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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5258059copy number variation1nstd204human GRCh37.p13 chr7: 148,640,893-148,818,092 , GRCh38.p13 chr7: 148,943,801-149,121,000 RNY1, RNY3, 7 more genes
    nsv5196245mobile element insertion1nstd203human GRCh38 chr7: 148,989,855-148,989,867 , GRCh37.p13 chr7: 148,686,947-148,686,959 GHET1
    nsv5190379mobile element insertion1nstd203human GRCh38 chr7: 148,989,848-148,989,867 , GRCh37.p13 chr7: 148,686,940-148,686,959 GHET1
    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
    nsv4561363mobile element insertion1nstd166human GRCh37.p13 chr7: 148,686,940-148,686,940 , GRCh38.p12 chr7: 148,989,848-148,989,848 GHET1
    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
    nsv4388255copy number variation1nstd173human GRCh37 chr7: 147,732,649-148,920,690 , GRCh38.p12 chr7: 148,035,557-149,223,598 ZNF786, RNY1, 26 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
    nsv4157757copy number variation1nstd166human GRCh37.p13 chr7: 148,684,353-148,684,534 , GRCh38.p12 chr7: 148,987,261-148,987,442 RNY1, GHET1
    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
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