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Items: 1 to 20 of 224

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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
    nsv7054149inversion1nstd229human GRCh38 chr4: 79,216,923-83,461,355 , GRCh37.p13 chr4: 80,138,077-84,382,508 RNU6-615P, ANTXR2, 63 more genes
    nsv7049185inversion1nstd229human GRCh38 chr4: 77,808,799-83,184,403 , GRCh37.p13 chr4: 78,729,953-84,105,556 VAMP9P, HNRNPA3P13, 75 more genes
    nsv6756048copy number variation1nstd229human GRCh38 chr4: 82,903,378-82,904,294 , GRCh37.p13 chr4: 83,824,531-83,825,447 THAP9
    nsv6754853copy number variation1nstd229human GRCh38 chr4: 82,910,601-82,962,300 , GRCh37.p13 chr4: 83,831,754-83,883,453 THAP9, LIN54
    nsv6752211copy number variation1nstd229human GRCh38 chr4: 82,904,932-82,914,909 , GRCh37.p13 chr4: 83,826,085-83,836,062 THAP9
    nsv6748172copy number variation1nstd229human GRCh38 chr4: 82,906,975-82,924,480 , GRCh37.p13 chr4: 83,828,128-83,845,633 THAP9, LIN54
    nsv6742138copy number variation1nstd229human GRCh38 chr4: 82,533,814-82,964,129 , GRCh37.p13 chr4: 83,454,967-83,885,282 THAP9, MIR575, 10 more genes
    nsv6565136inversion1nstd223human GRCh38 chr4: 74,413,523-83,001,891 , GRCh37.p13 chr4: 75,279,240-83,923,044 RNU6-615P, SHROOM3, 144 more genes
    nsv6393382copy number variation1nstd223human GRCh38 chr4: 82,898,101-82,900,100 , GRCh37.p13 chr4: 83,819,254-83,821,253 THAP9, SEC31A, 2 more genes
    nsv6381230copy number variation1nstd223human GRCh38 chr4: 82,903,403-82,904,262 , GRCh37.p13 chr4: 83,824,556-83,825,415 THAP9
    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
    nsv6291017copy number variation1nstd102humanUncertain significance GRCh37 chr4: 83,402,855-83,847,970 , GRCh38.p12 chr4: 82,481,702-82,926,817 PTPN11P5, LIN54, 12 more genes
    nsv6135617copy number variation1nstd213human GRCh37 chr4: 83,540,000-83,890,001 , GRCh38.p12 chr4: 82,618,847-82,968,848 SEC31A, THAP9, 8 more genes
    nsv6135364copy number variation1nstd213human GRCh37 chr4: 83,720,000-84,190,001 , GRCh38.p12 chr4: 82,798,847-83,268,848 SEC31A, COQ2, 10 more genes
    nsv6119067copy number variation1nstd186human GRCh37 chr4: 83,824,549-83,825,448 , GRCh38.p12 chr4: 82,903,396-82,904,295 THAP9
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