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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5710159mobile element insertion1nstd211human GRCh38 chr7: 155,642,129-155,642,129 , GRCh37.p13 chr7: 155,434,823-155,434,823 RBM33-DT
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5477961copy number variation1nstd206human GRCh38 chr7: 155,642,651-155,643,401 , GRCh37.p13 chr7: 155,435,345-155,436,095 RBM33-DT, RBM33
    nsv5407994mobile element insertion1nstd206human GRCh38 chr7: 155,642,129-155,642,180 , GRCh37.p13 chr7: 155,434,823-155,434,874 RBM33-DT
    nsv5304455copy number variation1nstd204human GRCh38.p13 chr7: 155,633,432-155,646,126 , GRCh37.p13 chr7: 155,426,126-155,438,820 RBM33, RBM33-DT
    nsv5259305copy number variation1nstd204human GRCh38.p13 chr7: 155,633,401-155,646,100 , GRCh37.p13 chr7: 155,426,095-155,438,794 RBM33, RBM33-DT
    nsv5252585copy number variation1nstd204human GRCh38.p13 chr7: 155,631,319-155,645,998 , GRCh37.p13 chr7: 155,424,013-155,438,692 RBM33-DT, RBM33
    nsv4954141copy number variation1nstd200human GRCh38 chr7: 155,630,184-155,762,738 , GRCh37.p13 chr7: 155,422,878-155,555,432 RBM33, RBM33-DT
    nsv4825469copy number variation1nstd200human GRCh37 chr7: 155,426,150-155,438,798 , GRCh38.p12 chr7: 155,633,456-155,646,104 RBM33, RBM33-DT
    nsv4729251copy number variation1nstd102humanPathogenic GRCh37 chr7: 152,800,000-159,138,663 , GRCh38.p12 chr7: 153,102,915-159,335,973 LOC105375597, LOC105375577, 81 more genes
    nsv4728807copy number variation1nstd102humanPathogenic GRCh37 chr7: 155,319,280-159,119,707 , GRCh38.p12 chr7: 155,526,585-159,327,017 RBM33, LOC645272, 50 more genes
    nsv4685715copy number variation1nstd102humannot provided GRCh37 chr7: 143,107,740-156,886,246 , GRCh38.p12 chr7: 143,410,647-157,093,552 CTAGE4, CDK5, 277 more genes
    nsv4684261copy number variation1nstd102humanUncertain significance GRCh37 chr7: 154,585,431-155,488,931 , GRCh38.p12 chr7: 154,793,721-155,696,237 LOC105375593, INSIG1, 21 more genes
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4675615copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620 ATG9B, OR10AC1, 603 more genes
    nsv4675268copy number variation1nstd102humanPathogenic GRCh37 chr7: 145,962,558-159,119,707 , GRCh38.p12 chr7: 146,265,466-159,327,017 ABCB8, THAP5P1, 237 more genes
    nsv4489170mobile element insertion1nstd166human GRCh37.p13 chr7: 155,434,809-155,434,809 , GRCh38.p12 chr7: 155,642,115-155,642,115 RBM33-DT
    nsv4455493copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,592,554-159,119,707 , GRCh38.p12 chr7: 130,907,795-159,327,017 OR2A1, LOC101027084, 614 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4386491copy number variation1nstd173human GRCh37 chr7: 155,411,695-155,538,800 , GRCh38.p12 chr7: 155,619,001-155,746,106 RBM33, RBM33-DT
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