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 231

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935302copy number variation1nstd209human GRCh38 chr17: 81,125,581-81,125,720 , GRCh37.p13 chr17: 79,099,381-79,099,520 AATK, MIR338, 2 more genes
    nsv5298108copy number variation1nstd204human GRCh38.p13 chr17: 80,930,501-82,586,000 , GRCh37.p13 chr17: 78,904,301-80,543,876 , PPP1R27, 89 more genes
    nsv5294695copy number variation1nstd204human GRCh38.p13 chr17: 80,930,501-81,587,000 , GRCh37.p13 chr17: 78,904,301-79,554,026 , LOC105371926, 32 more genes
    nsv4727905copy number variation1nstd197human GRCh37 chr17: 79,098,731-79,105,005 , GRCh38.p12 chr17: 81,124,931-81,131,205 AATK, MIR338, 3 more genes
    nsv4627176copy number variation1nstd183human GRCh37 chr17: 78,962,881-79,256,257 , GRCh38.p12 chr17: 80,989,081-81,282,457 , SLC38A10, 14 more genes
    nsv4626333copy number variation1nstd183human GRCh37 chr17: 79,047,113-79,109,909 , GRCh38.p12 chr17: 81,073,313-81,136,109 , AATK, 5 more genes
    nsv4625921copy number variation1nstd183human GRCh37 chr17: 78,632,841-79,703,517 , GRCh38.p12 chr17: 80,659,041-81,736,487 , HGS, 44 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4457483copy number variation1nstd102humanPathogenic GRCh37 chr17: 78,608,912-81,041,938 , GRCh38.p12 chr17: 80,635,112-83,084,062 HEXD, LOC105371929, 94 more genes
    nsv3919635copy number variation1nstd102humanPathogenic GRCh37 chr17: 76,088,317-81,044,553 , NCBI36 chr17: 73,599,912-78,637,842 , GRCh38 chr17: 78,092,236-83,086,677 LINC03048, MIR3186, 154 more genes
    nsv3919156copy number variation1nstd102humanPathogenic GRCh38 chr17: 69,916,435-83,102,552 , GRCh37 chr17: 67,912,576-81,048,189 , NCBI36 chr17: 65,424,171-78,653,717 CD300A, RNF213, 359 more genes
    nsv3917654copy number variation1nstd102humanPathogenic NCBI36 chr17: 64,716,815-78,637,842 , GRCh37 chr17: 67,205,220-81,044,553 , GRCh38 chr17: 69,209,079-83,086,677 LOC101928447, GRB2, 368 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
    nsv3914738copy number variation1nstd102humanPathogenic NCBI36 chr17: 74,409,636-78,637,842 , GRCh37 chr17: 76,898,041-81,044,553 , GRCh38 chr17: 78,901,959-83,086,677 MIR338, DUS1L, 127 more genes
    nsv3913720copy number variation1nstd102humanPathogenic GRCh38 chr17: 81,008,196-83,102,584 , GRCh37 chr17: 78,981,996-81,048,189 , NCBI36 chr17: 76,596,591-78,653,749 LOC105376789, MIR4525, 89 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
    nsv3911388copy number variation1nstd102humanPathogenic GRCh37 chr17: 76,914,732-80,978,971 , NCBI36 chr17: 74,426,327-78,572,260 , GRCh38 chr17: 78,918,650-83,021,095 ANAPC11, GPS1, 125 more genes
    nsv3909523copy number variation1nstd102humanPathogenic GRCh37 chr17: 63,689,671-81,041,938 , GRCh38.p12 chr17: 65,693,553-83,084,062 RPL38, RNF157-AS1, 428 more genes
    nsv3909511copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846 FOXK2, SOCS3-DT, 958 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