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 287

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148184copy number variation1nstd102humanPathogenic GRCh38 chr1: 243,221,458-248,919,110 , GRCh37.p13 chr1: 243,384,760-249,213,309 LOC105373271, LOC107985725, 153 more genes
    nsv7099272copy number variation1nstd231human GRCh38.p12 chr1: 243,197,153-248,437,482 , GRCh37 chr1: 243,360,455-248,600,783 ADSS2, HNRNPU, 124 more genes
    nsv7098854copy number variation1nstd102humanPathogenic GRCh37 chr1: 245,704,069-249,212,562 , GRCh38.p12 chr1: 245,540,767-248,918,363 OR2X1P, OR14A2, 118 more genes
    nsv7055426inversion1nstd229human GRCh38 chr1: 247,429,281-247,845,194 , GRCh37.p13 chr1: 247,592,583-248,008,496 OR14L1, OR6R1P, 19 more genes
    nsv7049735inversion1nstd229human GRCh38 chr1: 247,664,727-247,954,522 , GRCh37.p13 chr1: 247,828,029-248,117,824 OR2T8, OR6F1, 17 more genes
    nsv7049548inversion1nstd229human GRCh38 chr1: 247,434,792-247,854,366 , GRCh37.p13 chr1: 247,598,094-248,017,668 OR2G2, LOC102724446, 19 more genes
    nsv7041671inversion1nstd229human GRCh38 chr1: 247,239,306-248,299,501 , GRCh37.p13 chr1: 247,402,608-248,462,803 OR9H1P, OR2L9P, 49 more genes
    nsv7040948inversion1nstd229human GRCh38 chr1: 247,397,103-247,762,133 , GRCh37.p13 chr1: 247,560,405-247,925,435 OR2G3, OR2W5P, 14 more genes
    nsv6675891copy number variation1nstd229human GRCh38 chr1: 247,670,360-247,671,016 , GRCh37.p13 chr1: 247,833,662-247,834,318 OR13G1
    nsv6673925copy number variation1nstd229human GRCh38 chr1: 247,506,357-247,841,446 , GRCh37.p13 chr1: 247,669,659-248,004,748 OR14A2, OR14L1, 16 more genes
    nsv6667957copy number variation1nstd229human GRCh38 chr1: 247,515,980-247,913,359 , GRCh37.p13 chr1: 247,679,282-248,076,661 OR2C3, OR6F1, 18 more genes
    nsv6667436copy number variation1nstd229human GRCh38 chr1: 247,621,169-247,828,347 , GRCh37.p13 chr1: 247,784,471-247,991,649 OR3D1P, OR14A2, 8 more genes
    nsv6665900copy number variation1nstd229human GRCh38 chr1: 247,656,440-248,785,565 , GRCh37.p13 chr1: 247,819,742-248,865,778 OR2X1P, OR3D1P, 60 more genes
    nsv6660649copy number variation1nstd229human GRCh38 chr1: 247,644,151-247,762,171 , GRCh37.p13 chr1: 247,807,453-247,925,473 OR1C1, OR14A2, 4 more genes
    nsv6659533copy number variation1nstd229human GRCh38 chr1: 247,373,080-248,325,181 , GRCh37.p13 chr1: 247,536,382-248,488,483 OR2L3, OR2L5, 47 more genes
    nsv6659249copy number variation1nstd229human GRCh38 chr1: 247,556,814-248,422,746 , GRCh37.p13 chr1: 247,720,116-248,586,047 OR2L13, TRIM58, 44 more genes
    nsv6637119copy number variation1nstd102humanUncertain significance GRCh37 chr1: 247,671,905-247,981,897 , GRCh38.p12 chr1: 247,508,603-247,818,595 OR14K1, OR13G1, 13 more genes
    nsv6637024copy number variation1nstd102humanUncertain significance GRCh37 chr1: 247,588,318-248,022,379 , GRCh38.p12 chr1: 247,425,016-247,859,077 OR14L1, OR11L1, 20 more genes
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
    nsv6636648copy number variation1nstd102humanPathogenic GRCh37 chr1: 239,910,960-249,224,684 , GRCh38.p12 chr1: 239,747,660-248,930,485 RFKP1, OR2T29, 206 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