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Items: 1 to 20 of 68

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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
    nsv4955369copy number variation1nstd200human GRCh38 chr7: 11,253,828-11,272,672 , GRCh37.p13 chr7: 11,293,455-11,312,299 , NPM1P11
    nsv4955364copy number variation1nstd200human GRCh38 chr7: 11,191,524-11,262,359 , GRCh37.p13 chr7: 11,231,151-11,301,986 , 1 more genes
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4729635copy number variation1nstd102humanLikely benign GRCh37 chr7: 10,528,678-11,457,492 , GRCh38.p12 chr7: 10,489,051-11,417,865 NDUFA4, LOC100131472, 7 more genes
    nsv4729065copy number variation1nstd102humanUncertain significance GRCh37 chr7: 10,712,710-11,500,366 , GRCh38.p12 chr7: 10,673,083-11,460,739 PHF14, LOC100131472, 7 more genes
    nsv4675835copy number variation1nstd102humanUncertain significance GRCh37 chr7: 10,116,563-11,737,690 , GRCh38.p12 chr7: 10,076,936-11,698,063 PHF14, LOC107986766, 12 more genes
    nsv4618647copy number variation1nstd183human GRCh37 chr7: 10,276,673-11,803,023 , GRCh38.p12 chr7: 10,237,046-11,763,397 , LOC107986766, 12 more genes
    nsv4456827copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,376-19,520,619 , GRCh38.p12 chr7: 43,376-19,480,996 MIR6836, EEF1A1P26, 277 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
    nsv4395030copy number variation1nstd174human GRCh37 chr7: 10,279,486-11,796,901 , GRCh38.p12 chr7: 10,239,859-11,757,275 , NPM1P11, 12 more genes
    nsv4151646copy number variation1nstd166human GRCh37.p13 chr7: 10,632,576-11,385,620 , GRCh38.p12 chr7: 10,592,949-11,345,993 , NDUFA4, 8 more genes
    nsv4140930copy number variation1nstd166human GRCh37.p13 chr7: 10,862,932-11,569,139 , GRCh38.p12 chr7: 10,823,305-11,529,512 , NDUFA4, 6 more genes
    nsv4133664copy number variation1nstd166human GRCh37.p13 chr7: 10,711,050-11,496,845 , GRCh38.p12 chr7: 10,671,423-11,457,218 , NPM1P11, 9 more genes
    nsv3924019copy number variation1nstd102humanLikely benign NCBI36 chr7: 10,841,942-11,529,208 , GRCh37 chr7: 10,875,417-11,562,683 , GRCh38 chr7: 10,835,790-11,523,056 NPM1P11, RPL23AP52, 4 more genes
    nsv3923125copy number variation1nstd102humanPathogenic GRCh38 chr7: 11,122,492-16,479,303 , NCBI36 chr7: 11,128,644-16,485,453 , GRCh37 chr7: 11,162,119-16,518,928 THRAP3P3, ETV1, 43 more genes
    nsv3922329copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-27,236,023 , GRCh38 chr7: 43,360-27,196,404 , NCBI36 chr7: 138,443-27,202,548 LOC401312, IQCE, 411 more genes
    nsv3921823copy number variation1nstd102humanUncertain significance NCBI36 chr7: 10,112,610-11,720,960 , GRCh37 chr7: 10,146,085-11,754,435 , GRCh38 chr7: 10,106,458-11,714,808 PHF14, LOC100131472, 12 more genes
    nsv3921123copy number variation1nstd102humanUncertain significance GRCh38 chr7: 10,691,723-11,375,132 , GRCh37 chr7: 10,731,350-11,414,759 , NCBI36 chr7: 10,697,875-11,381,284 LOC107986767, NDUFA4, 6 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
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