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 419

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148221copy number variation1nstd102humanPathogenic GRCh38 chr6: 150,905,553-158,511,926 , GRCh37.p13 chr6: 151,226,689-158,932,958 RNU6-824P, LOC105378067, 97 more genes
    nsv7146285copy number variation1nstd232human GRCh37.p13 chr6: 157,732,394-157,732,562 , GRCh38.p12 chr6: 157,311,362-157,311,530 TMEM242
    nsv7140750insertion1nstd232human GRCh37.p13 chr6: 157,708,675-157,708,675 , GRCh38.p12 chr6: 157,287,643-157,287,643 TMEM242
    nsv7057653inversion1nstd229human GRCh38 chr6: 155,088,001-159,627,095 , GRCh37.p13 chr6: 155,409,135-160,048,127 SNORD28B, NMTRV-TAC1-1, 62 more genes
    nsv7053022inversion1nstd229human GRCh38 chr6: 153,431,159-160,785,697 , GRCh37.p13 chr6: 153,752,294-161,206,729 OPRM1, FNDC1-AS1, 106 more genes
    nsv7052273inversion1nstd229human GRCh38 chr6: 153,428,141-160,785,922 , GRCh37.p13 chr6: 153,749,276-161,206,954 LOC442272, CACYBPP3, 106 more genes
    nsv7050008inversion1nstd229human GRCh38 chr6: 153,421,054-160,785,901 , GRCh37.p13 chr6: 153,742,189-161,206,933 SLC22A2, IGF2R, 108 more genes
    nsv7043790inversion1nstd229human GRCh38 chr6: 157,299,178-157,300,004 , GRCh37.p13 chr6: 157,720,210-157,721,036 , GRCh37.p13 chr6|NW_004775429.1: 80,614-81,440 LDHAL6FP, TMEM242
    nsv7040600inversion1nstd229human GRCh38 chr6: 153,683,778-158,739,378 , GRCh37.p13 chr6: 154,004,913-159,160,410 TMEM242, RPL17P24, 59 more genes
    nsv6811548copy number variation1nstd229human GRCh38 chr6: 157,289,401-157,297,700 , GRCh37.p13 chr6: 157,710,433-157,718,732 , GRCh37.p13 chr6|NW_004775429.1: 70,837-79,136 LDHAL6FP, TMEM242
    nsv6798862copy number variation1nstd229human GRCh38 chr6: 157,302,156-157,304,865 , GRCh37.p13 chr6|NW_004775429.1: 83,592-86,301 , GRCh37.p13 chr6: 157,723,188-157,725,897 TMEM242
    nsv6634356copy number variation1nstd102humanPathogenic GRCh37 chr6: 157,318,401-165,233,548 , GRCh38.p12 chr6: 156,997,267-164,820,059 LOC105378097, LOC105378094, 103 more genes
    nsv6600185copy number variation1nstd223human GRCh38 chr6: 157,320,382-157,321,113 , GRCh37.p13 chr6|NW_004775429.1: 101,818-102,549 , GRCh37.p13 chr6: 157,741,414-157,742,145 TMEM242
    nsv6573838inversion1nstd223human GRCh38 chr6: 153,683,778-158,757,107 , GRCh37.p13 chr6: 154,004,913-159,178,139 ARID1B, TFB1M, 59 more genes
    nsv6573818inversion1nstd223human GRCh38 chr6: 153,431,058-160,785,713 , GRCh37.p13 chr6: 153,752,193-161,206,745 MTRES1P1, SOD2-OT1, 106 more genes
    nsv6564527inversion1nstd223human GRCh38 chr6: 150,782,887-160,100,808 , GRCh37.p13 chr6: 151,104,023-160,521,840 RPL31P29, RPL17P24, 139 more genes
    nsv6562231inversion1nstd223human GRCh38 chr6: 150,783,018-160,100,808 , GRCh37.p13 chr6: 151,104,154-160,521,840 ARMT1, LOC102723831, 139 more genes
    nsv6558878inversion1nstd223human GRCh38 chr6: 153,428,103-160,785,918 , GRCh37.p13 chr6: 153,749,238-161,206,950 IGF2R, SOD2-OT1, 106 more genes
    nsv6313530copy number variation1nstd102humanPathogenic GRCh37 chr6: 153,207,930-164,322,346 , GRCh38.p12 chr6: 152,886,795-163,901,314 RSPH3, FBXO5, 144 more genes
    nsv6313489copy number variation1nstd102humanUncertain significance GRCh37 chr6: 157,261,376-157,964,661 , GRCh38.p12 chr6: 156,940,242-157,543,629 LOC100420839, MIR3692, 7 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