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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052940inversion1nstd229human GRCh38 chr4: 73,455,263-76,320,440 , GRCh37.p13 chr4: 74,320,980-77,241,593 , RASSF6, 65 more genes
    nsv7051783inversion1nstd229human GRCh38 chr4: 75,524,259-75,536,088 , GRCh37.p13 chr4: 76,449,469-76,461,298 THAP6
    nsv7045939inversion1nstd229human GRCh38 chr4: 69,867,306-75,844,103 , GRCh37.p13 chr4: 70,733,024-76,765,256 , PF4V1, 99 more genes
    nsv7040415inversion1nstd229human GRCh38 chr4: 72,183,424-80,893,316 , GRCh37.p13 chr4: 73,049,141-81,814,470 , KPNA2P1, 148 more genes
    nsv6755982copy number variation1nstd229human GRCh38 chr4: 75,546,847-75,554,562 , GRCh37.p13 chr4: 76,472,057-76,479,772 THAP6, ODAPH
    nsv6750761copy number variation1nstd229human GRCh38 chr4: 75,529,653-75,569,099 , GRCh37.p13 chr4: 76,454,863-76,494,309 THAP6, ODAPH
    nsv6749244copy number variation1nstd229human GRCh38 chr4: 71,830,854-79,510,197 , GRCh37.p13 chr4: 72,696,571-80,431,351 , COX18, 134 more genes
    nsv6746144copy number variation1nstd229human GRCh38 chr4: 75,539,514-75,539,927 , GRCh37.p13 chr4: 76,464,724-76,465,137 THAP6
    nsv6744597copy number variation1nstd229human GRCh38 chr4: 75,528,446-75,532,588 , GRCh37.p13 chr4: 76,453,656-76,457,798 THAP6
    nsv6565136inversion1nstd223human GRCh38 chr4: 74,413,523-83,001,891 , GRCh37.p13 chr4: 75,279,240-83,923,044 RNU6-615P, SHROOM3, 144 more genes
    nsv6383868copy number variation1nstd223human GRCh38 chr4: 75,528,443-75,532,587 , GRCh37.p13 chr4: 76,453,653-76,457,797 THAP6
    nsv6314916copy number variation1nstd102humanPathogenic GRCh38 chr4: 67,833,055-82,716,065 , GRCh37.p13 chr4: 68,698,773-83,637,218 MICOS10P4, SULT1B1, 274 more genes
    nsv6313802copy number variation1nstd102humanUncertain significance GRCh37 chr4: 75,876,865-76,546,874 , GRCh38.p12 chr4: 74,951,655-75,621,690 THAP6, LOC107986230, 10 more genes
    nsv6313715copy number variation1nstd102humanPathogenic GRCh37 chr4: 73,055,313-80,083,154 , GRCh38.p12 chr4: 72,189,596-79,162,000 CCNG2, FTLP9, 129 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
    nsv6295722copy number variation1nstd186human GRCh37 chr4: 76,455,751-76,456,340 , GRCh38.p12 chr4: 75,530,541-75,531,130 THAP6
    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
    nsv6291068copy number variation1nstd102humanUncertain significance GRCh37 chr4: 75,617,591-76,926,681 , GRCh38.p12 chr4: 74,692,381-76,005,528 LOC105377282, PPEF2, 25 more genes
    nsv6135611copy number variation1nstd213human GRCh37 chr4: 76,190,000-77,120,001 , GRCh38.p12 chr4: 75,264,790-76,198,848 ART3, SCARB2, 21 more genes
    nsv6135361copy number variation1nstd213human GRCh37 chr4: 76,430,000-77,550,001 , GRCh38.p12 chr4: 75,504,790-76,628,848 ART3, SCARB2, 32 more genes
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