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 117

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7136978copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 64,081,111-64,125,347 , GRCh38.p12 chr8: 63,168,552-63,212,789 YTHDF3, YTHDF3-DT
    nsv7062610inversion1nstd229human GRCh38 chr8: 60,977,244-66,075,546 , GRCh37.p13 chr8: 61,889,803-66,987,781 LOC105375870, LINC01289, 55 more genes
    nsv6852273copy number variation1nstd229human GRCh38 chr8: 61,996,129-66,319,713 , GRCh37.p13 chr8: 62,908,688-67,231,948 LOC112268028, LOC105375873, 52 more genes
    nsv6636356copy number variation1nstd102humanUncertain significance GRCh37 chr8: 64,049,070-66,671,663 , GRCh38.p12 chr8: 63,136,511-65,759,428 LOC107986949, LOC107986878, 31 more genes
    nsv6425888copy number variation1nstd223human GRCh38 chr8: 63,163,101-63,167,200 , GRCh37.p13 chr8: 64,075,660-64,079,759 YTHDF3-DT, YTHDF3
    nsv6423791copy number variation1nstd223human GRCh38 chr8: 63,160,301-63,183,800 , GRCh37.p13 chr8: 64,072,860-64,096,359 YTHDF3, YTHDF3-DT
    nsv6136690copy number variation1nstd213human GRCh37 chr8: 64,070,000-66,540,001 , GRCh38.p12 chr8: 63,157,441-65,627,766 ARMC1, LINC01289, 27 more genes
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv4601629copy number variation1nstd183human GRCh37 chr8: 64,081,235-64,081,279 , GRCh38.p12 chr8: 63,168,676-63,168,720 YTHDF3-DT, YTHDF3
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv3924415copy number variation1nstd102humanPathogenic GRCh37 chr8: 61,431,781-67,571,260 , GRCh38 chr8: 60,519,222-66,659,025 , NCBI36 chr8: 61,594,335-67,733,814 RN7SKP135, TRIM55, 77 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3922631copy number variation1nstd102humanPathogenic GRCh38 chr8: 61,691,800-82,537,696 , NCBI36 chr8: 62,766,913-83,612,486 , GRCh37 chr8: 62,604,359-83,449,931 NCOA2, LOC107986893, 284 more genes
    nsv3919282copy number variation1nstd102humanPathogenic GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824 MIR4662B, LOC101927845, 2104 more genes
    nsv3919200copy number variation1nstd102humanPathogenic GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639 LOC112268023, LOC105375925, 2103 more genes
    nsv3918367copy number variation1nstd102humanUncertain significance GRCh37 chr8: 63,510,564-64,734,782 , NCBI36 chr8: 63,673,118-64,897,336 , GRCh38 chr8: 62,598,005-63,822,225 LOC105375876, GGH, 17 more genes
    nsv3916777copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575 RPL5P22, ARHGEF10, 2105 more genes
    nsv3916768copy number variation1nstd102humanPathogenic NCBI36 chr8: 47,062,121-70,378,576 , GRCh37 chr8: 46,942,956-70,216,022 , GRCh38 chr8: 46,031,334-69,303,787 RPL7L1P18, LINC03018, 316 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