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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5891703copy number variation1nstd209human GRCh38 chr4: 177,441,170-177,441,979 , GRCh37.p13 chr4: 178,362,324-178,363,133 AGA-DT, AGA
    nsv5673742copy number variation1nstd102humanPathogenic GRCh37 chr4: 178,363,393-178,363,667 , GRCh38.p12 chr4: 177,442,239-177,442,513 AGA-DT, AGA
    nsv5642706insertion1nstd207human GRCh38 chr4: 177,439,722-177,439,722 , GRCh37.p13 chr4: 178,360,876-178,360,876 AGA
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5469668copy number variation1nstd206human GRCh38 chr4: 177,440,884-177,444,453 , GRCh37.p13 chr4: 178,362,038-178,365,607 AGA-DT, AGA
    nsv5463487copy number variation1nstd206human GRCh38 chr4: 177,208,588-178,945,069 , GRCh37.p13 chr4: 178,129,742-179,866,223 NEIL3, RPL19P8, 14 more genes
    nsv5459568copy number variation1nstd206human GRCh38 chr4: 177,441,174-177,441,980 , GRCh37.p13 chr4: 178,362,328-178,363,134 AGA-DT, AGA
    nsv5362008translocation1nstd200human GRCh38 chr4: 177,436,576-177,436,576 , GRCh38 chr4: 177,436,502-177,436,502 , GRCh37.p13 chr4: 178,357,656-178,357,656 , GRCh37.p13 chr4: 178,357,730-178,357,730 AGA
    nsv5345292translocation1nstd200human GRCh37 chr4: 178,360,014-178,360,014 , GRCh37 chr4: 178,360,729-178,360,729 , GRCh38.p12 chr4: 177,438,860-177,438,860 , GRCh38.p12 chr4: 177,439,575-177,439,575 AGA
    nsv5326249translocation1nstd204human GRCh38.p13 chr4: 177,438,860-177,438,860 , GRCh38.p13 chr4: 177,439,575-177,439,575 , GRCh37.p13 chr4: 178,360,729-178,360,729 , GRCh37.p13 chr4: 178,360,014-178,360,014 AGA
    nsv4944076copy number variation1nstd200human GRCh38 chr4: 177,438,202-177,438,360 , GRCh37.p13 chr4: 178,359,356-178,359,514 AGA
    nsv4930171copy number variation1nstd200human GRCh38 chr4: 177,441,174-177,441,980 , GRCh37.p13 chr4: 178,362,328-178,363,134 AGA, AGA-DT
    nsv4930170copy number variation1nstd200human GRCh38 chr4: 177,440,534-177,441,515 , GRCh37.p13 chr4: 178,361,688-178,362,669 AGA, AGA-DT
    nsv4801864copy number variation1nstd200human GRCh37 chr4: 178,362,328-178,363,134 , GRCh38.p12 chr4: 177,441,174-177,441,980 AGA, AGA-DT
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4729585copy number variation1nstd102humanLikely benign GRCh37 chr4: 177,958,066-178,698,605 , GRCh38.p12 chr4: 177,036,912-177,777,451 AGA, LOC105377560, 8 more genes
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