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Items: 1 to 20 of 184

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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
    nsv5918112copy number variation1nstd209human GRCh38 chr7: 150,572,843-150,573,034 , GRCh37.p13 chr7: 150,269,931-150,270,122 GIMAP4
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 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
    nsv4683136copy number variation1nstd102humanPathogenic GRCh37 chr7: 150,066,801-150,759,750 , GRCh38.p12 chr7: 150,369,712-151,062,663 ALDH7A1P3, GIMAP8, 32 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
    nsv4601411copy number variation1nstd183human GRCh37 chr7: 150,249,312-150,312,843 , GRCh38.p12 chr7: 150,552,224-150,615,755 GIMAP4, EIF2AP2, 2 more genes
    nsv4599359copy number variation1nstd183human GRCh37 chr7: 150,171,663-150,285,801 , GRCh38.p12 chr7: 150,474,575-150,588,713 ALDH7A1P3, GIMAP4, 5 more genes
    nsv4479241mobile element insertion1nstd166human GRCh37.p13 chr7: 150,265,860-150,265,860 , GRCh38.p12 chr7: 150,568,772-150,568,772 GIMAP4
    nsv4457333copy number variation1nstd102humanUncertain significance GRCh37 chr7: 150,112,013-150,707,556 , GRCh38.p12 chr7: 150,414,925-151,010,468 TRPC6P3, GIMAP4, 24 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
    nsv4167644copy number variation1nstd166human GRCh37.p13 chr7: 150,255,776-150,400,912 , GRCh38.p12 chr7: 150,558,688-150,703,824 GIMAP2, GIMAP4, 5 more genes
    nsv4164659copy number variation1nstd166human GRCh37.p13 chr7: 150,263,376-150,269,217 , GRCh38.p12 chr7: 150,566,288-150,572,129 GIMAP4
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