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 410

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5941972copy number variation1nstd209human GRCh38 chr17: 18,975,562-18,976,056 , GRCh37.p13 chr17: 18,878,875-18,879,369 FAM83G, SLC5A10
    nsv5933579copy number variation1nstd209human GRCh38 chr17: 16,936,959-20,558,118 , GRCh37.p13 chr17: 16,840,273-20,461,431 , FAM106B, 146 more genes
    nsv5883902copy number variation1nstd209human GRCh38 chr17: 18,986,571-18,988,270 , GRCh37.p13 chr17: 18,889,884-18,891,583 FAM83G, SLC5A10
    nsv5883686copy number variation1nstd209human GRCh38 chr17: 18,995,315-18,996,645 , GRCh37.p13 chr17: 18,898,628-18,899,958 FAM83G, SLC5A10
    nsv5873977copy number variation1nstd209human GRCh38 chr17: 18,968,546-19,013,149 , GRCh37.p13 chr17: 18,871,859-18,916,462 SLC5A10, FAM83G
    nsv5532475copy number variation1nstd206human GRCh38 chr17: 18,991,511-18,991,573 , GRCh37.p13 chr17: 18,894,824-18,894,886 SLC5A10, FAM83G
    nsv5521643copy number variation1nstd206human GRCh38 chr17: 18,964,536-18,966,799 , GRCh37.p13 chr17: 18,867,849-18,870,112 FAM83G, SLC5A10
    nsv5519170copy number variation1nstd206human GRCh38 chr17: 18,920,402-19,018,426 , GRCh37.p13 chr17: 18,823,715-18,921,739 SLC5A10, PRPSAP2, 1 more genes
    nsv5518024copy number variation1nstd206human GRCh38 chr17: 19,006,234-19,006,537 , GRCh37.p13 chr17: 18,909,547-18,909,850 FAM83G, SLC5A10
    nsv5381800copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,601,603-20,063,369 , GRCh38.p12 chr17: 16,698,289-20,160,056 COTL1P1, LOC105371551, 141 more genes
    nsv5381797copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,145,361-20,137,943 , GRCh38.p12 chr17: 17,242,047-20,234,630 LOC644909, FLII, 117 more genes
    nsv5358692translocation1nstd200human GRCh38 chr17: 18,990,335-18,990,335 , GRCh38 chr17: 18,992,390-18,992,390 , GRCh37.p13 chr17: 18,895,703-18,895,703 , GRCh37.p13 chr17: 18,893,648-18,893,648 FAM83G, SLC5A10
    nsv5328852copy number variation1nstd204human GRCh37.p13 chr17: 18,892,164-18,894,436 , GRCh38.p13 chr17: 18,988,851-18,991,123 SLC5A10, FAM83G
    nsv5325511copy number variation1nstd204human GRCh38.p13 chr17: 18,920,379-19,018,455 , GRCh37.p13 chr17: 18,823,692-18,921,768 PRPSAP2, SLC5A10, 1 more genes
    nsv5325233copy number variation1nstd204human GRCh38.p13 chr17: 18,964,569-18,966,819 , GRCh37.p13 chr17: 18,867,882-18,870,132 SLC5A10, FAM83G
    nsv5297134copy number variation1nstd204human GRCh38.p13 chr17: 18,920,401-19,017,300 , GRCh37.p13 chr17: 18,823,714-18,920,613 FAM83G, PRPSAP2, 1 more genes
    nsv5284693copy number variation1nstd204human GRCh38.p13 chr17: 18,964,933-18,966,932 , GRCh37.p13 chr17: 18,868,246-18,870,245 FAM83G, SLC5A10
    nsv5196841mobile element insertion1nstd203human GRCh38 chr17: 18,975,695-18,975,695 , GRCh37.p13 chr17: 18,879,008-18,879,008 SLC5A10, FAM83G
    nsv5026173copy number variation1nstd200human GRCh38 chr17: 19,000,296-19,003,869 , GRCh37.p13 chr17: 18,903,609-18,907,182 FAM83G, SLC5A10
    nsv5023741copy number variation1nstd200human GRCh38 chr17: 18,920,402-19,018,426 , GRCh37.p13 chr17: 18,823,715-18,921,739 FAM83G, SLC5A10, 1 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