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Items: 1 to 20 of 632

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112729copy number variation1nstd102humannot provided GRCh37 chr5: 116,419,511-120,022,321 , GRCh38.p12 chr5: 117,083,815-120,686,626 RN7SL174P, LINC02148, 35 more genes
    nsv5965153insertion1nstd209human GRCh38 chr5: 117,541,669-117,541,669 , GRCh37.p13 chr5: 116,877,364-116,877,364 LINC00992
    nsv5963099insertion1nstd209human GRCh38 chr5: 117,561,442-117,561,442 , GRCh37.p13 chr5: 116,897,137-116,897,137 LINC00992
    nsv5962190insertion1nstd209human GRCh38 chr5: 117,422,873-117,422,873 , GRCh37.p13 chr5: 116,758,569-116,758,569 LINC00992
    nsv5958872insertion1nstd209human GRCh38 chr5: 117,427,390-117,427,390 , GRCh37.p13 chr5: 116,763,086-116,763,086 LINC00992
    nsv5906323copy number variation1nstd209human GRCh38 chr5: 117,509,808-117,521,389 , GRCh37.p13 chr5: 116,845,503-116,857,084 LINC00992
    nsv5899933copy number variation1nstd209human GRCh38 chr5: 117,500,374-117,500,679 , GRCh37.p13 chr5: 116,836,069-116,836,374 LINC00992
    nsv5895001copy number variation1nstd209human GRCh38 chr5: 117,420,340-117,420,905 , GRCh37.p13 chr5: 116,756,036-116,756,601 LINC00992
    nsv5893434copy number variation1nstd209human GRCh38 chr5: 117,449,922-117,452,798 , GRCh37.p13 chr5: 116,785,618-116,788,494 LINC00992
    nsv5841346copy number variation1nstd209human GRCh38 chr5: 117,487,136-117,488,235 , GRCh37.p13 chr5: 116,822,831-116,823,930 LINC00992
    nsv5841345copy number variation1nstd209human GRCh38 chr5: 117,475,493-117,476,692 , GRCh37.p13 chr5: 116,811,188-116,812,387 LINC00992
    nsv5841344copy number variation1nstd209human GRCh38 chr5: 117,449,865-117,452,884 , GRCh37.p13 chr5: 116,785,561-116,788,580 LINC00992
    nsv5841343copy number variation1nstd209human GRCh38 chr5: 117,439,248-117,440,347 , GRCh37.p13 chr5: 116,774,944-116,776,043 LINC00992
    nsv5840711copy number variation1nstd209human GRCh38 chr5: 117,539,356-117,541,429 , GRCh37.p13 chr5: 116,875,051-116,877,124 LINC00992
    nsv5840710copy number variation1nstd209human GRCh38 chr5: 117,510,400-117,513,580 , GRCh37.p13 chr5: 116,846,095-116,849,275 LINC00992
    nsv5840709copy number variation1nstd209human GRCh38 chr5: 117,509,950-117,521,380 , GRCh37.p13 chr5: 116,845,645-116,857,075 LINC00992
    nsv5683820mobile element insertion2nstd211human GRCh38 chr5: 117,561,456-117,561,456 , GRCh37.p13 chr5: 116,897,151-116,897,151 LINC00992
    nsv5679268mobile element insertion2nstd211human GRCh38 chr5: 117,427,402-117,427,402 , GRCh37.p13 chr5: 116,763,098-116,763,098 LINC00992
    nsv5678914mobile element insertion2nstd211human GRCh38 chr5: 117,534,409-117,534,409 , GRCh37.p13 chr5: 116,870,104-116,870,104 LINC00992
    nsv5643901insertion1nstd207human GRCh38 chr5: 117,542,447-117,542,447 , GRCh37.p13 chr5: 116,878,142-116,878,142 LINC00992
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