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Items: 1 to 20 of 331

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7076518inversion1nstd229human GRCh38 chr10: 68,329,175-68,329,222 , GRCh37.p13 chr10: 70,088,932-70,088,979 PBLD
    nsv7066606inversion1nstd229human GRCh38 chr10: 67,967,096-68,456,909 , GRCh37.p13 chr10: 69,726,853-70,216,666 MYPN, RUFY2, 12 more genes
    nsv6895171copy number variation1nstd229human GRCh38 chr10: 68,286,354-68,293,160 , GRCh37.p13 chr10: 70,046,111-70,052,917 PBLD
    nsv6894591copy number variation1nstd229human GRCh38 chr10: 68,308,470-68,310,887 , GRCh37.p13 chr10: 70,068,227-70,070,644 PBLD
    nsv6889279copy number variation1nstd229human GRCh38 chr10: 68,316,548-68,321,078 , GRCh37.p13 chr10: 70,076,305-70,080,835 PBLD
    nsv6882990copy number variation1nstd229human GRCh38 chr10: 68,321,385-68,329,201 , GRCh37.p13 chr10: 70,081,142-70,088,958 PBLD
    nsv6637795copy number variation1nstd102humanUncertain significance GRCh37 chr10: 69,824,933-70,064,085 , GRCh38.p12 chr10: 68,065,176-68,304,328 MYPN, KRT19P4, 6 more genes
    nsv6637232copy number variation1nstd102humanUncertain significance GRCh37 chr10: 69,824,933-70,070,858 , GRCh38.p12 chr10: 68,065,176-68,311,101 HERC4, PBLD, 6 more genes
    nsv6592955inversion1nstd223human GRCh38 chr10: 68,319,405-68,319,939 , GRCh37.p13 chr10: 70,079,162-70,079,696 PBLD
    nsv6589558inversion1nstd223human GRCh38 chr10: 68,299,609-68,300,164 , GRCh37.p13 chr10: 70,059,366-70,059,921 PBLD
    nsv6585801inversion1nstd223human GRCh38 chr10: 68,324,996-68,326,216 , GRCh37.p13 chr10: 70,084,753-70,085,973 PBLD
    nsv6583740inversion1nstd223human GRCh38 chr10: 68,286,401-68,286,874 , GRCh37.p13 chr10: 70,046,158-70,046,631 PBLD
    nsv6576934inversion1nstd223human GRCh38 chr10: 68,324,311-68,325,060 , GRCh37.p13 chr10: 70,084,068-70,084,817 PBLD
    nsv6576888inversion1nstd223human GRCh38 chr10: 68,311,487-68,312,611 , GRCh37.p13 chr10: 70,071,244-70,072,368 PBLD
    nsv6575907inversion1nstd223human GRCh38 chr10: 68,324,655-68,325,128 , GRCh37.p13 chr10: 70,084,412-70,084,885 PBLD
    nsv6453339copy number variation1nstd223human GRCh38 chr10: 68,308,470-68,310,887 , GRCh37.p13 chr10: 70,068,227-70,070,644 PBLD
    nsv6451400copy number variation1nstd223human GRCh38 chr10: 68,308,601-68,310,700 , GRCh37.p13 chr10: 70,068,358-70,070,457 PBLD
    nsv6450721copy number variation1nstd223human GRCh38 chr10: 68,320,770-68,321,073 , GRCh37.p13 chr10: 70,080,527-70,080,830 PBLD
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