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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5955838copy number variation1nstd209human GRCh38 chr20: 25,923,975-30,219,168 , GRCh37.p13 chr20: 25,904,611-29,453,844 CDC27P3, LOC105379477, 30 more genes
    nsv5668445insertion1nstd207human GRCh38 chr20: 26,073,715-26,073,715 , GRCh37.p13 chr20: 26,054,351-26,054,351 FAM182A
    nsv5666910insertion1nstd207human GRCh38 chr20: 26,074,108-26,074,108 , GRCh37.p13 chr20: 26,054,744-26,054,744 FAM182A
    nsv5598555copy number variation1nstd207human GRCh38 chr20: 26,080,688-26,081,008 , GRCh37.p13 chr20: 26,061,324-26,061,644 FAM182A
    nsv5593402copy number variation1nstd207human GRCh38 chr20: 26,086,266-26,088,694 , GRCh37.p13 chr20: 26,066,902-26,069,330 FAM182A
    nsv5591304copy number variation1nstd207human GRCh38 chr20: 26,080,180-26,080,480 , GRCh37.p13 chr20: 26,060,816-26,061,116 FAM182A
    nsv5590879copy number variation1nstd207human GRCh38 chr20: 26,084,269-26,085,432 , GRCh37.p13 chr20: 26,064,905-26,066,068 FAM182A
    nsv5299884copy number variation1nstd204human GRCh38.p13 chr20: 26,078,601-26,079,300 , GRCh37.p13 chr20: 26,059,237-26,059,936 FAM182A
    nsv5299257copy number variation1nstd204human GRCh38.p13 chr20: 26,077,601-26,087,000 , GRCh37.p13 chr20: 26,058,237-26,067,636 FAM182A
    nsv5298275copy number variation1nstd204human GRCh38.p13 chr20: 26,077,701-26,080,700 , GRCh37.p13 chr20: 26,058,337-26,061,336 FAM182A
    nsv5296349copy number variation1nstd204human GRCh38.p13 chr20: 26,050,201-26,053,500 , GRCh37.p13 chr20: 26,030,837-26,034,136 FAM182A
    nsv5295429copy number variation1nstd204human GRCh38.p13 chr20: 26,064,901-26,068,700 , GRCh37.p13 chr20: 26,045,537-26,049,336 FAM182A
    nsv5293865copy number variation1nstd204human GRCh38.p13 chr20: 26,081,601-26,082,200 , GRCh37.p13 chr20: 26,062,237-26,062,836 FAM182A
    nsv5292724copy number variation1nstd204human GRCh38.p13 chr20: 26,052,001-26,054,000 , GRCh37.p13 chr20: 26,032,637-26,034,636 FAM182A
    nsv5291268copy number variation1nstd204human GRCh38.p13 chr20: 26,082,648-26,084,422 , GRCh37.p13 chr20: 26,063,284-26,065,058 FAM182A
    nsv5290920copy number variation1nstd204human GRCh38.p13 chr20: 26,080,001-26,081,100 , GRCh37.p13 chr20: 26,060,637-26,061,736 FAM182A
    nsv5288322copy number variation1nstd204human GRCh38.p13 chr20: 26,076,101-26,076,800 , GRCh37.p13 chr20: 26,056,737-26,057,436 FAM182A
    nsv5288093copy number variation1nstd204human GRCh38.p13 chr20: 26,077,501-26,078,400 , GRCh37.p13 chr20: 26,058,137-26,059,036 FAM182A
    nsv5286907copy number variation1nstd204human GRCh38.p13 chr20: 26,071,501-26,072,600 , GRCh37.p13 chr20: 26,052,137-26,053,236 BSNDP3, FAM182A
    nsv5286464copy number variation1nstd204human GRCh38.p13 chr20: 26,080,077-26,082,379 , GRCh37.p13 chr20: 26,060,713-26,063,015 FAM182A
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