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Items: 1 to 20 of 217

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099254copy number variation1nstd231human GRCh38.p12 chr1: 182,376,401-191,898,122 , GRCh37 chr1: 182,345,536-191,867,252 DHX9, GLUL, 99 more genes
    nsv7095948copy number variation1nstd102humanPathogenic GRCh37 chr1: 183,542,300-183,542,447 , GRCh38.p12 chr1: 183,573,165-183,573,312 NCF2
    nsv7095564copy number variation1nstd102humanUncertain significance GRCh37 chr1: 183,546,714-183,559,464 , GRCh38.p12 chr1: 183,577,579-183,590,329 NCF2, LOC100526839
    nsv7051435inversion1nstd229human GRCh38 chr1: 183,586,444-183,589,928 , GRCh37.p13 chr1: 183,555,579-183,559,063 NCF2, LOC100526839
    nsv6646057copy number variation1nstd229human GRCh38 chr1: 183,574,255-183,579,129 , GRCh37.p13 chr1: 183,543,390-183,548,264 NCF2
    nsv6646056copy number variation1nstd229human GRCh38 chr1: 183,560,274-183,563,193 , GRCh37.p13 chr1: 183,529,409-183,532,328 NCF2
    nsv6645997copy number variation1nstd229human GRCh38 chr1: 183,561,436-183,603,358 , GRCh37.p13 chr1: 183,530,571-183,572,493 LOC100526839, NCF2
    nsv6645550copy number variation1nstd229human GRCh38 chr1: 183,556,231-183,560,095 , GRCh37.p13 chr1: 183,525,366-183,529,230 NCF2
    nsv6637124copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,727,182-192,260,142 , GRCh38.p12 chr1: 179,758,047-192,291,012 LOC101928933, KIAA1614-AS1, 148 more genes
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6553156inversion1nstd223human GRCh38 chr1: 183,558,427-183,559,735 , GRCh37.p13 chr1: 183,527,562-183,528,870 NCF2
    nsv6538365inversion1nstd223human GRCh38 chr1: 178,815,320-184,820,865 , GRCh37.p13 chr1: 178,784,455-184,789,999 NPHS2, COLGALT2, 111 more genes
    nsv6327543copy number variation1nstd223human GRCh38 chr1: 183,575,202-183,585,358 , GRCh37.p13 chr1: 183,544,337-183,554,493 NCF2
    nsv6325052copy number variation1nstd223human GRCh38 chr1: 183,574,255-183,579,124 , GRCh37.p13 chr1: 183,543,390-183,548,259 NCF2
    nsv6324826copy number variation1nstd223human GRCh38 chr1: 183,573,198-183,573,666 , GRCh37.p13 chr1: 183,542,333-183,542,801 NCF2
    nsv6324121copy number variation1nstd223human GRCh38 chr1: 183,559,101-183,560,900 , GRCh37.p13 chr1: 183,528,236-183,530,035 NCF2
    nsv6318567copy number variation1nstd223human GRCh38 chr1: 183,561,436-183,603,355 , GRCh37.p13 chr1: 183,530,571-183,572,490 LOC100526839, NCF2
    nsv6315280copy number variation1nstd102humanUncertain significance GRCh37 chr1: 183,529,409-183,559,740 , GRCh38.p12 chr1: 183,560,274-183,590,605 NCF2, LOC100526839
    nsv6310925copy number variation1nstd102humanPathogenic GRCh37 chr1: 183,543,602-183,543,776 , GRCh38.p12 chr1: 183,574,467-183,574,641 NCF2
    nsv6310922copy number variation1nstd102humanUncertain significance GRCh37 chr1: 179,520,308-183,559,464 , GRCh38.p12 chr1: 179,551,173-183,590,329 NMNAT2, FAM163A, 78 more genes
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