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Items: 1 to 20 of 299

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148114copy number variation1nstd102humanUncertain significance GRCh37 chr10: 112,021,329-113,054,313 , GRCh38.p12 chr10: 110,261,571-111,294,555 RBM20, MIR4680, 20 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093858copy number variation1nstd102humanUncertain significance GRCh37 chr10: 111,860,412-112,839,579 , GRCh38.p12 chr10: 110,100,654-111,079,821 LOC105378479, LOC105378482, 22 more genes
    nsv7073198inversion1nstd229human GRCh38 chr10: 109,606,328-111,971,349 , GRCh37.p13 chr10: 111,366,086-113,731,107 LOC105378482, DUSP5, 33 more genes
    nsv7059252inversion1nstd229human GRCh38 chr10: 106,216,129-112,495,031 , GRCh37.p13 chr10: 107,975,887-114,254,790 LOC105378482, DUSP5, 64 more genes
    nsv6895569copy number variation1nstd229human GRCh38 chr10: 110,964,208-110,966,997 , GRCh37.p13 chr10: 112,723,966-112,726,755 SHOC2
    nsv6894615copy number variation1nstd229human GRCh38 chr10: 110,940,201-110,954,300 , GRCh37.p13 chr10: 112,699,959-112,714,058 SHOC2
    nsv6894537copy number variation1nstd229human GRCh38 chr10: 110,986,240-111,000,987 , GRCh37.p13 chr10: 112,745,998-112,760,745 SHOC2, MIR548E
    nsv6891490copy number variation1nstd229human GRCh38 chr10: 110,976,911-110,983,501 , GRCh37.p13 chr10: 112,736,669-112,743,259 SHOC2
    nsv6890453copy number variation1nstd229human GRCh38 chr10: 110,975,001-110,977,900 , GRCh37.p13 chr10: 112,734,759-112,737,658 SHOC2
    nsv6889433copy number variation1nstd229human GRCh38 chr10: 110,995,343-110,999,373 , GRCh37.p13 chr10: 112,755,101-112,759,131 SHOC2
    nsv6887775copy number variation1nstd229human GRCh38 chr10: 110,952,459-111,068,219 , GRCh37.p13 chr10: 112,712,217-112,827,977 SHOC2, MIR548E
    nsv6887705copy number variation1nstd229human GRCh38 chr10: 110,974,329-110,978,282 , GRCh37.p13 chr10: 112,734,087-112,738,040 SHOC2
    nsv6887507copy number variation1nstd229human GRCh38 chr10: 110,295,301-111,328,300 , GRCh37.p13 chr10: 112,055,059-113,088,058 HEAT2, BTBD7P2, 20 more genes
    nsv6885301copy number variation1nstd229human GRCh38 chr10: 110,780,328-116,002,717 , GRCh37.p13 chr10: 112,540,086-116,786,295 UBE2V1P5, MIR6715A, 66 more genes
    nsv6883268copy number variation1nstd229human GRCh38 chr10: 110,976,687-110,979,926 , GRCh37.p13 chr10: 112,736,445-112,739,684 SHOC2
    nsv6881670copy number variation1nstd229human GRCh38 chr10: 110,967,045-110,985,008 , GRCh37.p13 chr10: 112,726,803-112,744,766 SHOC2
    nsv6878703copy number variation1nstd229human GRCh38 chr10: 110,956,015-110,956,763 , GRCh37.p13 chr10: 112,715,773-112,716,521 SHOC2
    nsv6595450inversion1nstd223human GRCh38 chr10: 110,924,793-110,925,752 , GRCh37.p13 chr10: 112,684,551-112,685,510 SHOC2
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