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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147386insertion1nstd232human GRCh37.p13 chr5: 111,496,993-111,496,993 , GRCh38.p12 chr5: 112,161,296-112,161,296 EPB41L4A, EPB41L4A-AS1, 1 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
    nsv6778012copy number variation1nstd229human GRCh38 chr5: 112,105,834-112,195,471 , GRCh37.p13 chr5: 111,441,531-111,531,168 EPB41L4A, EPB41L4A-AS1, 1 more genes
    nsv6776921copy number variation1nstd229human GRCh38 chr5: 112,156,265-112,162,462 , GRCh37.p13 chr5: 111,491,962-111,498,159 SNORA13, EPB41L4A, 1 more genes
    nsv6772948copy number variation1nstd229human GRCh38 chr5: 112,127,101-112,161,000 , GRCh37.p13 chr5: 111,462,798-111,496,697 EPB41L4A, EPB41L4A-AS1, 1 more genes
    nsv6763798copy number variation1nstd229human GRCh38 chr5: 111,959,103-112,732,497 , GRCh37.p13 chr5: 111,294,800-112,068,194 EPB41L4A-DT, LINC02200, 10 more genes
    nsv6762826copy number variation1nstd229human GRCh38 chr5: 112,061,006-112,699,809 , GRCh37.p13 chr5: 111,396,703-112,035,506 TMEM183AP6, LOC102467216, 7 more genes
    nsv6758111copy number variation1nstd229human GRCh38 chr5: 112,126,562-112,160,727 , GRCh37.p13 chr5: 111,462,259-111,496,424 SNORA13, EPB41L4A-AS1, 1 more genes
    nsv6636484copy number variation1nstd102humanUncertain significance GRCh37 chr5: 111,424,127-111,508,288 , GRCh38.p12 chr5: 112,088,430-112,172,591 EPB41L4A, EPB41L4A-AS1, 1 more genes
    nsv6400014copy number variation1nstd223human GRCh38 chr5: 112,085,398-112,780,300 , GRCh37.p13 chr5: 111,421,095-112,115,997 EPB41L4A-AS1, TMEM183AP6, 10 more genes
    nsv6313698copy number variation1nstd102humanPathogenic GRCh37 chr5: 111,443,783-116,255,660 , GRCh38.p12 chr5: 112,108,086-116,919,964 RPS17P2, COMMD10, 71 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
    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
    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
    nsv6134968copy number variation1nstd213human GRCh37 chr5: 111,270,000-111,580,001 , GRCh38.p12 chr5: 111,934,303-112,244,304 NREP, EPB41L4A, 4 more genes
    nsv5557808sequence alteration1nstd206human GRCh38 chr5: 112,113,105-112,239,224 , GRCh37.p13 chr5: 111,448,802-111,574,921 EPB41L4A, EPB41L4A-AS1, 2 more genes
    nsv5466197copy number variation1nstd206human GRCh38 chr5: 112,130,729-112,188,052 , GRCh37.p13 chr5: 111,466,426-111,523,749 EPB41L4A, EPB41L4A-AS1, 1 more genes
    nsv5465317copy number variation1nstd206human GRCh38 chr5: 112,057,402-112,192,469 , GRCh37.p13 chr5: 111,393,099-111,528,166 EPB41L4A, EPB41L4A-AS1, 1 more genes
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
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