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Items: 1 to 20 of 137

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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
    nsv7093801copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,671,314-79,799,964 , GRCh38.p12 chr10: 73,911,556-78,040,206 COMTD1, DUSP13B, 53 more genes
    nsv7093731copy number variation1nstd102humanPathogenic GRCh37 chr10: 76,349,020-78,317,046 , GRCh38.p12 chr10: 74,589,262-76,557,288 ADK, SAMD8, 25 more genes
    nsv7093650copy number variation1nstd102humanLikely benign GRCh37 chr10: 76,736,352-77,198,536 , GRCh38.p12 chr10: 74,976,594-75,438,778 VDAC2, COMTD1, 16 more genes
    nsv7068569inversion1nstd229human GRCh38 chr10: 75,081,990-75,324,893 , GRCh37.p13 chr10: 76,841,748-77,084,651 HMGA1P5, RPS26P42, 8 more genes
    nsv7063069inversion1nstd229human GRCh38 chr10: 75,019,895-76,543,360 , GRCh37.p13 chr10: 76,779,653-78,303,118 SAMD8, LOC105378367, 21 more genes
    nsv6894636copy number variation1nstd229human GRCh38 chr10: 75,024,032-75,329,494 , GRCh37.p13 chr10: 76,783,790-77,089,252 RPS26P42, DUSP29, 10 more genes
    nsv6893610copy number variation1nstd229human GRCh38 chr10: 75,219,501-75,324,900 , GRCh37.p13 chr10: 76,979,259-77,084,658 HMGA1P5, RPL39P25, 4 more genes
    nsv6890831copy number variation1nstd229human GRCh38 chr10: 75,218,168-75,241,294 , GRCh37.p13 chr10: 76,977,926-77,001,052 VDAC2, COMTD1
    nsv6890105copy number variation1nstd229human GRCh38 chr10: 74,976,594-75,438,778 , GRCh37.p13 chr10: 76,736,352-77,198,536 SNORD172, LOC101929234, 16 more genes
    nsv6637331copy number variation1nstd102humanUncertain significance GRCh37 chr10: 76,763,852-77,101,087 , GRCh38.p12 chr10: 75,004,094-75,341,329 KAT6B, SNORD172, 11 more genes
    nsv6620679copy number variation1nstd224human GRCh37 chr10: 76,986,741-77,073,351 , GRCh38.p12 chr10: 75,226,983-75,313,593 VDAC2, ZNF503, 4 more genes
    nsv6589287inversion1nstd223human GRCh38 chr10: 75,081,989-75,324,890 , GRCh37.p13 chr10: 76,841,747-77,084,648 ZNF503-AS1, RPL39P25, 8 more genes
    nsv6454439copy number variation1nstd223human GRCh38 chr10: 75,024,032-75,329,491 , GRCh37.p13 chr10: 76,783,790-77,089,249 DUSP29, RPL39P25, 10 more genes
    nsv6314185copy number variation1nstd102humanPathogenic GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956 SLC25A16, CTNNA3, 204 more genes
    nsv6132051copy number variation1nstd213human GRCh37 chr10: 76,880,000-77,230,001 , GRCh38.p12 chr10: 75,120,242-75,470,243 VDAC2, LRMDA, 11 more genes
    nsv6132012copy number variation1nstd213human GRCh37 chr10: 76,928,627-77,029,502 , GRCh38.p12 chr10: 75,168,869-75,269,744 VDAC2, COMTD1, 2 more genes
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5302472copy number variation1nstd204human GRCh37.p13 chr10: 76,991,199-76,992,547 , GRCh38.p13 chr10: 75,231,441-75,232,789 VDAC2, COMTD1
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