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 165

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5729067mobile element insertion1nstd211human GRCh38 chr1: 71,072,413-71,072,413 , GRCh37.p13 chr1: 71,538,096-71,538,096 ZRANB2
    nsv5725053mobile element insertion1nstd211human GRCh38 chr1: 71,072,424-71,072,424 , GRCh37.p13 chr1: 71,538,107-71,538,107 ZRANB2
    nsv5674453mobile element insertion1nstd211human GRCh38 chr1: 71,079,463-71,079,463 , GRCh37.p13 chr1: 71,545,146-71,545,146 ZRANB2, ZRANB2-DT
    nsv5561145mobile element insertion1nstd206human GRCh38 chr1: 71,072,427-71,072,475 , GRCh37.p13 chr1: 71,538,110-71,538,158 ZRANB2
    nsv5424562copy number variation1nstd206human GRCh38 chr1: 71,070,688-71,070,744 , GRCh37.p13 chr1: 71,536,371-71,536,427 ZRANB2
    nsv5419262copy number variation1nstd206human GRCh38 chr1: 71,074,701-71,076,444 , GRCh37.p13 chr1: 71,540,384-71,542,127 ZRANB2
    nsv5409059mobile element insertion1nstd206human GRCh38 chr1: 71,079,463-71,079,514 , GRCh37.p13 chr1: 71,545,146-71,545,197 ZRANB2, ZRANB2-DT
    nsv5175992mobile element insertion1nstd203human GRCh38 chr1: 71,072,418-71,072,427 , GRCh37.p13 chr1: 71,538,101-71,538,110 ZRANB2
    nsv5169675mobile element insertion1nstd203human GRCh38 chr1: 71,072,416-71,072,427 , GRCh37.p13 chr1: 71,538,099-71,538,110 ZRANB2
    nsv5161133mobile element insertion1nstd203human GRCh38 chr1: 71,072,413-71,072,427 , GRCh37.p13 chr1: 71,538,096-71,538,110 ZRANB2
    nsv4896220copy number variation1nstd200human GRCh38 chr1: 71,076,957-71,077,082 , GRCh37.p13 chr1: 71,542,640-71,542,765 ZRANB2
    nsv4896219copy number variation1nstd200human GRCh38 chr1: 71,074,701-71,076,444 , GRCh37.p13 chr1: 71,540,384-71,542,127 ZRANB2
    nsv4888344inversion1nstd200human GRCh37 chr1: 51,769,169-94,478,994 , GRCh38.p12 chr1: 51,303,497-94,013,438 , ST13P20, 664 more genes
    nsv4783664copy number variation1nstd200human GRCh37 chr1: 71,542,640-71,542,765 , GRCh38.p12 chr1: 71,076,957-71,077,082 ZRANB2
    nsv4783663copy number variation1nstd200human GRCh37 chr1: 71,540,384-71,542,127 , GRCh38.p12 chr1: 71,074,701-71,076,444 ZRANB2
    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
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4674361copy number variation1nstd102humanUncertain significance GRCh37 chr1: 71,419,650-72,398,325 , GRCh38.p12 chr1: 70,953,967-71,932,642 NEGR1-IT1, PTGER3, 6 more genes
    nsv4594642copy number variation1nstd183human GRCh37 chr1: 71,429,866-71,533,933 , GRCh38.p12 chr1: 70,964,183-71,068,250 , ZRANB2, 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