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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
    nsv7053326inversion1nstd229human GRCh38 chr1: 183,856,809-187,909,288 , GRCh37.p13 chr1: 183,825,943-187,878,419 RGL1, TPR, 49 more genes
    nsv6645830copy number variation1nstd229human GRCh38 chr1: 185,633,801-185,674,300 , GRCh37.p13 chr1: 185,602,933-185,643,432 GS1-204I12.4, LOC107985239
    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
    nsv6548934inversion1nstd223human GRCh38 chr1: 183,856,809-187,909,292 , GRCh37.p13 chr1: 183,825,943-187,878,423 LOC105371649, LINC01633, 49 more genes
    nsv6325116copy number variation1nstd223human GRCh38 chr1: 185,646,601-185,651,900 , GRCh37.p13 chr1: 185,615,733-185,621,032 LOC107985239, GS1-204I12.4
    nsv6290451copy number variation1nstd102humanPathogenic GRCh37 chr1: 178,522,021-190,322,133 , GRCh38.p12 chr1: 178,552,886-190,353,003 RNU7-13P, LOC105371642, 167 more genes
    nsv6153058copy number variation1nstd214human GRCh38 chr1: 185,655,787-185,655,844 , GRCh37.p13 chr1: 185,624,919-185,624,976 LOC107985239, GS1-204I12.4
    nsv6133952copy number variation1nstd213human GRCh37 chr1: 182,620,000-185,630,001 , GRCh38.p12 chr1: 182,650,865-185,660,869 DHX9, IVNS1ABP, 54 more genes
    nsv6133950copy number variation1nstd213human GRCh37 chr1: 178,070,000-205,920,001 , GRCh38.p12 chr1: 178,100,865-205,950,873 ADORA1, CACNA1E, 442 more genes
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
    nsv6133607copy number variation1nstd213human GRCh37 chr1: 185,330,000-185,870,001 , GRCh38.p12 chr1: 185,360,868-185,900,869 HMCN1, LINC01350, 4 more genes
    nsv6133573copy number variation1nstd213human GRCh37 chr1: 173,820,000-189,960,001 , GRCh38.p12 chr1: 173,850,862-189,990,871 ABL2, ASTN1, 235 more genes
    nsv5982110copy number variation1nstd212human GRCh38 chr1: 185,655,817-185,655,876 , GRCh37.p13 chr1: 185,624,949-185,625,008 LOC107985239, GS1-204I12.4
    nsv5949273insertion1nstd209human GRCh38 chr1: 185,651,639-185,651,639 , GRCh37.p13 chr1: 185,620,771-185,620,771 GS1-204I12.4, LOC107985239
    nsv5885513copy number variation1nstd209human GRCh38 chr1: 185,655,820-185,655,887 , GRCh37.p13 chr1: 185,624,952-185,625,019 GS1-204I12.4, LOC107985239
    nsv5679109mobile element insertion2nstd211human GRCh38 chr1: 185,651,657-185,651,657 , GRCh37.p13 chr1: 185,620,789-185,620,789 LOC107985239, GS1-204I12.4
    nsv5606358insertion1nstd207human GRCh38 chr1: 185,651,639-185,651,639 , GRCh37.p13 chr1: 185,620,771-185,620,771 LOC107985239, GS1-204I12.4
    nsv5578104copy number variation1nstd207human GRCh38 chr1: 185,655,817-185,655,884 , GRCh37.p13 chr1: 185,624,949-185,625,016 LOC107985239, GS1-204I12.4
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