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Items: 1 to 20 of 81

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3112094copy number variation94nstd145human GRCh37 chr7: 133,785,285-133,797,218 , GRCh38.p12 chr7: 134,100,532-134,112,465
    nsv3110986copy number variation37nstd145human GRCh37 chr5: 17,640,200-17,651,341 , GRCh38.p12 chr5: 17,640,091-17,651,232 LOC391768
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3116244copy number variation3nstd145human GRCh37 chr22: 37,137,748-37,146,950 , GRCh38.p12 chr22: 36,741,703-36,750,906 CACNG2-DT
    nsv3115130copy number variation1nstd145human GRCh37 chr15: 29,897,155-29,905,835 , GRCh38.p12 chr15: 29,604,951-29,613,631 , GRCh38.p12 chr15|NT_187660.1: 1,889,066-1,897,752 , GRCh38.p12 chr15|NW_011332701.1: 1,776,582-1,785,268 TUBBP8
    nsv3113832copy number variation1nstd145human GRCh37 chr17: 65,419,244-65,426,237 , GRCh38.p12 chr17: 67,423,128-67,430,121 PITPNC1
    nsv3112895copy number variation76nstd145human GRCh37 chr12: 43,020,941-43,027,293 , GRCh38.p12 chr12: 42,627,139-42,633,491 LINC02402
    nsv3117385copy number variation76nstd145human GRCh37 chr7: 110,182,897-110,188,346 , GRCh38.p12 chr7: 110,542,840-110,548,289 LOC105375451
    nsv3115418copy number variation2nstd145human GRCh37 chr1: 174,796,674-174,801,989 , GRCh38.p12 chr1: 174,827,536-174,832,851 RABGAP1L
    nsv3112322copy number variation1nstd145human GRCh37 chr4: 79,353,722-79,358,668 , GRCh38.p12 chr4: 78,432,568-78,437,514 FRAS1
    nsv3114178copy number variation107nstd145human GRCh37 chr6: 53,928,991-53,933,879 , GRCh38.p12 chr6: 54,064,193-54,069,081 MLIP
    nsv3117729copy number variation1nstd145human GRCh37 chr12: 129,625,471-129,630,048 , GRCh38.p12 chr12: 129,140,926-129,145,503 TMEM132D
    nsv3114222copy number variation54nstd145human GRCh37 chr12: 82,139,806-82,144,215 , GRCh38.p12 chr12: 81,746,027-81,750,436 PPFIA2
    nsv3112692copy number variation29nstd145human GRCh37 chr3: 131,708,301-131,712,626 , GRCh38.p12 chr3: 131,989,457-131,993,782 CPNE4
    nsv3117963copy number variation1nstd145human GRCh37 chr7: 80,532,246-80,536,557 , GRCh38.p12 chr7: 80,902,930-80,907,241 SEMA3C
    nsv3112110copy number variation12nstd145human GRCh37 chr4: 106,940,561-106,944,506 , GRCh38.p12 chr4: 106,019,404-106,023,349 LOC101929577
    nsv3116345copy number variation23nstd145human GRCh37 chr11: 58,632,160-58,635,965 , GRCh38.p12 chr11: 58,864,687-58,868,492 GLYATL2
    nsv3113930copy number variation1nstd145human GRCh37 chr2: 209,672,190-209,675,968 , GRCh38.p12 chr2: 208,807,466-208,811,244 LOC101927960
    nsv3117571copy number variation81nstd145human GRCh37 chr11: 107,239,191-107,242,941 , GRCh38.p12 chr11: 107,368,465-107,372,215 CWF19L2
    nsv3114451copy number variation90nstd145human GRCh37 chr12: 90,487,994-90,491,654 , GRCh38.p12 chr12: 90,094,217-90,097,877 LOC105369890
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