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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
    nsv6646255copy number variation1nstd229human GRCh38 chr1: 185,127,393-185,162,881 , GRCh37.p13 chr1: 185,096,525-185,132,013 SWT1, TRMT1L
    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
    nsv6635249copy number variation1nstd227human GRCh38.p12 chr1: 185,119,193-185,154,498 , GRCh37 chr1: 185,088,325-185,123,630 TRMT1L
    nsv6626058copy number variation4nstd224human GRCh37 chr1: 185,094,084-185,130,019 , GRCh38.p12 chr1: 185,124,952-185,160,887 SWT1, TRMT1L
    nsv6625929copy number variation2nstd224human GRCh37 chr1: 185,113,120-185,130,019 , GRCh38.p12 chr1: 185,143,988-185,160,887 TRMT1L, SWT1
    nsv6625688copy number variation5nstd224human GRCh37 chr1: 185,106,781-185,130,019 , GRCh38.p12 chr1: 185,137,649-185,160,887 SWT1, TRMT1L
    nsv6551655inversion1nstd223human GRCh38 chr1: 185,131,094-185,131,877 , GRCh37.p13 chr1: 185,100,226-185,101,009 TRMT1L
    nsv6548934inversion1nstd223human GRCh38 chr1: 183,856,809-187,909,292 , GRCh37.p13 chr1: 183,825,943-187,878,423 LOC105371649, LINC01633, 49 more genes
    nsv6328997copy number variation1nstd223human GRCh38 chr1: 185,135,258-185,135,682 , GRCh37.p13 chr1: 185,104,390-185,104,814 TRMT1L
    nsv6326728copy number variation1nstd223human GRCh38 chr1: 185,134,740-185,137,290 , GRCh37.p13 chr1: 185,103,872-185,106,422 TRMT1L
    nsv6325719copy number variation1nstd223human GRCh38 chr1: 185,120,301-185,121,200 , GRCh37.p13 chr1: 185,089,433-185,090,332 TRMT1L
    nsv6321179copy number variation1nstd223human GRCh38 chr1: 185,123,101-185,124,200 , GRCh37.p13 chr1: 185,092,233-185,093,332 TRMT1L
    nsv6318223copy number variation1nstd223human GRCh38 chr1: 185,127,393-185,162,881 , GRCh37.p13 chr1: 185,096,525-185,132,013 SWT1, TRMT1L
    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
    nsv6290164copy number variation1nstd102humanUncertain significance GRCh37 chr1: 185,109,784-185,132,629 , GRCh38.p12 chr1: 185,140,652-185,163,497 TRMT1L, SWT1
    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
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