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 150

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5702022mobile element insertion2nstd211human GRCh38 chr17: 14,063,869-14,063,869 , GRCh37.p13 chr17: 13,967,186-13,967,186 COX10-DT
    nsv5695293mobile element insertion1nstd211human GRCh38 chr17: 14,047,029-14,047,029 , GRCh37.p13 chr17: 13,950,346-13,950,346 COX10-DT
    nsv5525414copy number variation1nstd206human GRCh38 chr17: 14,053,741-14,130,426 , GRCh37.p13 chr17: 13,957,058-14,033,743 COX10-DT, COX10
    nsv5521683copy number variation1nstd206human GRCh38 chr17: 14,033,891-14,151,767 , GRCh37.p13 chr17: 13,937,208-14,055,084 COX10-DT, COX10
    nsv5520330copy number variation1nstd206human GRCh38 chr17: 14,022,600-15,889,111 , GRCh37.p13 chr17: 13,925,917-15,792,425 CDRT15, CDRT7, 42 more genes
    nsv5430380mobile element insertion1nstd206human GRCh38 chr17: 14,063,869-14,063,872 , GRCh37.p13 chr17: 13,967,186-13,967,189 COX10-DT
    nsv5414012mobile element insertion1nstd206human GRCh38 chr17: 14,047,029-14,047,080 , GRCh37.p13 chr17: 13,950,346-13,950,397 COX10-DT
    nsv5365742translocation1nstd200human GRCh38 chr17: 14,064,138-14,064,138 , GRCh38 chr17: 14,061,175-14,061,175 , GRCh37.p13 chr17: 13,967,455-13,967,455 , GRCh37.p13 chr17: 13,964,492-13,964,492 COX10-DT
    nsv5358660translocation1nstd200human GRCh38 chr17: 14,064,145-14,064,145 , GRCh38 chr17: 14,061,380-14,061,380 , GRCh37.p13 chr17: 13,964,697-13,964,697 , GRCh37.p13 chr17: 13,967,462-13,967,462 COX10-DT
    nsv5145661mobile element insertion1nstd203human GRCh38 chr17: 14,037,785-14,037,800 , GRCh37.p13 chr17: 13,941,102-13,941,117 COX10-DT
    nsv5025957copy number variation1nstd200human GRCh38 chr17: 14,033,891-14,151,767 , GRCh37.p13 chr17: 13,937,208-14,055,084 COX10-DT, COX10
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4684245copy number variation1nstd102humanUncertain significance GRCh37 chr17: 10,493,837-15,099,023 , GRCh38.p12 chr17: 10,590,520-15,195,706 LOC100506974, MIR1269B, 52 more genes
    nsv4675628copy number variation1nstd102humanUncertain significance GRCh37 chr17: 13,933,395-14,055,324 , GRCh38.p12 chr17: 14,030,078-14,152,007 COX10-DT, COX10
    nsv4636776copy number variation1nstd186human GRCh37 chr17: 13,927,000-13,933,000 , GRCh38.p12 chr17: 14,023,683-14,029,683 CDRT15P1, COX10-DT
    nsv4626801copy number variation1nstd183human GRCh37 chr17: 13,945,658-14,099,126 , GRCh38.p12 chr17: 14,042,341-14,195,809 COX10, COX10-DT
    nsv4510218mobile element insertion1nstd166human GRCh37.p13 chr17: 13,941,102-13,941,102 , GRCh38.p12 chr17: 14,037,785-14,037,785 COX10-DT
    nsv4503320mobile element insertion1nstd166human GRCh37.p13 chr17: 13,948,163-13,948,163 , GRCh38.p12 chr17: 14,044,846-14,044,846 COX10-DT
    nsv4457482copy number variation1nstd102humanPathogenic GRCh37 chr17: 13,879,079-14,013,128 , GRCh38.p12 chr17: 13,975,762-14,109,811 CDRT15P1, COX10-DT, 1 more genes
    nsv4436354complex substitution1nstd102humanUncertain significance GRCh37 chr17: 9,586,165-16,325,968 , GRCh38.p12 chr17: 9,682,848-16,422,654 ADORA2B, COX10, 109 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center