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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098182copy number variation1nstd102humanUncertain significance GRCh37 chr8: 70,591,593-70,594,598 , GRCh38.p12 chr8: 69,679,358-69,682,363 SLCO5A1
    nsv7061399inversion1nstd229human GRCh38 chr8: 69,772,835-69,772,889 , GRCh37.p13 chr8: 70,685,070-70,685,124 SLCO5A1
    nsv7059419inversion1nstd229human GRCh38 chr8: 69,398,206-69,710,607 , GRCh37.p13 chr8: 70,310,441-70,622,842 SLCO5A1, LINC01603, 3 more genes
    nsv6856315copy number variation1nstd229human GRCh38 chr8: 69,716,010-70,222,698 , GRCh37.p13 chr8: 70,628,245-71,134,933 RN7SL675P, RNA5SP270, 10 more genes
    nsv6853764copy number variation1nstd229human GRCh38 chr8: 69,781,775-69,808,414 , GRCh37.p13 chr8: 70,694,010-70,720,649 SLCO5A1, TMX1P2
    nsv6853591copy number variation1nstd229human GRCh38 chr8: 69,719,197-69,719,503 , GRCh37.p13 chr8: 70,631,432-70,631,738 LOC105375889, SLCO5A1
    nsv6851706copy number variation1nstd229human GRCh38 chr8: 69,769,512-69,774,433 , GRCh37.p13 chr8: 70,681,747-70,686,668 SLCO5A1
    nsv6851064copy number variation1nstd229human GRCh38 chr8: 69,774,055-69,775,707 , GRCh37.p13 chr8: 70,686,290-70,687,942 SLCO5A1
    nsv6850287copy number variation1nstd229human GRCh38 chr8: 69,677,693-69,698,825 , GRCh37.p13 chr8: 70,589,928-70,611,060 RN7SKP29, SLCO5A1
    nsv6849223copy number variation1nstd229human GRCh38 chr8: 69,678,946-69,679,386 , GRCh37.p13 chr8: 70,591,181-70,591,621 SLCO5A1
    nsv6848836copy number variation1nstd229human GRCh38 chr8: 69,705,923-69,708,586 , GRCh37.p13 chr8: 70,618,158-70,620,821 LOC105375889, SLCO5A1
    nsv6848139copy number variation1nstd229human GRCh38 chr8: 69,802,665-70,039,383 , GRCh37.p13 chr8: 70,714,900-70,951,618 SUMO2P20, RNA5SP270, 4 more genes
    nsv6847728copy number variation1nstd229human GRCh38 chr8: 69,122,674-69,698,564 , GRCh37.p13 chr8: 70,034,909-70,610,799 RN7SKP29, SLCO5A1, 4 more genes
    nsv6847361copy number variation1nstd229human GRCh38 chr8: 69,827,508-69,836,817 , GRCh37.p13 chr8: 70,739,743-70,749,052 SLCO5A1
    nsv6847116copy number variation1nstd229human GRCh38 chr8: 68,675,587-70,209,684 , GRCh37.p13 chr8: 69,587,822-71,121,919 LINC01603, SUMO2P20, 20 more genes
    nsv6844008copy number variation1nstd229human GRCh38 chr8: 69,827,664-69,827,985 , GRCh37.p13 chr8: 70,739,899-70,740,220 SLCO5A1
    nsv6843570copy number variation1nstd229human GRCh38 chr8: 69,689,968-69,693,345 , GRCh37.p13 chr8: 70,602,203-70,605,580 SLCO5A1
    nsv6843323copy number variation1nstd229human GRCh38 chr8: 69,642,158-69,712,691 , GRCh37.p13 chr8: 70,554,393-70,624,926 RN7SKP29, SULF1, 2 more genes
    nsv6841515copy number variation1nstd229human GRCh38 chr8: 69,703,121-69,703,232 , GRCh37.p13 chr8: 70,615,356-70,615,467 SLCO5A1
    nsv6841272copy number variation1nstd229human GRCh38 chr8: 69,674,653-69,674,685 , GRCh37.p13 chr8: 70,586,888-70,586,920 SLCO5A1
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