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Items: 1 to 20 of 21123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3140557copy number variation1nstd151human GRCh37 chr10: 55,626,399-56,138,707 , GRCh38.p12 chr10: 53,866,639-54,378,947 PCDH15
    nsv3125747copy number variation1nstd151human GRCh37 chr2: 205,550,901-206,058,049 , GRCh38.p12 chr2: 204,686,178-205,193,325 PARD3B
    nsv3153586copy number variation1nstd151human GRCh37 chr10: 68,138,907-68,535,287 , GRCh38.p12 chr10: 66,379,149-66,775,529 CTNNA3
    nsv3141579copy number variation1nstd151human GRCh37 chr10: 68,138,907-68,526,179 , GRCh38.p12 chr10: 66,379,149-66,766,421 CTNNA3
    nsv3118967copy number variation1nstd151human GRCh37 chr1: 225,156,459-225,539,588 , GRCh38.p12 chr1: 224,968,757-225,351,886 DNAH14
    nsv3121017copy number variation1nstd151human GRCh37 chr7: 3,658,709-4,026,959 , GRCh38.p12 chr7: 3,619,077-3,987,327 SDK1
    nsv3157477copy number variation1nstd151human GRCh37 chr10: 68,040,225-68,381,547 , GRCh38.p12 chr10: 66,280,467-66,621,789 CTNNA3
    nsv3151684copy number variation1nstd151human GRCh37 chr11: 83,544,654-83,878,010 , GRCh38.p12 chr11: 83,833,611-84,166,967 DLG2
    nsv3132488copy number variation1nstd151human GRCh37 chr7: 48,237,832-48,564,039 , GRCh38.p12 chr7: 48,198,235-48,524,443 ABCA13
    nsv3143915copy number variation1nstd151human GRCh37 chr10: 32,832,225-33,143,422 , GRCh38.p12 chr10: 32,543,297-32,854,494 CCDC7
    nsv3134499copy number variation1nstd151human GRCh37 chr6: 128,410,832-128,718,838 , GRCh38.p12 chr6: 128,089,687-128,397,693 , GRCh38.p12 chr6|NT_187556.1: 439,021-747,027 PTPRK
    nsv3130998copy number variation1nstd151human GRCh37 chr4: 93,225,805-93,511,442 , GRCh38.p12 chr4: 92,304,654-92,590,291 GRID2
    nsv3130574copy number variation1nstd151human GRCh37 chr6: 101,037,507-101,315,878 , GRCh38.p12 chr6: 100,589,631-100,868,002 ASCC3
    nsv3142145copy number variation1nstd151human GRCh37 chr9: 17,143,283-17,416,192 , GRCh38.p12 chr9: 17,143,285-17,416,194 CNTLN
    nsv3140994copy number variation2nstd151human GRCh37 chr10: 68,280,354-68,535,287 , GRCh38.p12 chr10: 66,520,596-66,775,529 CTNNA3
    nsv3137114copy number variation1nstd151human GRCh37 chr6: 121,401,914-121,655,581 , GRCh38.p12 chr6: 121,080,768-121,334,435 TBC1D32
    nsv3123789copy number variation1nstd151human GRCh37 chr1: 237,729,865-237,982,495 , GRCh38.p12 chr1: 237,566,565-237,819,195 RYR2
    nsv3118745copy number variation1nstd151human GRCh37 chr5: 93,159,851-93,410,461 , GRCh38.p12 chr5: 93,824,145-94,074,756 ARB2A
    nsv3132841copy number variation5nstd151human GRCh37 chr7: 33,945,223-34,192,890 , GRCh38.p12 chr7: 33,905,611-34,153,278 BMPER
    nsv3127643copy number variation1nstd151human GRCh37 chr2: 226,273,595-226,516,284 , GRCh38.p12 chr2: 225,408,879-225,651,568 NYAP2
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