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Items: 1 to 20 of 186

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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
    nsv6646031copy number variation1nstd229human GRCh38 chr1: 182,585,301-182,596,100 , GRCh37.p13 chr1: 182,554,436-182,565,235 RNASEL
    nsv6645894copy number variation1nstd229human GRCh38 chr1: 182,573,676-182,587,669 , GRCh37.p13 chr1: 182,542,811-182,556,804 RNASEL
    nsv6645519copy number variation1nstd229human GRCh38 chr1: 182,589,291-182,599,857 , GRCh37.p13 chr1: 182,558,426-182,568,992 RGS16, RNASEL
    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
    nsv6636857copy number variation1nstd102humanUncertain significance GRCh37 chr1: 182,442,865-182,609,349 , GRCh38.p12 chr1: 182,473,730-182,640,214 RGSL1, RGS16, 3 more genes
    nsv6636465copy number variation1nstd102humanUncertain significance GRCh37 chr1: 182,443,031-182,609,230 , GRCh38.p12 chr1: 182,473,896-182,640,095 LINC01686, RGSL1, 3 more genes
    nsv6625927copy number variation1nstd224human GRCh37 chr1: 182,449,249-182,611,109 , GRCh38.p12 chr1: 182,480,114-182,641,974 RNASEL, RGS16, 3 more genes
    nsv6625687copy number variation1nstd224human GRCh37 chr1: 182,543,331-182,579,035 , GRCh38.p12 chr1: 182,574,196-182,609,900 RGS16, RNASEL
    nsv6538365inversion1nstd223human GRCh38 chr1: 178,815,320-184,820,865 , GRCh37.p13 chr1: 178,784,455-184,789,999 NPHS2, COLGALT2, 111 more genes
    nsv6330715copy number variation1nstd223human GRCh38 chr1: 182,577,138-182,578,710 , GRCh37.p13 chr1: 182,546,273-182,547,845 RNASEL
    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
    nsv6297481copy number variation1nstd186human GRCh37 chr1: 182,546,303-182,547,845 , GRCh38.p12 chr1: 182,577,168-182,578,710 RNASEL
    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
    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
    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
    nsv5878860copy number variation1nstd209human GRCh38 chr1: 182,577,138-182,578,709 , GRCh37.p13 chr1: 182,546,273-182,547,844 RNASEL
    nsv5828438copy number variation1nstd209human GRCh38 chr1: 182,577,137-182,578,702 , GRCh37.p13 chr1: 182,546,272-182,547,837 RNASEL
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