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 147

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5142075mobile element insertion1nstd203human GRCh38 chr17: 38,746,338-38,746,353 , GRCh37.p13 chr17: 36,902,591-36,902,606 PCGF2
    nsv5016243copy number variation1nstd200human GRCh38 chr17: 38,736,631-38,737,694 , GRCh37.p13 chr17: 36,892,884-36,893,947 PCGF2
    nsv4858733copy number variation1nstd200human GRCh37 chr17: 36,897,021-36,897,463 , GRCh38.p12 chr17: 38,740,768-38,741,210 , GRCh38.p12 chr17|NT_187614.1: 2,776,087-2,776,529 PCGF2
    nsv4675332copy number variation1nstd102humanUncertain significance GRCh37 chr17: 36,710,984-37,295,662 , GRCh38.p12 chr17: 38,600,767-39,139,409 PIP4K2B, PSMB3, 32 more genes
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4366314copy number variation1nstd173human GRCh37 chr17: 36,898,585-36,932,200 , GRCh38.p12 chr17: 38,742,332-38,775,947 , GRCh38.p12 chr17|NT_187614.1: 2,777,651-2,811,266 PCGF2, RNU6-866P, 4 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 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
    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
    nsv3908326copy number variation1nstd102humanBenign GRCh37 chr17: 36,906,480-36,996,181 , GRCh38.p12 chr17: 38,750,227-38,839,928 , GRCh38.p12 chr17|NT_187614.1: 2,785,546-2,875,247 PCGF2, SPMAP1, 7 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 MIR21, LOC105371899, 2366 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 MIR3185, YWHAEP6, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 P4HB, LOC105371808, 2366 more genes
    nsv3892646copy number variation1nstd102humanUncertain significance GRCh37 chr17: 36,891,708-36,909,570 , GRCh38.p12 chr17: 38,735,455-38,753,317 , GRCh38.p12 chr17|NT_187614.1: 2,770,774-2,788,636 TRN-GTT2-5, PCGF2, 4 more genes
    nsv3892633copy number variation1nstd102humanLikely benign GRCh37 chr17: 36,891,708-36,912,092 , GRCh38.p12 chr17: 38,735,455-38,755,839 , GRCh38.p12 chr17|NT_187614.1: 2,770,774-2,791,158 PCGF2, PSMB3, 4 more genes
    nsv3163577copy number variation1nstd151human GRCh37 chr17: 36,894,603-36,909,592 , GRCh38.p12 chr17: 38,738,350-38,753,339 , GRCh38.p12 chr17|NT_187614.1: 2,773,669-2,788,658 LOC100287808, PSMB3, 3 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