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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5533556copy number variation1nstd206human GRCh38 chr16: 63,251,015-63,364,071 , GRCh37.p13 chr16: 63,284,919-63,397,975 LOC105371308, RPS15AP34
    nsv5267900copy number variation1nstd204human GRCh38.p13 chr16: 63,351,201-63,355,300 , GRCh37.p13 chr16: 63,385,105-63,389,204 RPS15AP34, LOC105371308
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv4992949copy number variation1nstd200human GRCh38 chr16: 63,273,444-63,624,757 , GRCh37.p13 chr16: 63,307,348-63,658,661 RPS15AP34, LOC105371308
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4680766copy number variation1nstd189human GRCh38.p12 chr16: 61,813,558-63,362,925 , GRCh37.p13 chr16: 61,847,462-63,396,829 CDH8, RPS15AP34, 6 more genes
    nsv4456077copy number variation1nstd102humanUncertain significance GRCh37 chr16: 53,455,650-64,006,604 , GRCh38.p12 chr16: 53,421,738-63,972,700 MT1DP, RPL23AP91, 167 more genes
    nsv4436581complex substitution1nstd102humanUncertain significance GRCh38.p12 chr16: 56,334,777-90,074,947 , GRCh37 chr16: 56,368,689-90,141,355 AARS1, AP1G1, 662 more genes
    nsv4418292copy number variation1nstd174human GRCh37 chr16: 63,284,038-63,401,297 , GRCh38.p12 chr16: 63,250,134-63,367,393 RPS15AP34, LOC105371308
    nsv4332560sequence alteration1nstd166human GRCh37.p13 chr16: 57,901,049-75,540,778 , GRCh38.p12 chr16: 57,867,145-75,506,880 , AGRP, 331 more genes
    nsv4245264copy number variation1nstd166human GRCh37.p13 chr16: 63,284,908-63,397,941 , GRCh38.p12 chr16: 63,251,004-63,364,037 LOC105371308, RPS15AP34
    nsv3923474copy number variation1nstd102humanUncertain significance NCBI36 chr16: 61,910,485-62,052,192 , GRCh37.p13 chr16: 63,352,984-63,494,691 , GRCh38.p12 chr16: 63,319,080-63,460,787 LOC105371308, RPS15AP34
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 LOC105371237, IGHV3OR16-11, 985 more genes
    nsv3920399copy number variation1nstd102humanPathogenic NCBI36 chr16: 61,517,334-83,176,902 , GRCh37 chr16: 62,959,833-84,619,401 , GRCh38 chr16: 62,925,929-84,585,795 LOC654780, LSM3P5, 385 more genes
    nsv3918521copy number variation1nstd102humanPathogenic NCBI36 chr16: 48,276,933-66,993,116 , GRCh37 chr16: 49,719,432-68,435,615 , GRCh38 chr16: 49,685,521-68,401,712 CYLD-AS2, MT1F, 342 more genes
    nsv3918393copy number variation1nstd102humanUncertain significance NCBI36 chr16: 61,878,482-62,024,709 , GRCh37.p13 chr16: 63,320,981-63,467,208 , GRCh38.p12 chr16: 63,287,077-63,433,304 RPS15AP34, LOC105371308
    nsv3917427copy number variation1nstd102humanBenign NCBI36 chr16: 32,529,496-88,822,254 , GRCh37.p13 chr16: 32,621,995-90,294,753 , GRCh38.p12 chr16: 32,610,674-90,228,345 TXNL4B, KLHL36, 968 more genes
    nsv3916905copy number variation1nstd102humanBenign NCBI36 chr16: 32,481,314-88,822,254 , GRCh37.p13 chr16: 32,573,813-90,294,753 , GRCh38.p12 chr16: 32,562,492-90,228,345 CDH16, TP53TG3HP, 968 more genes
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