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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7053656inversion1nstd229human GRCh38 chr4: 86,694,351-88,137,907 , GRCh37.p13 chr4: 87,615,504-89,059,059 KLHL8, GAPDHP60, 30 more genes
    nsv7050046inversion1nstd229human GRCh38 chr4: 85,500,769-88,545,032 , GRCh37.p13 chr4: 86,421,922-89,466,183 LOC105377326, NUDT9, 54 more genes
    nsv6756249copy number variation1nstd229human GRCh38 chr4: 86,821,071-87,269,326 , GRCh37.p13 chr4: 87,742,224-88,190,478 TECRP1, GAPDHP60, 9 more genes
    nsv6754482copy number variation1nstd229human GRCh38 chr4: 86,873,201-86,955,000 , GRCh37.p13 chr4: 87,794,354-87,876,152 AFF1-AS1, C4orf36, 3 more genes
    nsv6753590copy number variation1nstd229human GRCh38 chr4: 86,763,471-86,911,789 , GRCh37.p13 chr4: 87,684,624-87,832,942 ARPC1AP4, SLC10A6, 3 more genes
    nsv6747792copy number variation1nstd229human GRCh38 chr4: 86,845,822-86,949,508 , GRCh37.p13 chr4: 87,766,975-87,870,660 AFF1-AS1, TECRP1, 5 more genes
    nsv6743165copy number variation1nstd229human GRCh38 chr4: 86,842,201-87,170,600 , GRCh37.p13 chr4: 87,763,354-88,091,752 TECRP1, SLC10A6, 8 more genes
    nsv6742527copy number variation1nstd229human GRCh38 chr4: 86,799,204-86,912,861 , GRCh37.p13 chr4: 87,720,357-87,834,014 RPL6P13, C4orf36, 3 more genes
    nsv6739733copy number variation1nstd229human GRCh38 chr4: 86,861,701-86,958,400 , GRCh37.p13 chr4: 87,782,854-87,879,552 AFF1, TECRP1, 4 more genes
    nsv6629991copy number variation1nstd224human GRCh37 chr4: 87,778,123-87,852,108 , GRCh38.p12 chr4: 86,856,970-86,930,956 AFF1-AS1, C4orf36, 2 more genes
    nsv6379943copy number variation1nstd223human GRCh38 chr4: 86,845,822-86,949,507 , GRCh37.p13 chr4: 87,766,975-87,870,659 AFF1, RPL6P13, 5 more genes
    nsv6313848copy number variation1nstd102humanPathogenic GRCh37 chr4: 81,054,789-90,667,421 , GRCh38.p12 chr4: 80,133,635-89,746,270 RPL6P13, SNORD144, 136 more genes
    nsv6313510copy number variation1nstd102humanPathogenic GRCh37 chr4: 75,737,340-91,131,156 , GRCh38.p12 chr4: 74,812,130-90,210,005 HIGD1AP13, CXCL11, 240 more genes
    nsv6313484copy number variation1nstd102humanPathogenic GRCh37 chr4: 79,780,152-94,873,225 , GRCh38.p12 chr4: 78,858,998-93,952,074 LOC105377329, LOC107986294, 166 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291249copy number variation1nstd102humanPathogenic GRCh37 chr4: 80,467,886-93,362,064 , GRCh38.p12 chr4: 79,546,732-92,440,913 HNRNPA3P13, LOC105377310, 155 more genes
    nsv6135619copy number variation1nstd213human GRCh37 chr4: 87,220,000-88,340,001 , GRCh38.p12 chr4: 86,298,847-87,418,849 GAPDHP60, AFF1, 19 more genes
    nsv5896467copy number variation1nstd209human GRCh38 chr4: 86,411,170-87,486,334 , GRCh37.p13 chr4: 87,332,323-88,407,486 , MIR4452, 21 more genes
    nsv5893925copy number variation1nstd209human GRCh38 chr4: 86,911,448-86,915,709 , GRCh37.p13 chr4: 87,832,601-87,836,862 ARPC1AP4
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