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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979093inversion1nstd209human GRCh38 chr7: 150,023,235-154,074,108 , GRCh37.p13 chr7: 149,720,324-153,771,193 , AOC1, 98 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5381637copy number variation1nstd102humanUncertain significance GRCh37 chr7: 150,642,453-152,373,165 , GRCh38.p12 chr7: 150,945,365-152,676,080 WDR86-AS1, XRCC2, 44 more genes
    nsv5248297copy number variation1nstd204human GRCh38.p13 chr7: 151,432,839-151,434,138 , GRCh37.p13 chr7: 151,129,925-151,131,224 CRYGN, MIR3907
    nsv4954075copy number variation1nstd200human GRCh38 chr7: 151,139,481-151,761,662 , GRCh37.p13 chr7: 150,836,568-151,458,748 ABCF2-H2BK1, MIR3907, 17 more genes
    nsv4754093inversion1nstd199human GRCh37 chr7: 149,731,009-153,760,532 , GRCh38.p12 chr7: 150,033,920-154,063,447 , AOC1, 98 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
    nsv4683838copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr7: 150,642,443-151,385,353 , GRCh38.p12 chr7: 150,945,355-151,688,267 CDK5, MIR3907, 26 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
    nsv4675539copy number variation1nstd102humanUncertain significance GRCh37 chr7: 151,093,231-151,402,949 , GRCh38.p12 chr7: 151,396,145-151,705,863 WDR86, RN7SL76P, 6 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
    nsv4457130copy number variation1nstd102humanUncertain significance GRCh37 chr7: 149,968,222-152,539,376 , GRCh38.p12 chr7: 150,271,133-152,842,291 REPIN1, XRCC2, 80 more genes
    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
    nsv4381716copy number variation1nstd173human GRCh37 chr7: 146,525,217-159,119,707 , GRCh38.p12 chr7: 146,828,125-159,327,017 , TRC-GCA17-1, 247 more genes
    nsv4349183copy number variation1nstd102humanPathogenic GRCh37 chr7: 128,312,450-159,119,220 , GRCh38.p12 chr7: 128,672,396-159,326,530 LOC105375582, TRBJ2-4, 686 more genes
    nsv3971439inversion1nstd168human GRCh38 chr7: 149,962,989-154,150,884 , GRCh37.p13 chr7: 149,660,078-153,847,969 , AOC1, 98 more genes
    nsv3970573inversion1nstd168human GRCh38 chr7: 149,903,084-154,133,979 , GRCh37.p13 chr7: 149,600,173-153,831,064 , AOC1, 98 more genes
    nsv3924585copy number variation1nstd102humanPathogenic NCBI36 chr7: 130,506,777-158,812,468 , GRCh38 chr7: 131,171,478-159,327,017 , GRCh37 chr7: 130,856,237-159,119,707 PAXBP1P1, RNY3, 611 more genes
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