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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5890113copy number variation1nstd209human GRCh38 chr6: 160,450,582-160,450,680 , GRCh37.p13 chr6: 160,871,614-160,871,712 SLC22A3
    nsv5635517insertion1nstd207human GRCh38 chr6: 160,372,644-160,372,644 , GRCh37.p13 chr6: 160,793,676-160,793,676 SLC22A3
    nsv5556636sequence alteration1nstd206human GRCh38 chr6: 160,372,606-160,372,647 , GRCh37.p13 chr6: 160,793,638-160,793,679 SLC22A3
    nsv5461151copy number variation1nstd206human GRCh38 chr6: 159,927,300-160,654,790 , GRCh37.p13 chr6: 160,348,332-161,075,822 SLC22A2, CHP1P2, 8 more genes
    nsv5459470copy number variation1nstd206human GRCh38 chr6: 160,425,034-160,425,107 , GRCh37.p13 chr6: 160,846,066-160,846,139 SLC22A3
    nsv5456562copy number variation1nstd206human GRCh38 chr6: 160,402,506-160,402,655 , GRCh37.p13 chr6: 160,823,538-160,823,687 SLC22A3
    nsv5369993translocation1nstd200human GRCh38 chr6: 160,425,107-160,425,107 , GRCh38 chr6: 160,425,034-160,425,034 , GRCh37.p13 chr6: 160,846,139-160,846,139 , GRCh37.p13 chr6: 160,846,066-160,846,066 SLC22A3
    nsv5336164translocation1nstd200human GRCh37 chr6: 160,846,139-160,846,139 , GRCh37 chr6: 160,846,066-160,846,066 , GRCh38.p12 chr6: 160,425,107-160,425,107 , GRCh38.p12 chr6: 160,425,034-160,425,034 SLC22A3
    nsv5238301copy number variation1nstd204human GRCh38.p13 chr6: 160,400,001-160,404,300 , GRCh37.p13 chr6: 160,821,033-160,825,332 SLC22A3
    nsv4945897copy number variation1nstd200human GRCh38 chr6: 160,328,970-160,362,094 , GRCh37.p13 chr6: 160,750,002-160,783,126 SLC22A3
    nsv4945895copy number variation1nstd200human GRCh38 chr6: 160,281,909-160,375,764 , GRCh37.p13 chr6: 160,702,941-160,796,796 SLC22A3
    nsv4943728copy number variation1nstd200human GRCh38 chr6: 160,444,797-160,445,358 , GRCh37.p13 chr6: 160,865,829-160,866,390 SLC22A3
    nsv4943727copy number variation1nstd200human GRCh38 chr6: 160,398,008-160,399,449 , GRCh37.p13 chr6: 160,819,040-160,820,481 SLC22A3
    nsv4943726copy number variation1nstd200human GRCh38 chr6: 160,377,471-160,384,289 , GRCh37.p13 chr6: 160,798,503-160,805,321 SLC22A3
    nsv4943725copy number variation1nstd200human GRCh38 chr6: 160,369,590-160,379,388 , GRCh37.p13 chr6: 160,790,622-160,800,420 SLC22A3
    nsv4824842copy number variation1nstd200human GRCh37 chr6: 160,750,002-160,783,126 , GRCh38.p12 chr6: 160,328,970-160,362,094 SLC22A3
    nsv4766814inversion1nstd199human GRCh37 chr6: 153,752,140-161,206,728 , GRCh38.p12 chr6: 153,431,005-160,785,696 , ACAT2, 111 more genes
    nsv4679732copy number variation1nstd189human GRCh38.p12 chr6: 160,227,236-160,509,796 , GRCh37.p13 chr6: 160,648,268-160,930,828 SLC22A3, SLC22A2, 2 more genes
    nsv4563612mobile element insertion1nstd166human GRCh37.p13 chr6: 160,840,980-160,840,980 , GRCh38.p12 chr6: 160,419,948-160,419,948 SLC22A3
    nsv4548068insertion1nstd166human GRCh37.p13 chr6: 160,793,638-160,793,638 , GRCh38.p12 chr6: 160,372,606-160,372,606 SLC22A3
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