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
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5971709insertion1nstd209human GRCh38 chr20: 56,404,812-56,404,812 , GRCh37.p13 chr20: 54,979,868-54,979,868 CSTF1
    nsv5178793mobile element insertion1nstd203human GRCh38 chr20: 56,404,809-56,404,832 , GRCh37.p13 chr20: 54,979,865-54,979,888 CSTF1
    nsv5166727mobile element insertion1nstd203human GRCh38 chr20: 56,404,811-56,404,838 , GRCh37.p13 chr20: 54,979,867-54,979,894 CSTF1
    nsv5164369mobile element insertion1nstd203human GRCh38 chr20: 56,404,812-56,404,838 , GRCh37.p13 chr20: 54,979,868-54,979,894 CSTF1
    nsv5163556mobile element insertion1nstd203human GRCh38 chr20: 56,396,402-56,396,411 , GRCh37.p13 chr20: 54,971,458-54,971,467 CSTF1
    nsv5013293copy number variation1nstd200human GRCh38 chr20: 56,400,806-56,402,667 , GRCh37.p13 chr20: 54,975,862-54,977,723 CSTF1
    nsv4853981copy number variation1nstd200human GRCh37 chr20: 54,977,346-54,977,908 , GRCh38.p12 chr20: 56,402,290-56,402,852 CSTF1
    nsv4500305mobile element insertion1nstd166human GRCh37.p13 chr20: 54,971,458-54,971,458 , GRCh38.p12 chr20: 56,396,402-56,396,402 CSTF1
    nsv4357849copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528 RBM38, LAMA5, 192 more genes
    nsv4291281copy number variation1nstd166human GRCh37.p13 chr20: 54,977,966-55,090,030 , GRCh38.p12 chr20: 56,402,910-56,514,974 , CSTF1, 4 more genes
    nsv4290085copy number variation1nstd166human GRCh37.p13 chr20: 54,964,000-54,969,000 , GRCh38.p12 chr20: 56,388,944-56,393,944 AURKA, CSTF1
    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
    nsv3918295copy number variation1nstd102humanPathogenic GRCh38 chr20: 54,594,888-58,190,583 , NCBI36 chr20: 52,644,834-56,199,045 , GRCh37 chr20: 53,211,427-56,765,639 MTRNR2L3, LOC105372687, 59 more genes
    nsv3915005copy number variation1nstd102humanPathogenic NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321 FTLP1, RNA5SP487, 472 more genes
    nsv3912982copy number variation1nstd102humanLikely pathogenic NCBI36 chr20: 53,639,062-58,949,658 , GRCh37 chr20: 54,220,678-59,516,263 , GRCh38 chr20: 55,630,597-60,941,207 ATP5F1E, BMP7, 103 more genes
    nsv3911673copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,773,088-62,908,674 , NCBI36 chr20: 54,206,495-62,379,118 , GRCh38 chr20: 56,198,032-64,277,321 LOC105372709, NPBWR2, 226 more genes
    nsv3910818copy number variation1nstd102humanUncertain significance NCBI36 chr20: 25,616,026-62,435,964 , GRCh37.p13 chr20: 25,668,026-62,965,520 , GRCh38.p12 chr20: 25,687,390-64,334,167 RNA5SP481, LOC105372625, 855 more genes
    nsv3910223copy number variation1nstd102humanLikely pathogenic NCBI36 chr20: 51,286,111-62,385,999 , GRCh37 chr20: 51,852,704-62,915,555 , GRCh38 chr20: 53,236,165-64,284,202 ATP5F1E, BMP7, 253 more genes
    nsv3905072copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435 LRRN4, SNRPB, 1313 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