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Items: 1 to 20 of 102

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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
    nsv6893948copy number variation1nstd229human GRCh38 chr10: 110,286,801-110,289,400 , GRCh37.p13 chr10: 112,046,559-112,049,158 SMNDC1, MXI1
    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
    nsv6882125copy number variation1nstd229human GRCh38 chr10: 110,304,201-110,310,700 , GRCh37.p13 chr10: 112,063,959-112,070,458 SMNDC1
    nsv6449009copy number variation1nstd223human GRCh38 chr10: 110,304,401-110,304,800 , GRCh37.p13 chr10: 112,064,159-112,064,558 SMNDC1
    nsv6438196copy number variation1nstd223human GRCh38 chr10: 110,297,801-110,308,500 , GRCh37.p13 chr10: 112,057,559-112,068,258 SMNDC1
    nsv6314085copy number variation1nstd102humanPathogenic GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639 LOC107984268, DPYSL4, 379 more genes
    nsv6308977copy number variation1nstd102humanUncertain significance GRCh37 chr10: 111,860,412-112,404,423 , GRCh38.p12 chr10: 110,100,654-110,644,665 HMGB3P5, SMNDC1, 12 more genes
    nsv6290874copy number variation1nstd102humanUncertain significance GRCh37 chr10: 107,092,654-117,852,548 , GRCh38.p12 chr10: 105,332,896-116,093,037 MIR6715B, SNRPGP12, 118 more genes
    nsv6131764copy number variation1nstd213human GRCh37 chr10: 111,860,000-112,080,001 , GRCh38.p12 chr10: 110,100,242-110,320,243 ADD3, MXI1, 4 more genes
    nsv6131763copy number variation1nstd213human GRCh37 chr10: 110,950,000-112,790,001 , GRCh38.p12 chr10: 109,190,242-111,030,243 XPNPEP1, RNU4-5P, 30 more genes
    nsv6081475insertion1nstd212human GRCh38 chr10: 110,295,559-110,295,559 , GRCh37.p13 chr10: 112,055,317-112,055,317 SMNDC1
    nsv5134188mobile element insertion1nstd203human GRCh38 chr10: 110,290,951-110,290,967 , GRCh37.p13 chr10: 112,050,709-112,050,725 SMNDC1
    nsv4611833copy number variation1nstd183human GRCh37 chr10: 112,063,209-112,069,164 , GRCh38.p12 chr10: 110,303,451-110,309,406 SMNDC1
    nsv4348764copy number variation1nstd102humanPathogenic GRCh37 chr10: 110,022,170-135,439,095 , GRCh38.p12 chr10: 108,262,412-133,625,591 LOC105378492, VENTX, 373 more genes
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