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
    nsv7096308copy number variation1nstd102humanUncertain significance GRCh37 chr22: 35,776,672-42,486,826 , GRCh38.p12 chr22: 35,380,679-42,090,822 CDC42EP1, SREBF2, 231 more genes
    nsv7077764inversion1nstd229human GRCh38 chr22: 37,971,370-41,589,449 , GRCh37.p13 chr22: 38,367,377-41,985,453 UQCRFS1P1, LOC105373027, 119 more genes
    nsv7070838inversion1nstd229human GRCh38 chr22: 40,481,826-41,015,795 , GRCh37.p13 chr22: 40,877,830-41,411,799 RFKP4, COX6B1P3, 14 more genes
    nsv7064338inversion1nstd229human GRCh38 chr22: 40,322,864-40,533,291 , GRCh37.p13 chr22: 40,718,868-40,929,295 ADSL, SGSM3, 4 more genes
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7058666inversion1nstd229human GRCh38 chr22: 39,066,437-42,707,681 , GRCh37.p13 chr22: 39,462,442-43,103,687 LOC101927344, ATF4, 128 more genes
    nsv7033741copy number variation1nstd229human GRCh38 chr22: 40,495,541-40,543,497 , GRCh37.p13 chr22: 40,891,545-40,939,501 MRTFA-AS1, MRTFA
    nsv7027741copy number variation1nstd229human GRCh38 chr22: 39,432,386-49,047,389 , GRCh37.p13 chr22: 39,828,391-49,443,201 LOC105373064, ACO2, 233 more genes
    nsv7024599copy number variation1nstd229human GRCh38 chr22: 40,520,601-40,523,500 , GRCh37.p13 chr22: 40,916,605-40,919,504 MRTFA, MRTFA-AS1
    nsv6638050copy number variation1nstd102humanPathogenic GRCh37 chr22: 40,131,240-41,556,564 , GRCh38.p12 chr22: 39,735,235-41,160,560 GRAP2, UQCRFS1P1, 32 more genes
    nsv6637214copy number variation1nstd102humanUncertain significance GRCh37 chr22: 39,768,795-41,946,225 , GRCh38.p12 chr22: 39,372,790-41,550,221 MRTFA-AS1, LOC105373043, 62 more genes
    nsv6596534inversion1nstd223human GRCh38 chr22: 39,133,553-42,757,193 , GRCh37.p13 chr22: 39,529,558-43,153,199 POLR3H, ACO2, 123 more genes
    nsv6311136copy number variation1nstd102humanUncertain significance GRCh37 chr22: 39,621,728-41,077,932 , GRCh38.p12 chr22: 39,225,723-40,681,928 TAB1, TNRC6B, 34 more genes
    nsv6217060copy number variation1nstd214human GRCh38 chr22: 40,520,987-40,521,049 , GRCh37.p13 chr22: 40,916,991-40,917,053 MRTFA, MRTFA-AS1
    nsv6134214copy number variation1nstd213human GRCh37 chr22: 40,070,000-44,960,001 , GRCh38.p12 chr22: 39,673,995-44,564,121 , ACO2, 148 more genes
    nsv6134067copy number variation1nstd213human GRCh37 chr22: 40,070,000-43,110,001 , GRCh38.p12 chr22: 39,673,995-42,713,995 ACO2, ADSL, 106 more genes
    nsv5957129copy number variation1nstd209human GRCh38 chr22: 40,520,987-40,521,049 , GRCh37.p13 chr22: 40,916,991-40,917,053 MRTFA-AS1, MRTFA
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4680014copy number variation1nstd189human GRCh37.p13 chr22: 40,744,858-41,816,746 , GRCh38.p12 chr22: 40,348,854-41,420,742 , ADSL, 37 more genes
    nsv4676292copy number variation1nstd102humanPathogenic GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410 PDXP-DT, PDGFB, 550 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