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 162

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6762157copy number variation1nstd229human GRCh38 chr5: 111,368,096-111,533,019 , GRCh37.p13 chr5: 110,703,794-110,868,717 STARD4, STARD4-AS1, 2 more genes
    nsv6761248copy number variation1nstd229human GRCh38 chr5: 111,385,856-111,589,981 , GRCh37.p13 chr5: 110,721,554-110,925,678 STARD4, HMGN1P13, 3 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
    nsv6404118copy number variation1nstd223human GRCh38 chr5: 111,509,964-111,523,519 , GRCh37.p13 chr5: 110,845,662-110,859,217 STARD4, LOC105369177, 1 more genes
    nsv6399407copy number variation1nstd223human GRCh38 chr5: 111,496,801-111,498,200 , GRCh37.p13 chr5: 110,832,499-110,833,898 STARD4, CAMK4
    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
    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
    nsv6064137insertion1nstd212human GRCh38 chr5: 111,495,522-111,495,522 , GRCh37.p13 chr5: 110,831,220-110,831,220 CAMK4, STARD4
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
    nsv4679460copy number variation1nstd189human GRCh37.p13 chr5: 110,742,798-111,062,961 , GRCh38.p12 chr5: 111,407,100-111,727,264 CAMK4, NREP, 5 more genes
    nsv4589732copy number variation1nstd183human GRCh37 chr5: 110,847,875-110,850,480 , GRCh38.p12 chr5: 111,512,177-111,514,782 LOC105369177, STARD4, 1 more genes
    nsv4484742mobile element insertion1nstd166human GRCh37.p13 chr5: 110,831,635-110,831,635 , GRCh38.p12 chr5: 111,495,937-111,495,937 STARD4, CAMK4
    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