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 108

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048973inversion1nstd229human GRCh38 chr2: 85,313,337-85,343,180 , GRCh37.p13 chr2: 85,540,460-85,570,303 PEBP1P2, TGOLN2, 1 more genes
    nsv6681244copy number variation1nstd229human GRCh38 chr2: 85,286,438-85,844,313 , GRCh37.p13 chr2: 85,513,561-86,071,436 RETSAT, SH2D6, 30 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6550543inversion1nstd223human GRCh38 chr2: 85,315,940-85,343,854 , GRCh37.p13 chr2: 85,543,063-85,570,977 TGOLN2, RETSAT, 1 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313890copy number variation1nstd102humanPathogenic GRCh37 chr2: 82,486,900-87,322,042 , GRCh38.p12 chr2: 82,259,776-87,094,919 LOC105374836, LOC105374833, 93 more genes
    nsv6112750copy number variation1nstd102humanPathogenic GRCh37 chr2: 81,209,244-86,688,030 , GRCh38.p12 chr2: 80,982,120-86,460,907 VAMP8, TMSB10, 86 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4902361copy number variation1nstd200human GRCh38 chr2: 85,335,895-85,339,382 , GRCh37.p13 chr2: 85,563,018-85,566,505 PEBP1P2
    nsv4902360copy number variation1nstd200human GRCh38 chr2: 85,332,431-85,339,382 , GRCh37.p13 chr2: 85,559,554-85,566,505 PEBP1P2
    nsv4674314copy number variation1nstd102humanUncertain significance GRCh37 chr2: 85,401,388-85,615,492 , GRCh38.p12 chr2: 85,174,265-85,388,369 TCF7L1, TCF7L1-IT1, 8 more genes
    nsv4673943copy number variation1nstd102humanUncertain significance GRCh37 chr2: 85,357,332-85,685,465 , GRCh38.p12 chr2: 85,130,209-85,458,342 SNRPEP11, PEBP1P2, 13 more genes
    nsv4595820copy number variation1nstd183human GRCh37 chr2: 85,505,867-85,911,446 , GRCh38.p12 chr2: 85,278,744-85,684,323 , RN7SL251P, 23 more genes
    nsv4586725copy number variation1nstd183human GRCh37 chr2: 85,565,621-85,571,466 , GRCh38.p12 chr2: 85,338,498-85,344,343 RETSAT, PEBP1P2
    nsv4584593copy number variation1nstd183human GRCh37 chr2: 85,508,825-85,911,677 , GRCh38.p12 chr2: 85,281,702-85,684,554 , USP39, 24 more genes
    nsv4451607copy number variation1nstd102humanPathogenic GRCh37 chr2: 77,907,114-87,330,965 , GRCh38.p12 chr2: 77,679,988-87,103,842 REEP1, RBX1P1, 134 more genes
    nsv3958451copy number variation1nstd168human GRCh38 chr2: 85,281,876-85,355,655 , GRCh37.p13 chr2: 85,508,999-85,582,778 , TGOLN2, 4 more genes
    nsv3916821copy number variation1nstd102humanPathogenic NCBI36 chr2: 47,701,031-86,783,356 , GRCh37.p13 chr2: 47,847,527-86,929,845 , GRCh38.p12 chr2: 47,620,388-86,702,722 NAGK, NRXN1-DT, 595 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