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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097024copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,266,142-138,861,289 , GRCh38.p12 chr5: 138,930,453-139,481,704 SLC23A1, RNU5B-4P, 20 more genes
    nsv7097022copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-138,861,289 , GRCh38.p12 chr5: 137,622,098-139,481,704 CDC25C, SLC23A1, 55 more genes
    nsv7096751copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-140,078,137 , GRCh38.p12 chr5: 137,622,098-140,698,552 CDC25C, LOC100128966, 94 more genes
    nsv7057082inversion1nstd229human GRCh38 chr5: 139,208,712-142,493,851 , GRCh37.p13 chr5: 138,544,401-141,873,416 SPRY4-AS1, SPRY4, 151 more genes
    nsv6794064copy number variation1nstd229human GRCh38 chr5: 139,260,658-139,274,282 , GRCh37.p13 chr5: 138,596,347-138,609,971 SNORA74D, MATR3, 1 more genes
    nsv6780567copy number variation1nstd229human GRCh38 chr5: 139,264,264-139,309,626 , GRCh37.p13 chr5: 138,599,953-138,645,315 MATR3, SNHG4, 3 more genes
    nsv6780059copy number variation1nstd229human GRCh38 chr5: 139,280,225-139,291,083 , GRCh37.p13 chr5: 138,615,914-138,626,772 SNHG4, MATR3
    nsv6778440copy number variation1nstd229human GRCh38 chr5: 139,104,141-139,300,722 , GRCh37.p13 chr5: 138,439,830-138,636,411 SNHG4, SNORA74A, 5 more genes
    nsv6636861copy number variation1nstd102humanUncertain significance GRCh37 chr5: 137,893,096-138,868,605 , GRCh38.p12 chr5: 138,557,407-139,489,020 HSPA9, ECSCR, 27 more genes
    nsv6405600copy number variation1nstd223human GRCh38 chr5: 137,606,101-142,582,700 , GRCh37.p13 chr5: 136,941,790-141,962,265 TMCO6, PCDHB17P, 191 more genes
    nsv6311751copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,608,441-138,668,366 , GRCh38.p12 chr5: 139,272,752-139,332,677 MATR3, SNORA74A, 4 more genes
    nsv6291250copy number variation1nstd102humanUncertain significance GRCh37 chr5: 138,386,858-138,935,115 , GRCh38.p12 chr5: 139,051,169-139,555,530 STING1, SPATA24, 18 more genes
    nsv6135653copy number variation1nstd213human GRCh37 chr5: 138,340,000-143,460,001 , GRCh38.p12 chr5: 139,004,311-144,080,436 CD14, DIAPH1, 170 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6135116copy number variation1nstd213human GRCh37 chr5: 138,320,000-138,890,001 , GRCh38.p12 chr5: 138,984,311-139,510,416 MATR3, SLC23A1, 20 more genes
    nsv5455624copy number variation1nstd206human GRCh38 chr5: 139,275,347-139,275,931 , GRCh37.p13 chr5: 138,611,036-138,611,620 SNHG4, SNORA74D, 1 more genes
    nsv5381510copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,633,338-140,998,481 , GRCh38.p12 chr5: 137,297,649-141,618,914 RNA5SP195, LOC112267855, 174 more genes
    nsv5300443copy number variation1nstd204human GRCh37.p13 chr5: 138,611,034-138,611,629 , GRCh38.p13 chr5: 139,275,345-139,275,940 MATR3, SNHG4, 1 more genes
    nsv5086243mobile element insertion1nstd203human GRCh38 chr5: 139,279,907-139,279,926 , GRCh37.p13 chr5: 138,615,596-138,615,615 SNHG4, MATR3
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
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