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Items: 1 to 20 of 418

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131277insertion1nstd186human GRCh37 chr12: 96,088,126-96,088,146 , GRCh38.p12 chr12: 95,694,350-95,694,370 NTN4
    nsv6120730copy number variation1nstd186human GRCh37 chr12: 96,143,532-96,143,778 , GRCh38.p12 chr12: 95,749,754-95,750,000 NTN4
    nsv5943019copy number variation1nstd209human GRCh38 chr12: 95,749,747-95,749,999 , GRCh37.p13 chr12: 96,143,525-96,143,777 NTN4
    nsv5939510copy number variation1nstd209human GRCh38 chr12: 95,714,413-95,714,526 , GRCh37.p13 chr12: 96,108,191-96,108,304 NTN4
    nsv5929554copy number variation1nstd209human GRCh38 chr12: 95,627,013-95,700,426 , GRCh37.p13 chr12: 96,020,789-96,094,202 PGAM1P5, NTN4
    nsv5928611copy number variation1nstd209human GRCh38 chr12: 95,761,313-95,761,367 , GRCh37.p13 chr12: 96,155,091-96,155,145 NTN4
    nsv5865561copy number variation1nstd209human GRCh38 chr12: 95,669,733-95,676,920 , GRCh37.p13 chr12: 96,063,509-96,070,696 NTN4, PGAM1P5
    nsv5861974copy number variation1nstd209human GRCh38 chr12: 95,672,329-95,674,928 , GRCh37.p13 chr12: 96,066,105-96,068,704 NTN4, PGAM1P5
    nsv5854961copy number variation1nstd209human GRCh38 chr12: 95,673,729-95,684,320 , GRCh37.p13 chr12: 96,067,505-96,078,096 NTN4, PGAM1P5
    nsv5853349copy number variation1nstd209human GRCh38 chr12: 95,658,750-95,662,581 , GRCh37.p13 chr12: 96,052,526-96,056,357 PGAM1P5, NTN4
    nsv5850869copy number variation1nstd209human GRCh38 chr12: 95,657,750-95,666,188 , GRCh37.p13 chr12: 96,051,526-96,059,964 NTN4, PGAM1P5
    nsv5731038mobile element insertion2nstd211human GRCh38 chr12: 95,715,034-95,715,034 , GRCh37.p13 chr12: 96,108,812-96,108,812 NTN4, LOC105369919
    nsv5726589mobile element insertion2nstd211human GRCh38 chr12: 95,743,154-95,743,154 , GRCh37.p13 chr12: 96,136,932-96,136,932 NTN4
    nsv5705922mobile element insertion1nstd211human GRCh38 chr12: 95,665,273-95,665,273 , GRCh37.p13 chr12: 96,059,049-96,059,049 PGAM1P5, NTN4
    nsv5699600mobile element insertion1nstd211human GRCh38 chr12: 95,716,058-95,716,058 , GRCh37.p13 chr12: 96,109,836-96,109,836 NTN4, LOC105369919
    nsv5598934copy number variation1nstd207human GRCh38 chr12: 95,749,747-95,749,999 , GRCh37.p13 chr12: 96,143,525-96,143,777 NTN4
    nsv5597682copy number variation1nstd207human GRCh38 chr12: 95,761,317-95,761,371 , GRCh37.p13 chr12: 96,155,095-96,155,149 NTN4
    nsv5595812copy number variation1nstd207human GRCh38 chr12: 95,749,871-95,749,934 , GRCh37.p13 chr12: 96,143,649-96,143,712 NTN4
    nsv5560418mobile element insertion1nstd206human GRCh38 chr12: 95,715,034-95,715,085 , GRCh37.p13 chr12: 96,108,812-96,108,863 LOC105369919, NTN4
    nsv5560409mobile element insertion1nstd206human GRCh38 chr12: 95,743,154-95,743,205 , GRCh37.p13 chr12: 96,136,932-96,136,983 NTN4
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