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Items: 1 to 20 of 10884

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4376169copy number variation1nstd173human GRCh37 chr7: 125,231,958-125,714,003 , GRCh38.p12 chr7: 125,591,904-126,073,949 LOC105375487
    nsv4366566copy number variation1nstd173human GRCh37 chr7: 125,235,254-125,714,003 , GRCh38.p12 chr7: 125,595,200-126,073,949 LOC105375487
    nsv4387057copy number variation1nstd173human GRCh37 chr18: 70,622,593-70,967,818 , GRCh38.p12 chr18: 72,955,358-73,300,583 LINC02864
    nsv4386347copy number variation1nstd173human GRCh37 chr7: 125,082,275-125,419,585 , GRCh38.p12 chr7: 125,442,221-125,779,531 LOC100506664
    nsv4386310copy number variation2nstd173human GRCh37 chr9: 11,734,178-12,071,041 , GRCh38.p12 chr9: 11,734,178-12,071,041 LOC101929446
    nsv4373984copy number variation3nstd173human GRCh37 chr13: 55,138,222-55,474,506 , GRCh38.p12 chr13: 54,564,087-54,900,371 LOC105370213
    nsv4375715copy number variation1nstd173human GRCh37 chr18: 70,622,593-70,958,283 , GRCh38.p12 chr18: 72,955,358-73,291,048 LINC02864
    nsv4367096copy number variation2nstd173human GRCh37 chr13: 55,143,469-55,474,506 , GRCh38.p12 chr13: 54,569,334-54,900,371 LOC105370213
    nsv4387459copy number variation1nstd173human GRCh37 chr4: 35,572,506-35,903,030 , GRCh38.p12 chr4: 35,570,884-35,901,408 LOC105374396
    nsv4385861copy number variation1nstd173human GRCh37 chr4: 35,575,710-35,903,030 , GRCh38.p12 chr4: 35,574,088-35,901,408 LOC105374396
    nsv4387288copy number variation1nstd173human GRCh37 chr10: 68,253,277-68,564,867 , GRCh38.p12 chr10: 66,493,519-66,805,109 CTNNA3
    nsv4367054copy number variation1nstd173human GRCh37 chr10: 68,258,924-68,564,867 , GRCh38.p12 chr10: 66,499,166-66,805,109 CTNNA3
    nsv4375253copy number variation2nstd173human GRCh37 chrY: 22,214,486-22,518,330 , GRCh38.p12 chrY: 20,052,600-20,356,444 ZNF884P
    nsv4374231copy number variation1nstd173human GRCh37 chr2: 137,923,090-138,226,066 , GRCh38.p12 chr2: 137,165,520-137,468,496 THSD7B
    nsv4372743copy number variation1nstd173human GRCh37 chr2: 137,923,078-138,225,635 , GRCh38.p12 chr2: 137,165,508-137,468,065 THSD7B
    nsv4382261copy number variation1nstd173human GRCh37 chr2: 137,923,212-138,225,635 , GRCh38.p12 chr2: 137,165,642-137,468,065 THSD7B
    nsv4376153copy number variation1nstd173human GRCh37 chr10: 55,819,471-56,110,079 , GRCh38.p12 chr10: 54,059,711-54,350,319 PCDH15
    nsv4378536copy number variation1nstd173human GRCh37 chr10: 68,213,165-68,502,588 , GRCh38.p12 chr10: 66,453,407-66,742,830 CTNNA3
    nsv4371180copy number variation3nstd173human GRCh37 chr9: 11,782,269-12,071,041 , GRCh38.p12 chr9: 11,782,269-12,071,041 LOC101929446
    nsv4365183copy number variation1nstd173human GRCh37 chr9: 11,645,688-11,934,376 , GRCh38.p12 chr9: 11,645,688-11,934,376 LOC101929446
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