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Items: 1 to 20 of 312

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5917791copy number variation1nstd209human GRCh38 chr10: 114,306,315-114,306,368 , GRCh37.p13 chr10: 116,066,074-116,066,127 AFAP1L2
    nsv5910997copy number variation1nstd209human GRCh38 chr10: 114,345,877-114,345,952 , GRCh37.p13 chr10: 116,105,636-116,105,711 AFAP1L2
    nsv5855705copy number variation1nstd209human GRCh38 chr10: 114,398,972-114,401,271 , GRCh37.p13 chr10: 116,158,731-116,161,030 AFAP1L2
    nsv5730517mobile element insertion1nstd211human GRCh38 chr10: 114,352,090-114,352,090 , GRCh37.p13 chr10: 116,111,849-116,111,849 AFAP1L2
    nsv5624940insertion1nstd207human GRCh38 chr10: 114,306,315-114,306,315 , GRCh37.p13 chr10: 116,066,074-116,066,074 AFAP1L2
    nsv5604438copy number variation1nstd207human GRCh38 chr10: 114,345,856-114,345,931 , GRCh37.p13 chr10: 116,105,615-116,105,690 AFAP1L2
    nsv5555392mobile element insertion1nstd206human GRCh38 chr10: 114,352,090-114,352,104 , GRCh37.p13 chr10: 116,111,849-116,111,863 AFAP1L2
    nsv5341730translocation1nstd200human GRCh37 chr10: 116,153,098-116,153,098 , GRCh37 chr10: 116,153,022-116,153,022 , GRCh38.p12 chr10: 114,393,263-114,393,263 , GRCh38.p12 chr10: 114,393,339-114,393,339 AFAP1L2
    nsv5327857inversion1nstd204human GRCh37.p13 chr10: 115,288,018-116,786,304 , GRCh38.p13 chr10: 113,528,259-115,723,405 , ADRB1, 31 more genes
    nsv5319074copy number variation1nstd204human GRCh38.p13 chr10: 114,297,113-114,301,138 , GRCh37.p13 chr10: 116,056,872-116,060,897 AFAP1L2
    nsv5258465copy number variation1nstd204human GRCh38.p13 chr10: 114,297,201-114,301,100 , GRCh37.p13 chr10: 116,056,960-116,060,859 AFAP1L2
    nsv5253703copy number variation1nstd204human GRCh38.p13 chr10: 114,304,201-114,308,200 , GRCh37.p13 chr10: 116,063,960-116,067,959 AFAP1L2
    nsv5252339copy number variation1nstd204human GRCh38.p13 chr10: 114,297,142-114,301,041 , GRCh37.p13 chr10: 116,056,901-116,060,800 AFAP1L2
    nsv5241764copy number variation1nstd204human GRCh38.p13 chr10: 114,309,099-114,310,498 , GRCh37.p13 chr10: 116,068,858-116,070,257 AFAP1L2
    nsv5127851mobile element insertion1nstd203human GRCh38 chr10: 114,318,747-114,318,747 , GRCh37.p13 chr10: 116,078,506-116,078,506 AFAP1L2, LOC105378494
    nsv5029881inversion1nstd200human GRCh38 chr10: 113,528,269-115,723,396 , GRCh37.p13 chr10: 115,288,028-116,786,295 , NHLRC2, 31 more genes
    nsv4977047copy number variation1nstd200human GRCh38 chr10: 114,348,066-114,349,705 , GRCh37.p13 chr10: 116,107,825-116,109,464 AFAP1L2
    nsv4977046copy number variation1nstd200human GRCh38 chr10: 114,325,198-114,325,400 , GRCh37.p13 chr10: 116,084,957-116,085,159 LOC105378494, AFAP1L2
    nsv4977045copy number variation1nstd200human GRCh38 chr10: 114,324,573-114,328,548 , GRCh37.p13 chr10: 116,084,332-116,088,307 LOC105378494, AFAP1L2
    nsv4977044copy number variation1nstd200human GRCh38 chr10: 114,312,130-114,312,193 , GRCh37.p13 chr10: 116,071,889-116,071,952 AFAP1L2
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