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Items: 1 to 20 of 173

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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
    nsv5912840copy number variation1nstd209human GRCh38 chr7: 151,162,480-151,188,779 , GRCh37.p13 chr7: 150,859,567-150,885,866 GBX1, ASB10
    nsv5860368copy number variation1nstd209human GRCh38 chr7: 151,173,742-151,175,341 , GRCh37.p13 chr7: 150,870,829-150,872,428 ASB10
    nsv5852171copy number variation1nstd209human GRCh38 chr7: 151,162,169-151,174,941 , GRCh37.p13 chr7: 150,859,256-150,872,028 GBX1, ASB10
    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
    nsv5378898translocation1nstd200human GRCh38 chr7: 151,310,504-151,310,504 , GRCh38 chr7: 151,180,823-151,180,823 , GRCh37.p13 chr7: 150,877,910-150,877,910 , GRCh37.p13 chr7: 151,007,590-151,007,590 ASB10
    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
    nsv4951261copy number variation1nstd200human GRCh38 chr7: 151,184,368-151,189,145 , GRCh37.p13 chr7: 150,881,455-150,886,232 ASB10, IQCA1L
    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
    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
    nsv4608602copy number variation1nstd183human GRCh37 chr7: 150,883,272-150,884,136 , GRCh38.p12 chr7: 151,186,185-151,187,049 ASB10
    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
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