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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5728441mobile element insertion1nstd211human GRCh38 chr11: 77,036,723-77,036,723 , GRCh37.p13 chr11|NW_003871081.1: 38,360-38,360 , GRCh37.p13 chr11: 76,747,767-76,747,767 B3GNT6
    nsv5562233mobile element insertion1nstd206human GRCh38 chr11: 77,036,723-77,036,774 , GRCh37.p13 chr11|NW_003871081.1: 38,360-38,411 , GRCh37.p13 chr11: 76,747,767-76,747,818 B3GNT6
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4987403copy number variation1nstd200human GRCh38 chr11: 77,041,800-77,045,082 , GRCh37.p13 chr11: 76,752,847-76,756,129 , GRCh37.p13 chr11|NW_003871081.1: 43,437-46,719 B3GNT6
    nsv4985155copy number variation1nstd200human GRCh38 chr11: 77,040,137-77,046,776 , GRCh37.p13 chr11: 76,751,181-76,757,823 , GRCh37.p13 chr11|NW_003871081.1: 41,774-48,413 B3GNT6, LOC105369399
    nsv4985154copy number variation1nstd200human GRCh38 chr11: 77,032,665-77,032,831 , GRCh37.p13 chr11|NW_003871081.1: 34,302-34,468 , GRCh37.p13 chr11: 76,743,709-76,743,875 B3GNT6
    nsv4839299copy number variation1nstd200human GRCh37 chr11: 76,743,709-76,743,875 , GRCh38.p12 chr11: 77,032,665-77,032,831 B3GNT6
    nsv4832989copy number variation1nstd200human GRCh37 chr11: 76,751,181-76,757,823 , GRCh38.p12 chr11: 77,040,137-77,046,776 LOC105369399, B3GNT6
    nsv4201116copy number variation1nstd166human GRCh37.p13 chr11: 76,731,715-76,825,853 , GRCh38.p12 chr11: 77,020,671-77,114,807 CAPN5, OMP, 4 more genes
    nsv4200290copy number variation1nstd166human GRCh37.p13 chr11: 76,746,983-76,747,094 , GRCh38.p12 chr11: 77,035,939-77,036,050 B3GNT6
    nsv3921121copy number variation1nstd102humanPathogenic GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688 LOC105369441, RNU6-1135P, 296 more genes
    nsv3916301copy number variation1nstd102humanPathogenic GRCh38 chr11: 71,928,796-77,064,521 , GRCh37 chr11: 71,639,842-76,751,808 , NCBI36 chr11: 71,317,490-76,453,216 RN7SL786P, LIPT2-AS1, 146 more genes
    nsv3915804copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895 TPBGL, MAP6, 173 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3898361copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202 SESN3, LOC107984352, 694 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3149861copy number variation1nstd151human GRCh37 chr11: 76,637,598-77,475,739 , GRCh38.p12 chr11: 76,926,554-77,764,694 B3GNT6, AQP11, 15 more genes
    nsv3142968copy number variation1nstd151human GRCh37 chr11: 74,676,806-76,893,648 , GRCh38.p12 chr11: 74,965,761-77,182,603 , LOC107984358, 56 more genes
    nsv2732449copy number variation1nstd130human NCBI36 chr11: 73,243,988-90,057,911 , GRCh37.p13 chr11: 73,566,340-90,418,263 , GRCh38.p12 chr11: 73,855,295-90,685,095 , FOLH1B, 271 more genes
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