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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5479066copy number variation1nstd206human GRCh38 chr7: 141,970,724-141,972,497 , GRCh37.p13 chr7|NW_003571040.1: 112,675-114,448 , GRCh37.p13 chr7: 141,670,524-141,672,297 TAS2R38
    nsv4614873copy number variation1nstd183human GRCh37 chr7: 141,670,420-141,672,208 , GRCh38.p12 chr7: 141,970,620-141,972,408 TAS2R38
    esv3851661copy number variation1estd219human GRCh37 chr7: 141,670,229-141,672,571 , GRCh38.p12 chr7: 141,970,429-141,972,771 TAS2R38
    esv3615260copy number variation1estd214human GRCh37 chr7: 141,670,229-141,672,571 , GRCh38.p12 chr7: 141,970,429-141,972,771 TAS2R38
    esv2672327copy number variation1estd199human GRCh37 chr7: 141,670,402-141,672,241 , GRCh38.p12 chr7: 141,970,602-141,972,441 TAS2R38
    nsv4494466mobile element insertion1nstd166human GRCh37.p13 chr7: 141,670,604-141,670,604 , GRCh38.p12 chr7: 141,970,804-141,970,804 TAS2R38
    nsv6821567copy number variation1nstd229human GRCh38 chr7: 141,971,001-142,014,000 , GRCh37.p13 chr7: 141,670,801-141,713,800 , GRCh37.p13 chr7|NW_003571040.1: 112,952-155,951 TAS2R38, MGAM
    nsv6631776copy number variation1nstd224human GRCh37 chr7: 141,630,247-141,678,392 , GRCh38.p12 chr7: 141,930,447-141,978,592 TAS2R38, CLEC5A
    nsv6631569copy number variation1nstd224human GRCh37 chr7: 141,629,932-141,673,483 , GRCh38.p12 chr7: 141,930,132-141,973,683 TAS2R38, CLEC5A
    nsv4153373copy number variation1nstd166human GRCh37.p13 chr7: 141,624,000-141,681,000 , GRCh38.p12 chr7: 141,924,200-141,981,200 TAS2R38, CLEC5A
    nsv4606045copy number variation1nstd183human GRCh37 chr7: 141,626,847-141,679,725 , GRCh38.p12 chr7: 141,927,047-141,979,925 TAS2R38, CLEC5A
    nsv524927copy number variation1nstd21human NCBI35 chr7: 141,125,788-141,139,367 , GRCh37.p13 chr7|NW_003571040.1: 114,755-128,334 , GRCh37.p13 chr7: 141,672,604-141,686,183 , GRCh38.p12 chr7: 141,972,804-141,986,383 TAS2R38, MGAM
    nsv3149348copy number variation1nstd151human GRCh37 chr7: 141,635,611-141,759,403 , GRCh38.p12 chr7: 141,935,811-142,059,603 TAS2R38, CLEC5A, 1 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 TAS2R38, RNU6-438P, 2682 more genes
    nsv4675615copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620 TAS2R38, ATG9B, 603 more genes
    nsv3915633copy number variation1nstd102humanPathogenic NCBI36 chr7: 134,002,121-158,077,335 , GRCh38 chr7: 134,666,829-158,591,882 , GRCh37 chr7: 134,351,581-158,384,574 TAS2R38, MOXD2P, 561 more genes
    nsv3897512copy number variation1nstd102humanPathogenic GRCh37 chr7: 137,917,376-159,119,707 , GRCh38.p12 chr7: 138,232,630-159,327,017 TAS2R38, LOC105375548, 520 more genes
    nsv7097864copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959 TAS2R38, NOBOX, 466 more genes
    nsv3903590copy number variation1nstd102humanPathogenic GRCh37 chr7: 140,133,025-158,982,771 , GRCh38.p12 chr7: 140,433,225-159,190,080 TAS2R38, LOC105375597, 468 more genes
    nsv3910344copy number variation1nstd102humanPathogenic GRCh38 chr7: 140,754,198-159,307,523 , GRCh37 chr7: 140,453,998-159,100,212 , NCBI36 chr7: 140,100,467-158,792,973 TAS2R38, LOC112268012, 461 more genes
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