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 159

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130159insertion1nstd186human GRCh37 chr17: 38,975,146-38,975,154 , GRCh38.p12 chr17: 40,818,894-40,818,902 KRT10, KRT10-AS1
    nsv5938451copy number variation1nstd209human GRCh38 chr17: 40,825,741-40,833,005 , GRCh37.p13 chr17: 38,981,993-38,989,257 KRT10-AS1
    nsv5867699copy number variation1nstd209human GRCh38 chr17: 40,825,729-40,833,034 , GRCh37.p13 chr17: 38,981,981-38,989,286 KRT10-AS1
    nsv5647947insertion1nstd207human GRCh38 chr17: 40,818,851-40,818,851 , GRCh37.p13 chr17: 38,975,103-38,975,103 KRT10-AS1, KRT10
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5537129insertion1nstd206human GRCh38 chr17: 40,818,894-40,818,902 , GRCh37.p13 chr17: 38,975,146-38,975,154 KRT10, KRT10-AS1
    nsv4757887insertion1nstd199human GRCh37 chr17: 38,975,121-38,975,121 , GRCh38.p12 chr17: 40,818,869-40,818,869 KRT10, KRT10-AS1
    nsv4679355copy number variation1nstd189human GRCh37.p13 chr17: 38,659,900-39,414,647 , GRCh38.p12 chr17: 40,503,648-41,258,395 , CCR7, 54 more genes
    nsv4622691copy number variation1nstd183human GRCh37 chr17: 38,974,412-38,974,918 , GRCh38.p12 chr17: 40,818,160-40,818,666 KRT10-AS1, KRT10
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4262659copy number variation1nstd166human GRCh37.p13 chr17: 38,992,030-39,067,708 , GRCh38.p12 chr17: 40,835,778-40,911,456 , GRCh38.p12 chr17|NW_003871091.1: 1-60,724 KRT12, KRT20, 2 more genes
    nsv4261517copy number variation1nstd166human GRCh37.p13 chr17: 38,975,221-38,975,329 , GRCh38.p12 chr17: 40,818,969-40,819,077 KRT10-AS1, KRT10
    nsv3924499delins1nstd102humanLikely benign GRCh37 chr17: 38,975,328-38,975,329 , GRCh38 chr17: 40,819,076-40,819,077 KRT10, KRT10-AS1
    nsv3914976delins1nstd102humanLikely benign GRCh37 chr17: 38,975,147-38,975,163 , GRCh38 chr17: 40,818,895-40,818,911 KRT10, KRT10-AS1
    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
    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
    nsv3911563copy number variation1nstd102humanPathogenic NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214 PLEKHH3, CHCT1, 958 more genes
    nsv3911344copy number variation1nstd102humanPathogenic GRCh37 chr17: 37,356,126-43,706,945 , NCBI36 chr17: 34,609,652-41,062,728 , GRCh38 chr17: 39,199,873-45,629,579 IFI35, RND2, 345 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 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