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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6995435copy number variation1nstd229human GRCh38 chr17: 76,542,220-76,720,249 , GRCh37.p13 chr17: 74,538,302-74,716,331 SNORD1B, PTMAP13, 12 more genes
    nsv6992470copy number variation1nstd229human GRCh38 chr17: 76,503,294-76,561,168 , GRCh37.p13 chr17: 74,499,376-74,557,250 SNORD1B, CYGB, 4 more genes
    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
    nsv6982022copy number variation1nstd229human GRCh38 chr17: 76,559,952-76,577,945 , GRCh37.p13 chr17: 74,556,034-74,574,027 SNORD1B, SNHG16, 2 more genes
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6533699copy number variation1nstd223human GRCh38 chr17: 76,561,806-76,564,665 , GRCh37.p13 chr17: 74,557,888-74,560,747 SNHG16, SNORD1A, 1 more genes
    nsv6519734copy number variation1nstd223human GRCh38 chr17: 76,564,368-76,577,863 , GRCh37.p13 chr17: 74,560,450-74,573,945 ST6GALNAC2, SNHG16
    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
    nsv6037641copy number variation1nstd212human GRCh38 chr17: 76,563,878-76,564,217 , GRCh37.p13 chr17: 74,559,960-74,560,299 ST6GALNAC2, SNHG16
    nsv5930720copy number variation1nstd209human GRCh38 chr17: 76,563,878-76,564,216 , GRCh37.p13 chr17: 74,559,960-74,560,298 ST6GALNAC2, SNHG16
    nsv5533807copy number variation1nstd206human GRCh38 chr17: 76,563,863-76,564,227 , GRCh37.p13 chr17: 74,559,945-74,560,309 SNHG16, ST6GALNAC2
    nsv5525355copy number variation1nstd206human GRCh38 chr17: 76,550,542-76,584,098 , GRCh37.p13 chr17: 74,546,624-74,580,180 ST6GALNAC2, CYGB, 5 more genes
    nsv5514371copy number variation1nstd206human GRCh38 chr17: 76,565,433-76,565,520 , GRCh37.p13 chr17: 74,561,515-74,561,602 SNHG16, ST6GALNAC2
    nsv5349681translocation1nstd200human GRCh38 chr17: 76,565,433-76,565,433 , GRCh38 chr17: 76,565,520-76,565,520 , GRCh37.p13 chr17: 74,561,515-74,561,515 , GRCh37.p13 chr17: 74,561,602-74,561,602 SNHG16, ST6GALNAC2
    nsv5333170translocation1nstd200human GRCh37 chr17: 74,561,602-74,561,602 , GRCh37 chr17: 74,561,515-74,561,515 , GRCh38.p12 chr17: 76,565,520-76,565,520 , GRCh38.p12 chr17: 76,565,433-76,565,433 SNHG16, ST6GALNAC2
    nsv5320487translocation1nstd204human GRCh37.p13 chr17: 74,561,602-74,561,602 , GRCh37.p13 chr17: 74,561,515-74,561,515 , GRCh38.p13 chr17: 76,565,520-76,565,520 , GRCh38.p13 chr17: 76,565,433-76,565,433 ST6GALNAC2, SNHG16
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
    nsv5158082mobile element insertion1nstd203human GRCh38 chr17: 76,562,481-76,562,506 , GRCh37.p13 chr17: 74,558,563-74,558,588 SNHG16
    nsv5016760copy number variation1nstd200human GRCh38 chr17: 76,556,197-76,556,763 , GRCh37.p13 chr17: 74,552,279-74,552,845 SNHG16, CYGB
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