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 311

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143060insertion1nstd232human GRCh37.p13 chr6: 35,837,677-35,837,677 , GRCh38.p12 chr6: 35,869,900-35,869,900 SRPK1
    nsv7143029insertion1nstd232human GRCh37.p13 chr6: 35,858,790-35,858,790 , GRCh38.p12 chr6: 35,891,013-35,891,013 SRPK1
    nsv7098787copy number variation1nstd102humanUncertain significance GRCh37 chr6: 32,148,920-36,953,949 , GRCh38.p12 chr6: 32,181,143-36,986,173 CUTA, SYNGAP1, 184 more genes
    nsv7097426copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-36,953,949 , GRCh38.p12 chr6: 30,728,116-36,986,173 LEMD2, PSORS1C1, 321 more genes
    nsv7053830inversion1nstd229human GRCh38 chr6: 29,164,448-38,692,657 , GRCh37.p13 chr6: 29,132,225-38,660,433 GTF2H4, RNF8, 472 more genes
    nsv7046831inversion1nstd229human GRCh38 chr6: 35,228,579-36,340,036 , GRCh37.p13 chr6: 35,196,356-36,307,813 MAPK14, TEAD3, 34 more genes
    nsv7046729inversion1nstd229human GRCh38 chr6: 35,747,390-37,934,033 , GRCh37.p13 chr6: 35,715,167-37,901,809 MAPK14, LAP3P2, 58 more genes
    nsv7045112inversion1nstd229human GRCh38 chr6: 30,561,326-37,907,708 , GRCh37.p13 chr6: 30,529,103-37,875,484 ZBTB22, PNPLA1, 355 more genes
    nsv6797193copy number variation1nstd229human GRCh38 chr6: 35,839,683-35,842,166 , GRCh37.p13 chr6: 35,807,460-35,809,943 SRPK1
    nsv6796160copy number variation1nstd229human GRCh38 chr6: 35,916,009-35,916,044 , GRCh37.p13 chr6: 35,883,786-35,883,821 SRPK1
    nsv6795505copy number variation1nstd229human GRCh38 chr6: 35,843,934-35,852,429 , GRCh37.p13 chr6: 35,811,711-35,820,206 SRPK1
    nsv6793447copy number variation1nstd229human GRCh38 chr6: 35,912,823-35,917,371 , GRCh37.p13 chr6: 35,880,600-35,885,148 SRPK1
    nsv6792078copy number variation1nstd229human GRCh38 chr6: 35,850,004-35,852,182 , GRCh37.p13 chr6: 35,817,781-35,819,959 SRPK1
    nsv6789750copy number variation1nstd229human GRCh38 chr6: 35,890,819-35,890,854 , GRCh37.p13 chr6: 35,858,596-35,858,631 SRPK1
    nsv6789650copy number variation1nstd229human GRCh38 chr6: 35,664,001-35,837,700 , GRCh37.p13 chr6: 35,631,778-35,805,477 CLPSL2, CMPK1P1, 8 more genes
    nsv6783433copy number variation1nstd229human GRCh38 chr6: 35,686,686-35,881,967 , GRCh37.p13 chr6: 35,654,463-35,849,744 ARMC12, CLPSL1, 7 more genes
    nsv6780005copy number variation1nstd229human GRCh38 chr6: 35,898,347-35,900,386 , GRCh37.p13 chr6: 35,866,124-35,868,163 SRPK1
    nsv6574904inversion1nstd223human GRCh38 chr6: 35,914,964-35,915,213 , GRCh37.p13 chr6: 35,882,741-35,882,990 SRPK1
    nsv6570358inversion1nstd223human GRCh38 chr6: 32,570,902-37,403,160 , GRCh37.p13 chr6: 32,538,679-37,370,936 RN7SL273P, MKRN6P, 177 more genes
    nsv6566225inversion1nstd223human GRCh38 chr6: 35,867,647-35,868,162 , GRCh37.p13 chr6: 35,835,424-35,835,939 SRPK1
    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