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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5951107insertion1nstd209human GRCh38 chr6: 11,133,754-11,133,754 , GRCh37.p13 chr6: 11,133,987-11,133,987 SMIM13
    nsv5904734copy number variation1nstd209human GRCh38 chr6: 11,117,314-11,117,487 , GRCh37.p13 chr6: 11,117,547-11,117,720 SMIM13
    nsv5843652copy number variation1nstd209human GRCh38 chr6: 11,128,264-11,129,363 , GRCh37.p13 chr6: 11,128,497-11,129,596 SMIM13
    nsv5843651copy number variation1nstd209human GRCh38 chr6: 11,126,564-11,128,063 , GRCh37.p13 chr6: 11,126,797-11,128,296 SMIM13
    nsv5685341mobile element insertion2nstd211human GRCh38 chr6: 11,133,769-11,133,769 , GRCh37.p13 chr6: 11,134,002-11,134,002 SMIM13
    nsv5627536insertion1nstd207human GRCh38 chr6: 11,117,339-11,117,339 , GRCh37.p13 chr6: 11,117,572-11,117,572 SMIM13
    nsv5469741copy number variation1nstd206human GRCh38 chr6: 11,117,321-11,117,488 , GRCh37.p13 chr6: 11,117,554-11,117,721 SMIM13
    nsv5465311copy number variation1nstd206human GRCh38 chr6: 11,124,503-11,124,909 , GRCh37.p13 chr6: 11,124,736-11,125,142 SMIM13
    nsv5401252mobile element insertion1nstd206human GRCh38 chr6: 11,133,769-11,133,820 , GRCh37.p13 chr6: 11,134,002-11,134,053 SMIM13
    nsv5378197translocation1nstd200human GRCh38 chr6: 11,124,909-11,124,909 , GRCh38 chr6: 11,124,503-11,124,503 , GRCh37.p13 chr6: 11,124,736-11,124,736 , GRCh37.p13 chr6: 11,125,142-11,125,142 SMIM13
    nsv5099096mobile element insertion1nstd203human GRCh38 chr6: 11,117,009-11,117,009 , GRCh37.p13 chr6: 11,117,242-11,117,242 SMIM13
    nsv5098201mobile element insertion1nstd203human GRCh38 chr6: 11,133,754-11,133,769 , GRCh37.p13 chr6: 11,133,987-11,134,002 SMIM13
    nsv5095964mobile element insertion1nstd203human GRCh38 chr6: 11,116,978-11,117,009 , GRCh37.p13 chr6: 11,117,211-11,117,242 SMIM13
    nsv5091048mobile element insertion1nstd203human GRCh38 chr6: 11,117,138-11,117,181 , GRCh37.p13 chr6: 11,117,371-11,117,414 SMIM13
    nsv5090829mobile element insertion1nstd203human GRCh38 chr6: 11,133,761-11,133,769 , GRCh37.p13 chr6: 11,133,994-11,134,002 SMIM13
    nsv5087797mobile element insertion1nstd203human GRCh38 chr6: 11,103,695-11,103,712 , GRCh37.p13 chr6: 11,103,928-11,103,945 ERVFRD-1, SMIM13
    nsv5084935mobile element insertion1nstd203human GRCh38 chr6: 11,124,554-11,124,569 , GRCh37.p13 chr6: 11,124,787-11,124,802 SMIM13
    nsv5084748mobile element insertion1nstd203human GRCh38 chr6: 11,116,982-11,117,009 , GRCh37.p13 chr6: 11,117,215-11,117,242 SMIM13
    nsv4934419copy number variation1nstd200human GRCh38 chr6: 11,117,314-11,117,488 , GRCh37.p13 chr6: 11,117,547-11,117,721 SMIM13
    nsv4934387copy number variation1nstd200human GRCh38 chr6: 7,366,072-12,459,747 , GRCh37.p13 chr6: 7,366,305-12,459,979 , DSP, 90 more genes
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