U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 27

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4681277copy number variation1nstd102humanPathogenic GRCh37 chr1: 43,394,583-43,409,012 , GRCh38.p12 chr1: 42,928,912-42,943,341 SLC2A1
    nsv3886060copy number variation1nstd102humanPathogenic GRCh38 chr1: 42,927,021-42,931,226 , GRCh37 chr1: 43,392,692-43,396,897 SLC2A1
    nsv6310874copy number variation1nstd102humanPathogenic GRCh37 chr1: 43,392,712-43,396,897 , GRCh38.p12 chr1: 42,927,041-42,931,226 SLC2A1
    nsv6310809copy number variation1nstd102humanPathogenic GRCh37 chr1: 43,391,628-43,393,369 , GRCh38.p12 chr1: 42,925,957-42,927,698 SLC2A1
    nsv3885042copy number variation1nstd102humanPathogenic GRCh37 chr1: 43,395,524-43,396,897 , GRCh38 chr1: 42,929,853-42,931,226 SLC2A1
    nsv6310810copy number variation1nstd102humanPathogenic GRCh37 chr1: 43,395,244-43,395,726 , GRCh38.p12 chr1: 42,929,573-42,930,055 SLC2A1
    nsv6310508copy number variation1nstd102humanPathogenic GRCh38 chr1: 42,943,225-42,943,286 , GRCh37 chr1: 43,408,896-43,408,957 SLC2A1
    nsv3876675copy number variation1nstd102humanPathogenic GRCh38 chr1: 42,925,375-42,959,176 , GRCh37 chr1: 43,391,046-43,424,847 SLC2A1, SLC2A1-DT
    nsv5980428copy number variation1nstd102humanPathogenic GRCh37 chr1: 43,392,711-43,424,322 , GRCh38.p12 chr1: 42,927,040-42,958,651 SLC2A1, SLC2A1-DT
    nsv6310875copy number variation1nstd102humanPathogenic GRCh37 chr1: 43,424,285-43,424,429 , GRCh38.p12 chr1: 42,958,614-42,958,758 SLC2A1, SLC2A1-DT
    nsv4682186copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr1: 43,424,285-43,424,342 , GRCh38.p12 chr1: 42,958,614-42,958,671 SLC2A1, SLC2A1-DT
    nsv2779219copy number variation1nstd45humanPathogenic GRCh38.p12 chr1: 42,925,375-42,959,176 , GRCh37 chr1: 43,391,046-43,424,847 SLC2A1, SLC2A1-DT
    nsv5564407copy number variation1nstd102humanUncertain significance GRCh37 chr1: 43,392,692-43,424,342 , GRCh38.p12 chr1: 42,927,021-42,958,671 SLC2A1, SLC2A1-DT
    nsv3892747copy number variation1nstd102humanPathogenic NCBI36 chr1: 40,700,674-44,906,299 , GRCh37 chr1: 40,928,087-45,133,712 , GRCh38 chr1: 40,462,415-44,668,040 SLC2A1, ERMAP, 116 more genes
    nsv3900473copy number variation1nstd102humanPathogenic GRCh38 chr1: 40,693,289-44,514,104 , GRCh37 chr1: 41,158,961-44,979,776 , NCBI36 chr1: 40,931,548-44,752,363 SLC2A1, KDM4A, 102 more genes
    nsv3908884copy number variation1nstd102humanPathogenic GRCh37 chr1: 41,300,076-43,588,742 , GRCh38 chr1: 40,834,404-43,123,071 , NCBI36 chr1: 41,072,663-43,361,329 SLC2A1, PPCS, 46 more genes
    nsv3870704copy number variation1nstd102humanPathogenic GRCh37 chr1: 42,914,303-45,001,279 , GRCh38.p12 chr1: 42,448,632-44,535,607 SLC2A1, TMEM269-DT, 74 more genes
    nsv4451506copy number variation1nstd102humanPathogenic GRCh37 chr1: 43,336,799-44,713,202 , GRCh38.p12 chr1: 42,871,128-44,247,530 SLC2A1, CCDC24, 54 more genes
    nsv5673174copy number variation1nstd102humanPathogenic GRCh37 chr1: 43,392,692-43,870,241 , GRCh38.p12 chr1: 42,927,021-43,404,570 SLC2A1, TMEM125, 19 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 SLC2A1, MARK1, 4930 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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