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Items: 1 to 20 of 293

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905674copy number variation1nstd209human GRCh38 chr6: 35,950,396-35,950,528 , GRCh37.p13 chr6: 35,918,173-35,918,305 SLC26A8
    nsv5900522copy number variation1nstd209human GRCh38 chr6: 36,021,946-36,022,243 , GRCh37.p13 chr6: 35,989,723-35,990,020 SLC26A8
    nsv5892330copy number variation1nstd209human GRCh38 chr6: 35,948,470-36,584,214 , GRCh37.p13 chr6: 35,916,247-36,551,991 SLC26A8, STK38, 17 more genes
    nsv5690712mobile element insertion2nstd211human GRCh38 chr6: 35,959,401-35,959,401 , GRCh37.p13 chr6: 35,927,178-35,927,178 SLC26A8
    nsv5689394mobile element insertion2nstd211human GRCh38 chr6: 36,003,130-36,003,130 , GRCh37.p13 chr6: 35,970,907-35,970,907 SLC26A8, LOC105375034
    nsv5637883insertion1nstd207human GRCh38 chr6: 35,959,391-35,959,391 , GRCh37.p13 chr6: 35,927,168-35,927,168 SLC26A8
    nsv5583425copy number variation1nstd207human GRCh38 chr6: 35,950,396-35,950,528 , GRCh37.p13 chr6: 35,918,173-35,918,305 SLC26A8
    nsv5471909copy number variation1nstd206human GRCh38 chr6: 35,988,722-35,988,912 , GRCh37.p13 chr6: 35,956,499-35,956,689 SLC26A8, DPRXP2, 1 more genes
    nsv5470084copy number variation1nstd206human GRCh38 chr6: 35,950,414-35,950,529 , GRCh37.p13 chr6: 35,918,191-35,918,306 SLC26A8
    nsv5455005copy number variation1nstd206human GRCh38 chr6: 35,994,320-36,001,385 , GRCh37.p13 chr6: 35,962,097-35,969,162 LOC105375034, SLC26A8
    nsv5408097mobile element insertion1nstd206human GRCh38 chr6: 36,003,130-36,003,181 , GRCh37.p13 chr6: 35,970,907-35,970,958 SLC26A8, LOC105375034
    nsv5395456mobile element insertion1nstd206human GRCh38 chr6: 35,959,401-35,959,409 , GRCh37.p13 chr6: 35,927,178-35,927,186 SLC26A8
    nsv5362855translocation1nstd200human GRCh38 chr6: 36,010,431-36,010,431 , GRCh38 chr6: 36,010,993-36,010,993 , GRCh37.p13 chr6: 35,978,208-35,978,208 , GRCh37.p13 chr6: 35,978,770-35,978,770 LOC105375034, SLC26A8
    nsv5362854translocation1nstd200human GRCh38 chr6: 35,979,856-35,979,856 , GRCh38 chr6: 35,979,933-35,979,933 , GRCh37.p13 chr6: 35,947,710-35,947,710 , GRCh37.p13 chr6: 35,947,633-35,947,633 LOC105375035, SLC26A8
    nsv5228661copy number variation1nstd204human GRCh38.p13 chr6: 35,950,408-35,951,566 , GRCh37.p13 chr6: 35,918,185-35,919,343 SLC26A8
    nsv5200371copy number variation1nstd102humanPathogenic GRCh37 chr6: 34,401,304-38,435,497 , GRCh38.p12 chr6: 34,433,527-38,467,721 RPS15AP19, FKBP5, 95 more genes
    nsv5116793mobile element insertion1nstd203human GRCh38 chr6: 35,959,391-35,959,401 , GRCh37.p13 chr6: 35,927,168-35,927,178 SLC26A8
    nsv5116750mobile element insertion1nstd203human GRCh38 chr6: 35,991,227-35,991,241 , GRCh37.p13 chr6: 35,959,004-35,959,018 SLC26A8, LOC105375035
    nsv5107906mobile element insertion1nstd203human GRCh38 chr6: 35,959,393-35,959,401 , GRCh37.p13 chr6: 35,927,170-35,927,178 SLC26A8
    nsv5104458mobile element insertion1nstd203human GRCh38 chr6: 35,959,394-35,959,401 , GRCh37.p13 chr6: 35,927,171-35,927,178 SLC26A8
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