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 192

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5933295copy number variation1nstd209human GRCh38 chr17: 54,955,603-54,956,728 , GRCh37.p13 chr17: 53,032,964-53,034,089 COX11, TOM1L1
    nsv5883999copy number variation1nstd209human GRCh38 chr17: 54,955,565-54,957,064 , GRCh37.p13 chr17: 53,032,926-53,034,425 TOM1L1, COX11
    nsv5724105mobile element insertion1nstd211human GRCh38 chr17: 54,963,822-54,963,822 , GRCh37.p13 chr17: 53,041,183-53,041,183 COX11
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5530843copy number variation1nstd206human GRCh38 chr17: 54,955,699-54,958,830 , GRCh37.p13 chr17: 53,033,060-53,036,191 TOM1L1, COX11
    nsv5529332copy number variation1nstd206human GRCh38 chr17: 54,631,610-54,997,284 , GRCh37.p13 chr17: 52,708,971-53,074,645 , COX11, 4 more genes
    nsv5358977translocation1nstd200human GRCh38 chr17: 54,955,607-54,955,607 , GRCh38 chr17: 54,956,729-54,956,729 , GRCh37.p13 chr17: 53,032,968-53,032,968 , GRCh37.p13 chr17: 53,034,090-53,034,090 TOM1L1, COX11
    nsv5026549copy number variation1nstd200human GRCh38 chr17: 54,967,524-54,968,828 , GRCh37.p13 chr17: 53,044,885-53,046,189 COX11, STXBP4
    nsv5026545copy number variation1nstd200human GRCh38 chr17: 54,818,935-54,992,286 , GRCh37.p13 chr17: 52,896,296-53,069,647 , STXBP4, 2 more genes
    nsv4864724copy number variation1nstd200human GRCh37 chr17: 53,044,050-53,044,194 , GRCh38.p12 chr17: 54,966,689-54,966,833 COX11, STXBP4
    nsv4629834copy number variation1nstd183human GRCh37 chr17: 53,040,283-53,042,068 , GRCh38.p12 chr17: 54,962,922-54,964,707 COX11
    nsv4620968copy number variation1nstd183human GRCh37 chr17: 53,040,283-53,040,682 , GRCh38.p12 chr17: 54,962,922-54,963,321 COX11
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4264040copy number variation1nstd166human GRCh37.p13 chr17: 53,032,968-53,034,090 , GRCh38.p12 chr17: 54,955,607-54,956,729 TOM1L1, COX11
    nsv3920880copy number variation1nstd102humanPathogenic GRCh38 chr17: 49,974,533-56,807,609 , NCBI36 chr17: 45,406,896-52,239,969 , GRCh37 chr17: 48,051,897-54,884,970 LOC107984983, LOC102724732, 85 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
    nsv3913183copy number variation1nstd102humanUncertain significance NCBI36 chr17: 50,062,202-50,431,571 , GRCh37.p13 chr17: 52,707,203-53,076,572 , GRCh38.p12 chr17: 54,629,842-54,999,211 COX11, TOM1L1, 3 more genes
    nsv3911903copy number variation1nstd102humanBenign NCBI36 chr17: 49,937,240-50,396,464 , GRCh37 chr17: 52,582,241-53,041,465 , GRCh38 chr17: 54,504,880-54,964,104 RN7SKP14, TOM1L1, 2 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 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