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Items: 1 to 20 of 449

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5890667copy number variation1nstd209human GRCh38 chr4: 176,261,835-176,261,900 , GRCh37.p13 chr4: 177,182,986-177,183,051 ASB5
    nsv5722752mobile element insertion2nstd211human GRCh38 chr4: 176,242,152-176,242,152 , GRCh37.p13 chr4: 177,163,303-177,163,303 ASB5
    nsv5640160insertion1nstd207human GRCh38 chr4: 176,251,280-176,251,280 , GRCh37.p13 chr4: 177,172,431-177,172,431 ASB5
    nsv5639113insertion1nstd207human GRCh38 chr4: 176,219,120-176,219,120 , GRCh37.p13 chr4: 177,140,271-177,140,271 ASB5
    nsv5636086insertion1nstd207human GRCh38 chr4: 176,218,607-176,218,607 , GRCh37.p13 chr4: 177,139,758-177,139,758 ASB5
    nsv5633973insertion1nstd207human GRCh38 chr4: 176,219,185-176,219,185 , GRCh37.p13 chr4: 177,140,336-177,140,336 ASB5
    nsv5632071insertion1nstd207human GRCh38 chr4: 176,219,101-176,219,101 , GRCh37.p13 chr4: 177,140,252-177,140,252 ASB5
    nsv5630871insertion1nstd207human GRCh38 chr4: 176,219,312-176,219,312 , GRCh37.p13 chr4: 177,140,463-177,140,463 ASB5
    nsv5630803insertion2nstd207human GRCh38 chr4: 176,218,255-176,218,255 , GRCh37.p13 chr4: 177,139,406-177,139,406 ASB5
    nsv5630510insertion1nstd207human GRCh38 chr4: 176,218,347-176,218,347 , GRCh37.p13 chr4: 177,139,498-177,139,498 ASB5
    nsv5629177insertion1nstd207human GRCh38 chr4: 176,218,955-176,218,955 , GRCh37.p13 chr4: 177,140,106-177,140,106 ASB5
    nsv5628817insertion1nstd207human GRCh38 chr4: 176,219,419-176,219,419 , GRCh37.p13 chr4: 177,140,570-177,140,570 ASB5
    nsv5582349copy number variation1nstd207human GRCh38 chr4: 176,218,280-176,218,390 , GRCh37.p13 chr4: 177,139,431-177,139,541 ASB5
    nsv5576245copy number variation1nstd207human GRCh38 chr4: 176,219,079-176,219,130 , GRCh37.p13 chr4: 177,140,230-177,140,281 ASB5
    nsv5574412copy number variation1nstd207human GRCh38 chr4: 176,218,817-176,218,908 , GRCh37.p13 chr4: 177,139,968-177,140,059 ASB5
    nsv5573291copy number variation1nstd207human GRCh38 chr4: 176,219,262-176,219,386 , GRCh37.p13 chr4: 177,140,413-177,140,537 ASB5
    nsv5572405copy number variation1nstd207human GRCh38 chr4: 176,218,533-176,218,791 , GRCh37.p13 chr4: 177,139,684-177,139,942 ASB5
    nsv5567545copy number variation1nstd207human GRCh38 chr4: 176,219,367-176,219,420 , GRCh37.p13 chr4: 177,140,518-177,140,571 ASB5
    nsv5566985copy number variation1nstd207human GRCh38 chr4: 176,218,544-176,218,606 , GRCh37.p13 chr4: 177,139,695-177,139,757 ASB5
    nsv5566252copy number variation1nstd207human GRCh38 chr4: 176,218,151-176,218,225 , GRCh37.p13 chr4: 177,139,302-177,139,376 ASB5
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