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 606

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146227copy number variation1nstd232human GRCh37.p13 chr1: 37,423,940-37,424,018 , GRCh38.p12 chr1: 36,958,339-36,958,417 GRIK3
    nsv7140784insertion1nstd232human GRCh37.p13 chr1: 37,423,055-37,423,055 , GRCh38.p12 chr1: 36,957,454-36,957,454 GRIK3
    nsv7099193copy number variation1nstd231human GRCh38.p12 chr1: 32,456,017-38,905,781 , GRCh37 chr1: 32,921,618-39,371,453 AK2, COL8A2, 151 more genes
    nsv7053645inversion1nstd229human GRCh38 chr1: 36,820,346-36,820,417 , GRCh37.p13 chr1: 37,285,947-37,286,018 GRIK3
    nsv7050155inversion1nstd229human GRCh38 chr1: 36,919,220-36,919,302 , GRCh37.p13 chr1: 37,384,821-37,384,903 GRIK3
    nsv7049253inversion1nstd229human GRCh38 chr1: 37,026,897-37,035,625 , GRCh37.p13 chr1: 37,492,498-37,501,226 GRIK3
    nsv7048835inversion1nstd229human GRCh38 chr1: 36,883,155-36,883,167 , GRCh37.p13 chr1: 37,348,756-37,348,768 GRIK3
    nsv7047647inversion1nstd229human GRCh38 chr1: 36,863,898-36,863,910 , GRCh37.p13 chr1: 37,329,499-37,329,511 GRIK3
    nsv7046918inversion1nstd229human GRCh38 chr1: 34,689,928-38,980,899 , GRCh37.p13 chr1: 35,155,529-39,446,571 LOC105378647, NCDN, 112 more genes
    nsv7040332inversion1nstd229human GRCh38 chr1: 34,936,903-38,057,517 , GRCh37.p13 chr1: 35,402,504-38,523,189 MAP7D1, RPL12P45, 83 more genes
    nsv6649546copy number variation1nstd229human GRCh38 chr1: 37,030,283-37,032,406 , GRCh37.p13 chr1: 37,495,884-37,498,007 GRIK3
    nsv6649545copy number variation1nstd229human GRCh38 chr1: 37,029,079-37,029,129 , GRCh37.p13 chr1: 37,494,680-37,494,730 GRIK3
    nsv6649543copy number variation1nstd229human GRCh38 chr1: 36,966,509-36,966,693 , GRCh37.p13 chr1: 37,432,110-37,432,294 GRIK3
    nsv6649542copy number variation1nstd229human GRCh38 chr1: 36,964,935-36,974,827 , GRCh37.p13 chr1: 37,430,536-37,440,428 GRIK3
    nsv6649541copy number variation1nstd229human GRCh38 chr1: 36,958,638-36,960,147 , GRCh37.p13 chr1: 37,424,239-37,425,748 GRIK3
    nsv6649537copy number variation1nstd229human GRCh38 chr1: 36,886,072-36,886,254 , GRCh37.p13 chr1: 37,351,673-37,351,855 GRIK3
    nsv6649536copy number variation1nstd229human GRCh38 chr1: 36,830,451-36,837,622 , GRCh37.p13 chr1: 37,296,052-37,303,223 GRIK3
    nsv6649493copy number variation1nstd229human GRCh38 chr1: 36,951,669-36,956,489 , GRCh37.p13 chr1: 37,417,270-37,422,090 GRIK3
    nsv6649346copy number variation1nstd229human GRCh38 chr1: 36,965,601-36,973,600 , GRCh37.p13 chr1: 37,431,202-37,439,201 GRIK3
    nsv6649344copy number variation1nstd229human GRCh38 chr1: 36,958,501-36,960,400 , GRCh37.p13 chr1: 37,424,102-37,426,001 GRIK3
    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