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Items: 1 to 20 of 97

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5719973mobile element insertion2nstd211human GRCh38 chr7: 54,934,852-54,934,852 , GRCh37.p13 chr7: 55,002,545-55,002,545 LOC643168
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5556396mobile element insertion1nstd206human GRCh38 chr7: 54,934,852-54,934,903 , GRCh37.p13 chr7: 55,002,545-55,002,596 LOC643168
    nsv5119606mobile element insertion1nstd203human GRCh38 chr7: 54,939,190-54,939,204 , GRCh37.p13 chr7: 55,006,883-55,006,897 LOC643168
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4953710copy number variation1nstd200human GRCh38 chr7: 54,583,600-55,152,153 , GRCh37.p13 chr7: 54,651,293-55,219,846 SEC61G, SEC61G-DT, 5 more genes
    nsv4828951copy number variation1nstd200human GRCh37 chr7: 54,651,293-55,219,846 , GRCh38.p12 chr7: 54,583,600-55,152,153 EGFR, LOC643168, 5 more genes
    nsv4713309copy number variation1nstd195human GRCh37 chr7: 54,992,851-55,234,301 , GRCh38.p12 chr7: 54,925,158-55,166,608 EGFR, LOC643168, 1 more genes
    nsv4701683copy number variation1nstd195human GRCh37 chr7: 54,993,101-55,015,601 , GRCh38.p12 chr7: 54,925,408-54,947,908 LOC643168
    nsv4562173mobile element insertion1nstd166human GRCh37.p13 chr7: 55,002,528-55,002,528 , GRCh38.p12 chr7: 54,934,835-54,934,835 LOC643168
    nsv4457295copy number variation1nstd102humanUncertain significance GRCh37 chr7: 54,644,022-55,165,236 , GRCh38.p12 chr7: 54,576,329-55,097,543 RNU6-1125P, SEC61G, 5 more genes
    nsv4456853copy number variation1nstd102humanUncertain significance GRCh37 chr7: 54,651,292-55,220,177 , GRCh38.p12 chr7: 54,583,599-55,152,484 RPL31P35, RNU6-1125P, 5 more genes
    nsv4455806copy number variation1nstd102humanUncertain significance GRCh37 chr7: 52,809,787-58,025,873 , GRCh38.p12 chr7: 52,742,093-57,966,167 RPL31P35, SEC61G, 161 more genes
    nsv4455283copy number variation1nstd102humanUncertain significance GRCh37 chr7: 54,642,138-55,164,200 , GRCh38.p12 chr7: 54,574,445-55,096,507 EGFR, LOC643168, 5 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
    nsv4393794copy number variation1nstd174human GRCh37 chr7: 54,641,984-55,219,182 , GRCh38.p12 chr7: 54,574,291-55,151,489 EGFR, SEC61G, 5 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv4151732copy number variation1nstd166human GRCh37.p13 chr7: 54,651,293-55,219,856 , GRCh38.p12 chr7: 54,583,600-55,152,163 EGFR, SEC61G, 5 more genes
    nsv3924054copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,573,756-56,174,815 , NCBI36 chr7: 40,540,281-56,142,309 , GRCh38 chr7: 40,534,157-56,107,122 VOPP1-DT, SGO1P2, 229 more genes
    nsv3922900copy number variation1nstd102humanUncertain significance GRCh37 chr7: 52,260,224-57,882,999 , NCBI36 chr7: 52,227,718-57,886,941 , GRCh38 chr7: 52,192,528-57,823,293 LOC102723656, LOC728376, 160 more genes
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