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 179

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv7146934copy number variation1nstd232human GRCh37.p13 chr8: 48,875,417-48,875,501 , GRCh38.p12 chr8: 47,962,857-47,962,941 MCM4
    nsv7144912insertion1nstd232human GRCh37.p13 chr8: 48,883,437-48,883,437 , GRCh38.p12 chr8: 47,970,877-47,970,877 MCM4
    nsv7141470copy number variation1nstd232human GRCh37.p13 chr8: 48,874,775-48,874,862 , GRCh38.p12 chr8: 47,962,215-47,962,302 MCM4
    nsv7139982insertion1nstd232human GRCh37.p13 chr8: 48,874,239-48,874,239 , GRCh38.p12 chr8: 47,961,679-47,961,679 MCM4
    nsv7098177copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,873,705-48,875,620 , GRCh38.p12 chr8: 47,961,145-47,963,060 MCM4
    nsv7097663copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,686,734-48,872,686 , GRCh38.p12 chr8: 47,774,173-47,960,126 PRKDC, LOC105375818, 1 more genes
    nsv6850722copy number variation1nstd229human GRCh38 chr8: 47,597,201-48,026,222 , GRCh37.p13 chr8: 48,509,763-48,938,782 CEBPD, RNU6-519P, 7 more genes
    nsv6850167copy number variation1nstd229human GRCh38 chr8: 47,965,720-47,972,753 , GRCh37.p13 chr8: 48,878,280-48,885,313 MCM4
    nsv6845265copy number variation1nstd229human GRCh38 chr8: 47,745,303-48,130,564 , GRCh37.p13 chr8: 48,657,865-49,043,124 UBE2V2-AS1, MCM4, 5 more genes
    nsv6839795copy number variation1nstd229human GRCh38 chr8: 47,978,627-47,979,007 , GRCh37.p13 chr8: 48,891,187-48,891,567 MCM4, RNU6-519P
    nsv6838616copy number variation1nstd229human GRCh38 chr8: 47,969,023-47,969,101 , GRCh37.p13 chr8: 48,881,583-48,881,661 MCM4
    nsv6633064copy number variation1nstd224human GRCh37 chr8: 48,691,637-49,066,992 , GRCh38.p12 chr8: 47,779,076-48,154,432 MCM4, PRKDC, 5 more genes
    nsv6569657inversion1nstd223human GRCh38 chr8: 47,319,822-52,044,550 , GRCh37.p13 chr8: 48,405,007-52,957,110 UBE2V2-AS1, BRIX1P1, 48 more genes
    nsv6567065inversion1nstd223human GRCh38 chr8: 47,971,987-47,972,828 , GRCh37.p13 chr8: 48,884,547-48,885,388 MCM4
    nsv6566764inversion1nstd223human GRCh38 chr8: 47,958,872-47,959,686 , GRCh37.p13 chr8: 48,871,432-48,872,246 PRKDC, MCM4
    nsv6431005copy number variation1nstd223human GRCh38 chr8: 47,967,059-48,023,595 , GRCh37.p13 chr8: 48,879,619-48,936,155 RNU6-519P, UBE2V2, 2 more genes
    nsv6424060copy number variation1nstd223human GRCh38 chr8: 47,957,804-47,959,008 , GRCh37.p13 chr8: 48,870,364-48,871,568 PRKDC, MCM4
    nsv6421696copy number variation1nstd223human GRCh38 chr8: 47,978,496-47,983,681 , GRCh37.p13 chr8: 48,891,056-48,896,241 RNU6-519P, MCM4
    nsv6419939copy number variation1nstd223human GRCh38 chr8: 47,978,362-47,979,706 , GRCh37.p13 chr8: 48,890,922-48,892,266 RNU6-519P, MCM4
    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