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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919184copy number variation1nstd209human GRCh38 chr7: 149,264,634-149,267,554 , GRCh37.p13 chr7: 148,961,725-148,964,645 ZNF783
    nsv5859145copy number variation1nstd209human GRCh38 chr7: 149,264,758-149,267,761 , GRCh37.p13 chr7: 148,961,849-148,964,852 ZNF783
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv4951196copy number variation1nstd200human GRCh38 chr7: 149,260,252-149,261,994 , GRCh37.p13 chr7: 148,957,343-148,959,085 ZNF783
    nsv4737065copy number variation1nstd199human GRCh37 chr7: 148,977,170-148,977,222 , GRCh38.p12 chr7: 149,280,079-149,280,131 ZNF783
    nsv4685723copy number variation1nstd102humannot provided GRCh37 chr7: 147,897,705-149,874,566 , GRCh38.p12 chr7: 148,200,613-150,177,477 CUL1, RNY1, 63 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
    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
    nsv4496312mobile element insertion1nstd166human GRCh37.p13 chr7: 148,968,810-148,968,810 , GRCh38.p12 chr7: 149,271,719-149,271,719 ZNF783
    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
    nsv4452353copy number variation1nstd102humannot provided GRCh37 chr7: 147,897,705-149,874,566 , GRCh38.p12 chr7: 148,200,613-150,177,477 RN7SL569P, ZNF746, 63 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
    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
    nsv3924350copy number variation1nstd102humanPathogenic GRCh37 chr7: 145,397,037-159,089,306 , GRCh38 chr7: 145,699,944-159,296,617 , NCBI36 chr7: 145,027,970-158,782,067 LOC107986750, LOC107986856, 237 more genes
    nsv3923788copy number variation1nstd102humanPathogenic GRCh38 chr7: 147,144,002-159,327,017 , NCBI36 chr7: 146,472,027-158,812,468 , GRCh37 chr7: 146,841,094-159,119,707 LOC105375582, RPL36AP28, 235 more genes
    nsv3923268copy number variation1nstd102humanPathogenic NCBI36 chr7: 146,112,671-158,821,424 , GRCh37.p13 chr7: 146,481,738-159,128,663 , GRCh38.p12 chr7: 146,784,646-159,335,973 AOC1, LOC105375602, 236 more genes
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