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 305

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974866inversion1nstd209human GRCh38 chr1: 184,002,207-184,006,736 , GRCh37.p13 chr1: 183,971,341-183,975,870 COLGALT2
    nsv5964476insertion1nstd209human GRCh38 chr1: 184,000,537-184,000,537 , GRCh37.p13 chr1: 183,969,671-183,969,671 COLGALT2
    nsv5880578copy number variation1nstd209human GRCh38 chr1: 184,002,928-184,002,986 , GRCh37.p13 chr1: 183,972,062-183,972,120 COLGALT2
    nsv5828573copy number variation1nstd209human GRCh38 chr1: 184,002,196-184,007,631 , GRCh37.p13 chr1: 183,971,330-183,976,765 COLGALT2
    nsv5623428insertion1nstd207human GRCh38 chr1: 183,994,050-183,994,050 , GRCh37.p13 chr1: 183,963,184-183,963,184 COLGALT2
    nsv5621412insertion1nstd207human GRCh38 chr1: 184,000,537-184,000,537 , GRCh37.p13 chr1: 183,969,671-183,969,671 COLGALT2
    nsv5449356copy number variation1nstd206human GRCh38 chr1: 184,002,000-184,007,500 , GRCh37.p13 chr1: 183,971,134-183,976,634 COLGALT2
    nsv5384761copy number variation1nstd186human GRCh37 chr1: 183,963,181-183,963,690 , GRCh38.p12 chr1: 183,994,047-183,994,556 COLGALT2
    nsv5383386copy number variation1nstd186human GRCh37 chr1: 183,963,181-183,963,689 , GRCh38.p12 chr1: 183,994,047-183,994,555 COLGALT2
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5372182translocation1nstd200human GRCh38 chr1: 184,006,316-184,006,316 , GRCh38 chr1: 184,007,608-184,007,608 , GRCh37.p13 chr1: 183,975,450-183,975,450 , GRCh37.p13 chr1: 183,976,742-183,976,742 COLGALT2
    nsv5372179translocation1nstd200human GRCh38 chr1: 184,002,209-184,002,209 , GRCh38 chr1: 184,006,737-184,006,737 , GRCh37.p13 chr1: 183,971,343-183,971,343 , GRCh37.p13 chr1: 183,975,871-183,975,871 COLGALT2
    nsv5372173translocation1nstd200human GRCh38 chr1: 183,957,045-183,957,045 , GRCh38 chr1: 183,956,291-183,956,291 , GRCh37.p13 chr1: 183,925,425-183,925,425 , GRCh37.p13 chr1: 183,926,179-183,926,179 COLGALT2
    nsv5372170translocation1nstd200human GRCh38 chr1: 183,957,049-183,957,049 , GRCh38 chr1: 183,956,001-183,956,001 , GRCh37.p13 chr1: 183,926,183-183,926,183 , GRCh37.p13 chr1: 183,925,135-183,925,135 COLGALT2
    nsv5345155translocation1nstd200human GRCh37 chr1: 183,925,425-183,925,425 , GRCh37 chr1: 183,926,179-183,926,179 , GRCh38.p12 chr1: 183,957,045-183,957,045 , GRCh38.p12 chr1: 183,956,291-183,956,291 COLGALT2
    nsv5345044translocation1nstd200human GRCh37 chr1: 183,925,135-183,925,135 , GRCh37 chr1: 183,926,183-183,926,183 , GRCh38.p12 chr1: 183,956,001-183,956,001 , GRCh38.p12 chr1: 183,957,049-183,957,049 COLGALT2
    nsv5336330translocation1nstd200human GRCh37 chr1: 183,971,343-183,971,343 , GRCh37 chr1: 183,975,871-183,975,871 , GRCh38.p12 chr1: 184,002,209-184,002,209 , GRCh38.p12 chr1: 184,006,737-184,006,737 COLGALT2
    nsv5334611translocation1nstd200human GRCh37 chr1: 183,976,742-183,976,742 , GRCh37 chr1: 183,975,450-183,975,450 , GRCh38.p12 chr1: 184,007,608-184,007,608 , GRCh38.p12 chr1: 184,006,316-184,006,316 COLGALT2
    nsv5207064copy number variation1nstd204human GRCh38.p13 chr1: 183,978,601-183,980,700 , GRCh37.p13 chr1: 183,947,735-183,949,834 COLGALT2
    nsv5077313mobile element insertion1nstd203human GRCh38 chr1: 183,949,529-183,949,546 , GRCh37.p13 chr1: 183,918,663-183,918,680 COLGALT2
    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