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 192

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129539insertion1nstd186human GRCh37 chr17: 76,139,179-76,139,179 , GRCh38.p12 chr17: 78,143,098-78,143,098 TMC8
    nsv5660757insertion1nstd207human GRCh38 chr17: 78,143,074-78,143,074 , GRCh37.p13 chr17: 76,139,155-76,139,155 TMC8
    nsv5536343insertion1nstd206human GRCh38 chr17: 78,143,098-78,143,098 , GRCh37.p13 chr17: 76,139,179-76,139,179 TMC8
    nsv5296713copy number variation1nstd204human GRCh38.p13 chr17: 78,128,828-78,131,322 , GRCh37.p13 chr17: 76,124,909-76,127,403 TMC8, TMC6
    nsv5158575mobile element insertion1nstd203human GRCh38 chr17: 78,143,122-78,143,169 , GRCh37.p13 chr17: 76,139,203-76,139,250 TMC8
    nsv5158504mobile element insertion1nstd203human GRCh38 chr17: 78,143,017-78,143,063 , GRCh37.p13 chr17: 76,139,098-76,139,144 TMC8
    nsv5158256mobile element insertion1nstd203human GRCh38 chr17: 78,143,097-78,143,122 , GRCh37.p13 chr17: 76,139,178-76,139,203 TMC8
    nsv5152982mobile element insertion1nstd203human GRCh38 chr17: 78,142,991-78,143,017 , GRCh37.p13 chr17: 76,139,072-76,139,098 TMC8
    nsv5150972mobile element insertion1nstd203human GRCh38 chr17: 78,142,971-78,143,017 , GRCh37.p13 chr17: 76,139,052-76,139,098 TMC8
    nsv5147823mobile element insertion1nstd203human GRCh38 chr17: 78,142,989-78,143,017 , GRCh37.p13 chr17: 76,139,070-76,139,098 TMC8
    nsv5147176mobile element insertion1nstd203human GRCh38 chr17: 78,143,076-78,143,122 , GRCh37.p13 chr17: 76,139,157-76,139,203 TMC8
    nsv5146692mobile element insertion1nstd203human GRCh38 chr17: 78,142,998-78,143,017 , GRCh37.p13 chr17: 76,139,079-76,139,098 TMC8
    nsv5145238mobile element insertion1nstd203human GRCh38 chr17: 78,143,075-78,143,122 , GRCh37.p13 chr17: 76,139,156-76,139,203 TMC8
    nsv5144152mobile element insertion1nstd203human GRCh38 chr17: 78,142,988-78,143,017 , GRCh37.p13 chr17: 76,139,069-76,139,098 TMC8
    nsv5143970mobile element insertion1nstd203human GRCh38 chr17: 78,142,994-78,143,017 , GRCh37.p13 chr17: 76,139,075-76,139,098 TMC8
    nsv5035778inversion1nstd200human GRCh38 chr17: 78,138,562-78,604,810 , GRCh37.p13 chr17: 76,134,643-76,600,892 , DNAH17-AS1, 20 more genes
    nsv4758960insertion1nstd199human GRCh37 chr17: 76,139,138-76,139,138 , GRCh38.p12 chr17: 78,143,057-78,143,057 TMC8
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4633960copy number variation1nstd183human GRCh37 chr17: 76,122,654-76,127,621 , GRCh38.p12 chr17: 78,126,573-78,131,540 TMC8, TMC6
    nsv4532092copy number variation1nstd166human GRCh37.p13 chr17: 76,130,521-76,130,879 , GRCh38.p12 chr17: 78,134,440-78,134,798 TMC8
    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