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 124

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075103inversion1nstd229human GRCh38 chr20: 48,844,229-55,780,453 , GRCh37.p13 chr20: 47,460,766-54,355,509 RPL12P4, LOC105372664, 113 more genes
    nsv7065344inversion1nstd229human GRCh38 chr20: 49,128,244-52,291,086 , GRCh37.p13 chr20: 47,744,781-50,907,625 PARD6B, LOC105372657, 77 more genes
    nsv7064075inversion1nstd229human GRCh38 chr20: 49,009,324-55,851,498 , GRCh37.p13 chr20: 47,625,861-54,426,554 DPM1, KCNG1, 115 more genes
    nsv7037036copy number variation1nstd229human GRCh38 chr20: 50,273,053-50,281,311 , GRCh37.p13 chr20: 48,889,590-48,897,848 PELATON
    nsv7035158copy number variation1nstd229human GRCh38 chr20: 50,264,036-50,287,928 , GRCh37.p13 chr20: 48,880,573-48,904,465 PELATON, LOC105372656
    nsv7031820copy number variation1nstd229human GRCh38 chr20: 50,174,538-50,554,492 , GRCh37.p13 chr20: 48,791,075-49,171,029 LINC01271, CEBPB-AS1, 10 more genes
    nsv7029192copy number variation1nstd229human GRCh38 chr20: 50,276,483-50,277,144 , GRCh37.p13 chr20: 48,893,020-48,893,681 PELATON
    nsv7023693copy number variation1nstd229human GRCh38 chr20: 50,208,701-50,330,700 , GRCh37.p13 chr20: 48,825,238-48,947,237 PELATON, LINC01271, 3 more genes
    nsv7023419copy number variation1nstd229human GRCh38 chr20: 50,276,722-50,277,352 , GRCh37.p13 chr20: 48,893,259-48,893,889 PELATON
    nsv7020409copy number variation1nstd229human GRCh38 chr20: 49,428,501-51,120,300 , GRCh37.p13 chr20: 48,045,038-49,736,837 LOC100421569, RNU6-147P, 54 more genes
    nsv6544992copy number variation1nstd223human GRCh38 chr20: 50,273,053-50,281,306 , GRCh37.p13 chr20: 48,889,590-48,897,843 PELATON
    nsv6134303copy number variation1nstd213human GRCh37 chr20: 48,330,000-49,920,001 , GRCh38.p12 chr20: 49,713,463-51,303,464 KCNG1, PTPN1, 51 more genes
    nsv5013022copy number variation1nstd200human GRCh38 chr20: 50,276,552-50,277,190 , GRCh37.p13 chr20: 48,893,089-48,893,727 PELATON
    nsv5013021copy number variation1nstd200human GRCh38 chr20: 50,267,242-50,267,492 , GRCh37.p13 chr20: 48,883,779-48,884,029 PELATON
    nsv4853798copy number variation1nstd200human GRCh37 chr20: 48,893,089-48,893,727 , GRCh38.p12 chr20: 50,276,552-50,277,190 PELATON
    nsv4281264copy number variation1nstd166human GRCh37.p13 chr20: 48,893,089-48,893,727 , GRCh38.p12 chr20: 50,276,552-50,277,190 PELATON
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
    nsv3918469copy number variation1nstd102humanLikely pathogenic NCBI36 chr20: 48,039,067-49,545,590 , GRCh37 chr20: 48,605,660-50,112,183 , GRCh38 chr20: 49,989,123-51,495,645 CEBPB, KCNG1, 40 more genes
    nsv3916972copy number variation1nstd102humanPathogenic GRCh38 chr20: 49,947,237-55,875,406 , NCBI36 chr20: 47,997,181-53,883,869 , GRCh37 chr20: 48,563,774-54,450,462 UBE2V1, KRT18P4, 87 more genes
    nsv3915867copy number variation1nstd102humanPathogenic GRCh37 chr20: 48,347,613-49,819,103 , GRCh38 chr20: 49,731,076-51,202,566 , NCBI36 chr20: 47,781,020-49,252,510 PEDS1-UBE2V1, SLC9A8, 48 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