U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Nucleotide

Items: 1 to 20 of 468

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142926insertion1nstd232human GRCh37.p13 chr19: 22,373,449-22,373,449 , GRCh38.p12 chr19: 22,190,647-22,190,647 , GRCh38.p12 chr19|NW_003315965.1: 118,227-118,227 ZNF676
    nsv7141871copy number variation1nstd232human GRCh37.p13 chr19: 22,436,188-22,436,267 , GRCh38.p12 chr19: 22,253,386-22,253,465 , GRCh38.p12 chr19|NW_003315965.1: 47,202-47,281 0
    nsv7139549copy number variation1nstd232human GRCh37.p13 chr19: 22,436,186-22,436,267 , GRCh38.p12 chr19: 22,253,384-22,253,465 , GRCh38.p12 chr19|NW_003315965.1: 47,202-47,283 0
    nsv6624849copy number variation1nstd224human GRCh37 chr19: 22,272,615-22,470,368 , GRCh38.p12 chr19: 22,089,813-22,287,566 , GRCh38.p12 chr19|NW_003315965.1: 13,101-188,024 ZNF257, ZNF676, 6 more genes
    nsv6624848copy number variation3nstd224human GRCh37 chr19: 22,226,289-22,425,615 , GRCh38.p12 chr19: 22,043,487-22,242,813 , GRCh38.p12 chr19|NW_003315965.1: 57,854-188,024 ZNF257, ZNF676, 7 more genes
    nsv6624451copy number variation1nstd224human GRCh37 chr19: 22,269,847-22,347,554 , GRCh38.p12 chr19: 22,087,045-22,164,752 , GRCh38.p12 chr19|NW_003315965.1: 144,122-188,024 MTDHP5, ZNF257, 2 more genes
    nsv6133694copy number variation1nstd213human GRCh37 chr19: 22,260,000-22,630,001 , GRCh38.p12 chr19: 22,077,198-22,447,199 , GRCh38.p12 chr19|NW_003315965.1: 1-188,024 , ZNF257, 12 more genes
    nsv6131338insertion1nstd186human GRCh37 chr19: 22,373,464-22,373,500 , GRCh38.p12 chr19|NW_003315965.1: 118,176-118,212 , GRCh38.p12 chr19: 22,190,662-22,190,698 ZNF676
    nsv5341389translocation1nstd200human GRCh37 chr19: 22,318,321-22,318,321 , GRCh37 chr19: 22,318,243-22,318,243 , GRCh38.p12 chr19|NW_003315965.1: 173,355-173,355 , GRCh38.p12 chr19|NW_003315965.1: 173,433-173,433 , GRCh38.p12 chr19: 22,135,441-22,135,441 , GRCh38.p12 chr19: 22,135,519-22,135,519 0
    nsv4860817copy number variation1nstd200human GRCh37 chr19: 22,459,323-22,462,872 , GRCh38.p12 chr19|NW_003315965.1: 20,598-24,147 , GRCh38.p12 chr19: 22,276,521-22,280,070 0
    nsv4860816copy number variation1nstd200human GRCh37 chr19: 22,451,618-22,456,311 , GRCh38.p12 chr19: 22,268,816-22,273,509 , GRCh38.p12 chr19|NW_003315965.1: 27,159-31,852 0
    nsv4860815copy number variation1nstd200human GRCh37 chr19: 22,448,273-22,450,154 , GRCh38.p12 chr19: 22,265,471-22,267,352 , GRCh38.p12 chr19|NW_003315965.1: 33,315-35,196 0
    nsv4860814copy number variation1nstd200human GRCh37 chr19: 22,422,998-22,426,521 , GRCh38.p12 chr19|NW_003315965.1: 56,948-60,471 , GRCh38.p12 chr19: 22,240,196-22,243,719
    nsv4860813copy number variation1nstd200human GRCh37 chr19: 22,312,074-22,314,130 , GRCh38.p12 chr19|NW_003315965.1: 177,546-179,602 , GRCh38.p12 chr19: 22,129,272-22,131,328 ZNF92P2
    nsv4860809copy number variation1nstd200human GRCh37 chr19: 22,206,178-22,486,074 , GRCh38.p12 chr19: 22,023,376-22,303,272 , GRCh38.p12 chr19|NW_003315965.1: 1-188,024 , PCGF7P, 11 more genes
    nsv4765891insertion1nstd199human GRCh37 chr19: 22,396,444-22,396,444 , GRCh38.p12 chr19: 22,213,642-22,213,642 , GRCh38.p12 chr19|NW_003315965.1: 95,252-95,252 0
    nsv4757347insertion1nstd199human GRCh37 chr19: 22,373,461-22,373,461 , GRCh38.p12 chr19|NW_003315965.1: 118,215-118,215 , GRCh38.p12 chr19: 22,190,659-22,190,659 ZNF676
    nsv4748475copy number variation1nstd199human GRCh37 chr19: 22,363,673-22,363,761 , GRCh38.p12 chr19: 22,180,871-22,180,959 , GRCh38.p12 chr19|NW_003315965.1: 127,915-128,003 ZNF676
    nsv4745525copy number variation1nstd199human GRCh37 chr19: 22,436,136-22,436,223 , GRCh38.p12 chr19: 22,253,334-22,253,421 , GRCh38.p12 chr19|NW_003315965.1: 47,246-47,333
    nsv4719700insertion1nstd186human GRCh37 chr19: 22,373,449-22,373,449 , GRCh38.p12 chr19|NW_003315965.1: 118,227-118,227 , GRCh38.p12 chr19: 22,190,647-22,190,647 ZNF676
    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