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Items: 1 to 20 of 285

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141737copy number variation1nstd232human GRCh37.p13 chr17: 74,394,464-74,394,551 , GRCh38.p12 chr17: 76,398,383-76,398,470 UBE2O
    nsv6994257copy number variation1nstd229human GRCh38 chr17: 76,174,168-76,511,387 , GRCh37.p13 chr17: 74,170,249-74,507,469 RNF157, UBE2O, 12 more genes
    nsv6989133copy number variation1nstd229human GRCh38 chr17: 76,409,641-76,411,930 , GRCh37.p13 chr17: 74,405,723-74,408,012 UBE2O
    nsv6989067copy number variation1nstd229human GRCh38 chr17: 76,416,184-76,416,250 , GRCh37.p13 chr17: 74,412,266-74,412,332 UBE2O
    nsv6986245copy number variation1nstd229human GRCh38 chr17: 76,433,979-76,436,824 , GRCh37.p13 chr17: 74,430,061-74,432,906 UBE2O
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6982239copy number variation1nstd229human GRCh38 chr17: 76,224,241-77,998,670 , GRCh37.p13 chr17: 74,220,322-75,994,751 MFSD11, PRPSAP1, 59 more genes
    nsv6981842copy number variation1nstd229human GRCh38 chr17: 76,430,528-76,433,395 , GRCh37.p13 chr17: 74,426,610-74,429,477 UBE2O, RPL7P49
    nsv6581964inversion1nstd223human GRCh38 chr17: 76,429,020-76,429,559 , GRCh37.p13 chr17: 74,425,102-74,425,641 RPL7P49, UBE2O
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6531718copy number variation1nstd223human GRCh38 chr17: 76,452,101-76,453,600 , GRCh37.p13 chr17: 74,448,183-74,449,682 UBE2O, AANAT
    nsv6528159copy number variation1nstd223human GRCh38 chr17: 76,294,001-76,409,700 , GRCh37.p13 chr17: 74,290,082-74,405,782 UBE2O, HMGN2P43, 4 more genes
    nsv6526261copy number variation1nstd223human GRCh38 chr17: 76,447,464-76,448,072 , GRCh37.p13 chr17: 74,443,546-74,444,154 UBE2O
    nsv6525103copy number variation1nstd223human GRCh38 chr17: 76,409,641-76,411,930 , GRCh37.p13 chr17: 74,405,723-74,408,012 UBE2O
    nsv6521414copy number variation1nstd223human GRCh38 chr17: 76,450,871-76,464,649 , GRCh37.p13 chr17: 74,446,953-74,460,731 AANAT, UBE2O
    nsv6518373copy number variation1nstd223human GRCh38 chr17: 76,425,715-76,426,270 , GRCh37.p13 chr17: 74,421,797-74,422,352 UBE2O
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6314298complex chromosomal rearrangement2nstd102humanUncertain significance GRCh37 chr17: 74,405,340-74,405,340 , GRCh37 chr17: 74,405,346-74,405,346 , GRCh38.p12 chr17: 76,409,258-76,409,258 , GRCh38.p12 chr17: 76,409,264-76,409,264 , GRCh37 chr11: 61,999,067-61,999,067 , GRCh37 chr11: 61,999,068-61,999,068 , GRCh38.p12 chr11: 62,231,595-62,231,595 , GRCh38.p12 chr11: 62,231,596-62,231,596 UBE2O
    nsv6259083mobile element insertion1nstd215human GRCh38 chr17: 76,414,345-76,414,345 , GRCh37.p13 chr17: 74,410,427-74,410,427 UBE2O
    nsv6259082mobile element insertion1nstd215human GRCh38 chr17: 76,389,504-76,389,504 , GRCh37.p13 chr17: 74,385,585-74,385,585 UBE2O
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