCD1, 1 more genes
    nsv5380768copy number variation1nstd102humanUncertain significance GRCh37 chr15: 91,290,623-91,512,067 , GRCh38.p12 chr15: 90,747,393-90,968,837 BLM, MAN2A2, 9 more genes
    nsv5349287translocation1nstd200human GRCh38 chr15: 90,957,094-90,957,094 , GRCh38 chr15: 90,957,216-90,957,216 , GRCh37.p13 chr15: 91,500,324-91,500,324 , GRCh37.p13 chr15: 91,500,446-91,500,446 RCCD1
    nsv5143167mobile element insertion1nstd203human GRCh38 chr15: 90,964,822-90,964,858 , GRCh37.p13 chr15: 91,508,052-91,508,088 PRC1, RCCD1, 1 more genes
    nsv5009181copy number variation1nstd200human GRCh38 chr15: 90,949,020-91,019,180 , GRCh37.p13 chr15: 91,492,250-91,562,410 UNC45A, PRC1, 4 more genes
    nsv5002375copy number variation1nstd200human GRCh38 chr15: 90,958,550-90,965,807 , GRCh37.p13 chr15: 91,501,780-91,509,037 RCCD1, PRC1-AS1, 1 more genes
    nsv5002374copy number variation1nstd200human GRCh38 chr15: 90,946,029-90,958,116 , GRCh37.p13 chr15: 91,489,259-91,501,346 RCCD1, UNC45A
    nsv5002373copy number variation1nstd200human GRCh38 chr15: 90,944,368-90,978,695 , GRCh37.p13 chr15: 91,487,598-91,521,925 RCCD1, PRC1-AS1, 2 more genes
    nsv5002372copy number variation1nstd200human GRCh38 chr15: 90,944,276-90,954,497 , GRCh37.p13 chr15: 91,487,506-91,497,727 UNC45A, RCCD1
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4681314copy number variation1nstd102humanUncertain significance GRCh37 chr15: 91,326,042-91,512,067 , GRCh38.p12 chr15: 90,782,812-90,968,837 MAN2A2, UNC45A, 9 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
    nsv4577711mobile element insertion1nstd166human GRCh37.p13 chr15: 91,497,679-91,497,679 , GRCh38.p12 chr15: 90,954,449-90,954,449 UNC45A, RCCD1
    nsv4457347copy number variation1nstd102humanUncertain significance GRCh37 chr15: 91,276,782-91,550,953 , GRCh38.p12 chr15: 90,733,551-91,007,723 BLM, MAN2A2, 10 more genes
    nsv4456778copy number variation1nstd102humanPathogenic GRCh37 chr15: 91,229,877-93,677,014 , GRCh38.p12 chr15: 90,686,646-93,133,785 H2AZ2P1, MAN2A2, 44 more genes
    nsv4456430copy number variation1nstd102humanPathogenic GRCh37 chr15: 90,288,175-102,429,112 , GRCh38.p12 chr15: 89,744,944-101,888,909 IQGAP1, LOC400464, 210 more genes
    nsv4377776copy number variation1nstd173human GRCh37 chr15: 86,980,083-93,499,239 , GRCh38.p12 chr15: 86,436,852-92,956,009 , RNU6-1111P, 136 more genes
    nsv4350274copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,883,823-92,165,844 , GRCh38.p12 chr15: 83,215,071-91,622,614 AKAP13, LOC105370972, 184 more genes
    nsv4240181copy number variation1nstd166human GRCh37.p13 chr15: 91,496,000-91,501,000 , GRCh38.p12 chr15: 90,952,770-90,957,770 UNC45A, RCCD1
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    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