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 416

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977326inversion1nstd209human GRCh38 chr5: 176,286,704-177,635,736 , GRCh37.p13 chr5: 175,713,707-177,062,737 , CLTB, 46 more genes
    nsv5903692copy number variation1nstd209human GRCh38 chr5: 176,304,861-176,304,937 , GRCh37.p13 chr5: 175,731,864-175,731,940 SIMC1
    nsv5901718copy number variation1nstd209human GRCh38 chr5: 172,153,284-177,326,767 , GRCh37.p13 chr5: 171,580,288-176,753,768 , LOC107986487, 114 more genes
    nsv5896983copy number variation1nstd209human GRCh38 chr5: 176,295,549-176,295,747 , GRCh37.p13 chr5: 175,722,552-175,722,750 SIMC1
    nsv5890062copy number variation1nstd209human GRCh38 chr5: 176,061,658-178,007,127 , GRCh37.p13 chr5: 175,488,661-177,434,128 , DBN1, 65 more genes
    nsv5842474copy number variation2nstd209human GRCh38 chr5: 176,246,386-176,249,741 , GRCh37.p13 chr5: 175,673,389-175,676,744 SIMC1
    nsv5842209copy number variation1nstd209human GRCh38 chr5: 176,275,750-176,277,696 , GRCh37.p13 chr5: 175,702,753-175,704,699 SIMC1
    nsv5841905copy number variation1nstd209human GRCh38 chr5: 176,255,659-176,266,304 , GRCh37.p13 chr5: 175,682,662-175,693,307 SIMC1
    nsv5841904copy number variation2nstd209human GRCh38 chr5: 176,228,745-176,237,446 , GRCh37.p13 chr5: 175,655,748-175,664,449 SIMC1, LOC107986487
    nsv5841607copy number variation2nstd209human GRCh38 chr5: 176,241,567-176,243,552 , GRCh37.p13 chr5: 175,668,570-175,670,555 SIMC1
    nsv5676056mobile element insertion1nstd211human GRCh38 chr5: 176,283,395-176,283,395 , GRCh37.p13 chr5: 175,710,398-175,710,398 SIMC1
    nsv5642683insertion1nstd207human GRCh38 chr5: 176,305,699-176,305,699 , GRCh37.p13 chr5: 175,732,702-175,732,702 SIMC1
    nsv5639862insertion1nstd207human GRCh38 chr5: 176,305,290-176,305,290 , GRCh37.p13 chr5: 175,732,293-175,732,293 SIMC1
    nsv5636663insertion1nstd207human GRCh38 chr5: 176,305,314-176,305,314 , GRCh37.p13 chr5: 175,732,317-175,732,317 SIMC1
    nsv5633965insertion1nstd207human GRCh38 chr5: 176,306,393-176,306,393 , GRCh37.p13 chr5: 175,733,396-175,733,396 SIMC1, BRCC3P1
    nsv5632877insertion1nstd207human GRCh38 chr5: 176,306,178-176,306,178 , GRCh37.p13 chr5: 175,733,181-175,733,181 BRCC3P1, SIMC1
    nsv5632528insertion1nstd207human GRCh38 chr5: 176,305,590-176,305,590 , GRCh37.p13 chr5: 175,732,593-175,732,593 SIMC1
    nsv5628461insertion1nstd207human GRCh38 chr5: 176,305,793-176,305,793 , GRCh37.p13 chr5: 175,732,796-175,732,796 SIMC1
    nsv5625868insertion1nstd207human GRCh38 chr5: 176,306,299-176,306,299 , GRCh37.p13 chr5: 175,733,302-175,733,302 SIMC1, BRCC3P1
    nsv5581183copy number variation1nstd207human GRCh38 chr5: 176,253,074-176,253,161 , GRCh37.p13 chr5: 175,680,077-175,680,164 SIMC1
    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