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 308

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148156copy number variation1nstd102humanPathogenic GRCh38 chr6: 161,349,282-170,584,790 , GRCh37.p13 chr6: 161,770,314-170,893,878 LOC105378126, LOC107986550, 149 more genes
    nsv7137133copy number variation1nstd102humanUncertain significance GRCh37 chr6: 159,006,336-170,713,678 , GRCh38.p12 chr6: 158,585,304-170,404,590 LOC101929460, GPR31, 199 more genes
    nsv7098721copy number variation1nstd102humanUncertain significance GRCh37 chr6: 170,151,754-170,599,227 , GRCh38.p12 chr6: 169,751,658-170,290,139 LOC100131532, LOC107986674, 16 more genes
    nsv7051730inversion1nstd229human GRCh38 chr6: 167,665,486-170,032,054 , GRCh37.p13 chr6: 168,066,166-170,347,278 WDR27, KIF25, 49 more genes
    nsv6807446copy number variation1nstd229human GRCh38 chr6: 169,765,858-169,766,002 , GRCh37.p13 chr6: 170,165,954-170,166,098 ERMARD
    nsv6803521copy number variation1nstd229human GRCh38 chr6: 169,766,975-169,776,760 , GRCh37.p13 chr6: 170,167,071-170,176,856 ERMARD
    nsv6802761copy number variation1nstd229human GRCh38 chr6: 169,751,301-169,831,700 , GRCh37.p13 chr6: 170,151,397-170,231,796 LINC00574, LINC00242, 2 more genes
    nsv6802005copy number variation1nstd229human GRCh38 chr6: 169,755,249-169,757,368 , GRCh37.p13 chr6: 170,155,345-170,157,464 ERMARD
    nsv6801781copy number variation1nstd229human GRCh38 chr6: 169,528,226-169,975,529 , GRCh37.p13 chr6: 169,928,322-170,279,972 LINC00242, LINC00574, 9 more genes
    nsv6800089copy number variation1nstd229human GRCh38 chr6: 169,770,979-169,779,287 , GRCh37.p13 chr6: 170,171,075-170,179,383 ERMARD
    nsv6636689copy number variation1nstd102humanPathogenic GRCh37 chr6: 163,181,847-170,919,482 , GRCh38.p12 chr6: 162,760,815-170,610,394 GNG5P1, LINC01558, 144 more genes
    nsv6634382copy number variation1nstd102humanPathogenic GRCh37 chr6: 168,552,894-170,919,482 , GRCh38.p12 chr6: 168,152,214-170,610,394 LOC101929460, LINC01624, 49 more genes
    nsv6634373copy number variation1nstd102humanPathogenic GRCh37 chr6: 163,836,226-170,893,669 , GRCh38.p12 chr6: 163,415,194-170,584,581 LOC107986547, LOC107986550, 132 more genes
    nsv6615772copy number variation1nstd223human GRCh38 chr6: 169,546,601-170,309,800 , GRCh37.p13 chr6: 169,946,697-170,618,888 ERMARD, C6orf120, 19 more genes
    nsv6614883copy number variation1nstd223human GRCh38 chr6: 169,749,201-169,754,100 , GRCh37.p13 chr6: 170,149,297-170,154,196 DYNLT2, ERMARD
    nsv6608026copy number variation1nstd223human GRCh38 chr6: 169,180,752-170,050,020 , GRCh37.p13 chr6: 169,580,847-170,365,244 DYNLT2, LOC107986675, 16 more genes
    nsv6604292copy number variation1nstd223human GRCh38 chr6: 169,644,101-169,762,500 , GRCh37.p13 chr6: 170,044,197-170,162,596 WDR27, C6orf120, 3 more genes
    nsv6603825copy number variation1nstd223human GRCh38 chr6: 169,744,701-169,757,900 , GRCh37.p13 chr6: 170,144,797-170,157,996 ERMARD, DYNLT2
    nsv6315428copy number variation1nstd102humanPathogenic GRCh37 chr6: 159,121,459-170,919,482 , GRCh38.p12 chr6: 158,700,427-170,610,394 TBP, LOC105378130, 200 more genes
    nsv6315422copy number variation1nstd102humanPathogenic GRCh37 chr6: 168,643,852-170,919,482 , GRCh38.p12 chr6: 168,243,172-170,610,394 LOC105378157, LOC105378140, 48 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