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 183

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098875copy number variation1nstd102humanUncertain significance GRCh37 chr5: 108,594,343-110,644,342 , GRCh38.p12 chr5: 109,258,642-111,308,644 WDR36, CT45B1P, 19 more genes
    nsv7055886inversion1nstd229human GRCh38 chr5: 110,900,937-112,489,509 , GRCh37.p13 chr5: 110,236,636-111,825,206 HMGB3P16, SNORA13, 21 more genes
    nsv7051654inversion1nstd229human GRCh38 chr5: 109,433,715-112,221,146 , GRCh37.p13 chr5: 108,769,416-111,556,843 CAMK4, PGAM5P1, 29 more genes
    nsv7040290inversion1nstd229human GRCh38 chr5: 110,957,401-111,069,855 , GRCh37.p13 chr5: 110,293,100-110,405,553 TSLP, LOC105379121, 1 more genes
    nsv6777630copy number variation1nstd229human GRCh38 chr5: 110,899,413-111,431,483 , GRCh37.p13 chr5: 110,235,112-110,767,181 CAMK4, TSLP, 6 more genes
    nsv6771316copy number variation1nstd229human GRCh38 chr5: 111,073,914-111,074,079 , GRCh37.p13 chr5: 110,409,612-110,409,777 TSLP
    nsv6770460copy number variation1nstd229human GRCh38 chr5: 110,997,111-111,331,415 , GRCh37.p13 chr5: 110,332,810-110,667,113 TSLP, CAMK4, 4 more genes
    nsv6770335copy number variation1nstd229human GRCh38 chr5: 110,985,795-111,159,296 , GRCh37.p13 chr5: 110,321,494-110,494,994 LOC100129099, WDR36, 2 more genes
    nsv6768218copy number variation1nstd229human GRCh38 chr5: 110,998,101-111,077,900 , GRCh37.p13 chr5: 110,333,800-110,413,598 LOC105379121, TSLP
    nsv6765732copy number variation1nstd229human GRCh38 chr5: 111,050,385-111,090,549 , GRCh37.p13 chr5: 110,386,083-110,426,247 WDR36, TSLP
    nsv6760573copy number variation1nstd229human GRCh38 chr5: 111,076,901-111,080,000 , GRCh37.p13 chr5: 110,412,599-110,415,698 TSLP
    nsv6636299copy number variation1nstd102humanUncertain significance GRCh37 chr5: 109,786,744-110,813,071 , GRCh38.p12 chr5: 110,451,043-111,477,373 CAMK4, RPS3AP21, 9 more genes
    nsv6630213copy number variation1nstd224human GRCh37 chr5: 110,310,810-110,411,702 , GRCh38.p12 chr5: 110,975,111-111,076,004 LOC105379121, LOC100131280, 1 more genes
    nsv6406291copy number variation1nstd223human GRCh38 chr5: 104,450,630-111,579,763 , GRCh37.p13 chr5: 103,786,331-110,915,460 STARD4, LOC285638, 46 more genes
    nsv6313580copy number variation1nstd102humanPathogenic GRCh37 chr5: 93,650,000-114,969,108 , GRCh38.p12 chr5: 94,314,295-115,633,411 FER, HMGN1P15, 222 more genes
    nsv6291318copy number variation1nstd102humanLikely benign GRCh37 chr5: 110,299,633-110,427,052 , GRCh38.p12 chr5: 110,963,934-111,091,354 WDR36, LOC100131280, 2 more genes
    nsv6135689copy number variation1nstd213human GRCh37 chr5: 96,670,000-113,570,001 , GRCh38.p12 chr5: 97,334,296-114,234,304 APC, CAMK4, 154 more genes
    nsv6135637copy number variation1nstd213human GRCh37 chr5: 110,150,000-111,090,001 , GRCh38.p12 chr5: 110,814,301-111,754,304 CAMK4, NREP, 12 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv5464023copy number variation1nstd206human GRCh38 chr5: 110,989,807-111,303,807 , GRCh37.p13 chr5: 110,325,506-110,639,505 CAMK4, TSLP, 4 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