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Items: 1 to 20 of 210

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096969copy number variation1nstd102humanUncertain significance GRCh37 chr4: 148,550,590-148,578,202 , GRCh38.p12 chr4: 147,629,439-147,657,051 PRMT9, TMEM184C
    nsv7053923inversion1nstd229human GRCh38 chr4: 143,521,980-150,843,613 , GRCh37.p13 chr4: 144,443,133-151,764,765 AKIRIN2P1, PRMT9, 87 more genes
    nsv7053497inversion1nstd229human GRCh38 chr4: 147,629,146-147,631,211 , GRCh37.p13 chr4: 148,550,297-148,552,362 TMEM184C
    nsv7050914inversion1nstd229human GRCh38 chr4: 143,519,295-150,840,265 , GRCh37.p13 chr4: 144,440,448-151,761,417 MIR548G, LOC100420464, 87 more genes
    nsv6753784copy number variation1nstd229human GRCh38 chr4: 147,624,326-147,624,419 , GRCh37.p13 chr4: 148,545,477-148,545,570 TMEM184C
    nsv6749382copy number variation1nstd229human GRCh38 chr4: 147,538,037-147,970,462 , GRCh37.p13 chr4: 148,459,189-148,891,613 EDNRA, LINC02507, 7 more genes
    nsv6748200copy number variation1nstd229human GRCh38 chr4: 147,567,404-147,791,230 , GRCh37.p13 chr4: 148,488,556-148,712,381 MIR4799, LINC02507, 4 more genes
    nsv6738454copy number variation1nstd229human GRCh38 chr4: 147,627,505-147,821,786 , GRCh37.p13 chr4: 148,548,656-148,742,937 MIR4799, ARHGAP10, 4 more genes
    nsv6629552copy number variation1nstd224human GRCh37 chr4: 148,441,569-148,694,658 , GRCh38.p12 chr4: 147,520,417-147,773,507 EDNRA, TMEM184C, 4 more genes
    nsv6393395copy number variation1nstd223human GRCh38 chr4: 147,636,363-147,636,602 , GRCh37.p13 chr4: 148,557,514-148,557,753 TMEM184C, PRMT9
    nsv6387866copy number variation1nstd223human GRCh38 chr4: 147,538,037-147,970,462 , GRCh37.p13 chr4: 148,459,189-148,891,613 LINC02507, EDNRA, 7 more genes
    nsv6386640copy number variation1nstd223human GRCh38 chr4: 147,603,539-147,659,052 , GRCh37.p13 chr4: 148,524,690-148,580,203 TMEM184C, PRMT9
    nsv6385676copy number variation1nstd223human GRCh38 chr4: 147,627,794-147,628,194 , GRCh37.p13 chr4: 148,548,945-148,549,345 TMEM184C
    nsv6315315copy number variation1nstd102humanUncertain significance GRCh38 chr4: 147,494,740-148,399,180 , GRCh37.p13 chr4: 148,415,892-149,320,332 MIR4799, NR3C2, 10 more genes
    nsv6313618copy number variation1nstd102humanUncertain significance GRCh37 chr4: 148,378,902-148,750,802 , GRCh38.p12 chr4: 147,457,750-147,829,651 ARHGAP10, RN7SL254P, 8 more genes
    nsv6313550copy number variation1nstd102humanUncertain significance GRCh37 chr4: 148,011,767-148,800,454 , GRCh38.p12 chr4: 147,090,615-147,879,303 EDNRA, LINC02507, 11 more genes
    nsv6311715copy number variation1nstd102humanPathogenic GRCh37 chr4: 146,560,292-149,358,012 , GRCh38.p12 chr4: 145,639,140-148,436,860 PRMT5P1, LOC105377472, 32 more genes
    nsv6157552copy number variation1nstd214human GRCh38 chr4: 147,627,905-147,628,024 , GRCh37.p13 chr4: 148,549,056-148,549,175 TMEM184C
    nsv6154631copy number variation1nstd214human GRCh38 chr4: 147,624,329-147,624,418 , GRCh37.p13 chr4: 148,545,480-148,545,569 TMEM184C
    nsv6135297copy number variation1nstd213human GRCh37 chr4: 148,450,000-155,050,001 , GRCh38.p12 chr4: 147,528,848-154,128,849 ANXA2P1, ASS1P8, 86 more genes
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