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Items: 1 to 20 of 236

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148155copy number variation1nstd102humanPathogenic GRCh37 chr17: 72,718,277-74,142,256 , GRCh38.p12 chr17: 74,722,138-76,146,175 TRIM65, TEN1, 74 more genes
    nsv7098900copy number variation1nstd102humanUncertain significance GRCh37 chr17: 72,864,876-73,328,878 , GRCh38.p12 chr17: 74,868,753-75,332,797 CDR2L, OTOP2, 28 more genes
    nsv7067990inversion1nstd229human GRCh38 chr17: 75,113,953-75,113,974 , GRCh37.p13 chr17: 73,110,048-73,110,069 ARMC7
    nsv6997609copy number variation1nstd229human GRCh38 chr17: 75,114,668-75,123,555 , GRCh37.p13 chr17: 73,110,763-73,119,650 ARMC7
    nsv6997214copy number variation1nstd229human GRCh38 chr17: 75,106,036-75,110,289 , GRCh37.p13 chr17: 73,102,131-73,106,384 ARMC7, SLC16A5
    nsv6995629copy number variation1nstd229human GRCh38 chr17: 75,123,412-75,123,588 , GRCh37.p13 chr17: 73,119,507-73,119,683 ARMC7
    nsv6994090copy number variation1nstd229human GRCh38 chr17: 75,053,032-75,108,705 , GRCh37.p13 chr17: 73,049,127-73,104,800 SLC16A5, TRIM80P, 2 more genes
    nsv6991504copy number variation1nstd229human GRCh38 chr17: 75,114,177-75,118,055 , GRCh37.p13 chr17: 73,110,272-73,114,150 ARMC7
    nsv6989542copy number variation1nstd229human GRCh38 chr17: 75,111,471-75,115,291 , GRCh37.p13 chr17: 73,107,566-73,111,386 ARMC7
    nsv6987172copy number variation1nstd229human GRCh38 chr17: 75,118,291-75,122,782 , GRCh37.p13 chr17: 73,114,386-73,118,877 ARMC7
    nsv6984494copy number variation1nstd229human GRCh38 chr17: 75,111,651-75,112,143 , GRCh37.p13 chr17: 73,107,746-73,108,238 ARMC7
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6980042copy number variation1nstd229human GRCh38 chr17: 75,121,529-75,123,829 , GRCh37.p13 chr17: 73,117,624-73,119,924 ARMC7
    nsv6978514copy number variation1nstd229human GRCh38 chr17: 75,115,427-75,117,874 , GRCh37.p13 chr17: 73,111,522-73,113,969 ARMC7
    nsv6624308copy number variation1nstd224human GRCh37 chr17: 72,877,346-73,127,348 , GRCh38.p12 chr17: 74,881,216-75,131,253 SLC16A5, KCTD2, 18 more genes
    nsv6590779inversion1nstd223human GRCh38 chr17: 75,121,753-75,122,124 , GRCh37.p13 chr17: 73,117,848-73,118,219 ARMC7
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6530995copy number variation1nstd223human GRCh38 chr17: 75,111,633-75,112,143 , GRCh37.p13 chr17: 73,107,728-73,108,238 ARMC7
    nsv6525776copy number variation1nstd223human GRCh38 chr17: 75,111,471-75,115,291 , GRCh37.p13 chr17: 73,107,566-73,111,386 ARMC7
    nsv6521984copy number variation1nstd223human GRCh38 chr17: 75,113,041-75,113,357 , GRCh37.p13 chr17: 73,109,136-73,109,452 ARMC7
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