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 116

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7046389inversion1nstd229human GRCh38 chr1: 31,492,639-36,569,102 , GRCh37.p13 chr1: 32,017,064-37,034,703 LOC105378642, TMEM35B, 127 more genes
    nsv7044103inversion1nstd229human GRCh38 chr1: 26,905,652-33,050,814 , GRCh37.p13 chr1: 27,232,143-33,516,415 ADGRB2, SNORA16A, 169 more genes
    nsv6648890copy number variation1nstd229human GRCh38 chr1: 32,213,058-32,236,788 , GRCh37.p13 chr1: 32,678,659-32,702,389 DCDC2B, MTMR9LP, 2 more genes
    nsv6648746copy number variation1nstd229human GRCh38 chr1: 32,206,325-32,209,625 , GRCh37.p13 chr1: 32,671,926-32,675,226 TMEM234, IQCC, 1 more genes
    nsv6648745copy number variation1nstd229human GRCh38 chr1: 32,206,124-32,208,443 , GRCh37.p13 chr1: 32,671,725-32,674,044 IQCC, DCDC2B, 1 more genes
    nsv6330953copy number variation1nstd223human GRCh38 chr1: 32,206,122-32,208,442 , GRCh37.p13 chr1: 32,671,723-32,674,043 DCDC2B, IQCC, 1 more genes
    nsv6329842copy number variation1nstd223human GRCh38 chr1: 32,203,042-32,203,366 , GRCh37.p13 chr1: 32,668,643-32,668,967 TMEM234, CCDC28B
    nsv6327578copy number variation1nstd223human GRCh38 chr1: 32,213,336-32,219,559 , GRCh37.p13 chr1: 32,678,937-32,685,160 DCDC2B, TMEM234
    nsv6313817copy number variation1nstd102humanUncertain significance GRCh37 chr1: 32,462,251-32,721,488 , GRCh38.p12 chr1: 31,996,650-32,255,887 DCDC2B, TXLNA, 11 more genes
    nsv6313753copy number variation1nstd102humanUncertain significance GRCh37 chr1: 27,543,877-32,819,121 , GRCh38.p12 chr1: 27,217,386-32,353,520 DCDC2B, SNRNP40, 130 more genes
    nsv6133773copy number variation1nstd213human GRCh37 chr1: 31,350,000-33,290,001 , GRCh38.p12 chr1: 30,877,153-32,824,400 ADGRB2, COL16A1, 62 more genes
    nsv5983586copy number variation1nstd212human GRCh38 chr1: 30,209,364-32,642,526 , GRCh37.p13 chr1: 30,682,211-33,108,127 , HDAC1, 69 more genes
    nsv5428746copy number variation1nstd206human GRCh38 chr1: 32,206,122-32,208,442 , GRCh37.p13 chr1: 32,671,723-32,674,043 IQCC, TMEM234, 1 more genes
    nsv5424896copy number variation1nstd206human GRCh38 chr1: 32,203,042-32,203,366 , GRCh37.p13 chr1: 32,668,643-32,668,967 TMEM234, CCDC28B
    nsv5361103translocation1nstd200human GRCh38 chr1: 32,206,122-32,206,122 , GRCh38 chr1: 32,208,442-32,208,442 , GRCh37.p13 chr1: 32,674,043-32,674,043 , GRCh37.p13 chr1: 32,671,723-32,671,723 IQCC, TMEM234, 1 more genes
    nsv5078622mobile element insertion1nstd203human GRCh38 chr1: 32,213,445-32,213,462 , GRCh37.p13 chr1: 32,679,046-32,679,063 TMEM234, DCDC2B
    nsv4895809copy number variation1nstd200human GRCh38 chr1: 32,202,732-32,205,311 , GRCh37.p13 chr1: 32,668,333-32,670,912 CCDC28B, TMEM234, 1 more genes
    nsv4772963copy number variation1nstd200human GRCh37 chr1: 32,671,723-32,674,043 , GRCh38.p12 chr1: 32,206,122-32,208,442 TMEM234, IQCC, 1 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 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