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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3110282copy number variation1nstd145human GRCh37 chr14: 41,610,669-41,667,552 , GRCh38.p12 chr14: 41,141,466-41,198,349 LINC02315
    nsv3118081copy number variation72nstd145human GRCh37 chr7: 141,766,533-141,793,377 , GRCh38.p12 chr7|NT_187562.1: 28,613-55,457 , GRCh38.p12 chr7: 142,066,733-142,093,577 MGAM
    nsv3110467copy number variation2nstd145human GRCh37 chr6: 163,408,073-163,431,184 , GRCh38.p12 chr6: 162,987,041-163,010,152 PACRG
    nsv3114031copy number variation1nstd145human GRCh37 chr5: 116,287,293-116,302,566 , GRCh38.p12 chr5: 116,951,597-116,966,870 LOC105379137
    nsv3117451copy number variation18nstd145human GRCh37 chr6: 80,557,220-80,570,188 , GRCh38.p12 chr6: 79,847,503-79,860,471 LOC100422671
    nsv3111509copy number variation29nstd145human GRCh37 chr8: 2,150,517-2,161,441 , GRCh38.p12 chr8|NT_187576.1: 385,727-396,651 , GRCh38.p12 chr8: 2,202,878-2,213,774 LOC105377782
    nsv3114521copy number variation39nstd145human GRCh37 chr18: 66,745,828-66,756,183 , GRCh38.p12 chr18: 69,078,591-69,088,946 CCDC102B
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3110942copy number variation60nstd145human GRCh37 chr7: 91,033,585-91,042,496 , GRCh38.p12 chr7: 91,404,270-91,413,181 LINC02932
    nsv3115609copy number variation20nstd145human GRCh37 chr1: 222,373,920-222,382,729 , GRCh38.p12 chr1: 222,200,578-222,209,387 CFAP144P3
    nsv3117259copy number variation1nstd145human GRCh37 chr15: 35,237,111-35,245,317 , GRCh38.p12 chr15: 34,944,910-34,953,116 AQR
    nsv3112636copy number variation1nstd145human GRCh37 chr6: 3,712,730-3,719,520 , GRCh38.p12 chr6: 3,712,496-3,719,286 LOC100507336
    nsv3118214copy number variation1nstd145human GRCh37 chr3: 195,137,195-195,143,973 , GRCh38.p12 chr3: 195,416,466-195,423,244 ACAP2
    nsv3117297copy number variation80nstd145human GRCh37 chr7: 154,392,836-154,399,317 , GRCh38.p12 chr7: 154,601,126-154,607,607 DPP6
    nsv3110722copy number variation1nstd145human GRCh37 chr22: 22,358,136-22,364,548 , GRCh38.p12 chr22: 22,003,738-22,010,150 PRAMENP
    nsv3112895copy number variation76nstd145human GRCh37 chr12: 43,020,941-43,027,293 , GRCh38.p12 chr12: 42,627,139-42,633,491 LINC02402
    nsv3112146copy number variation37nstd145human GRCh37 chr11: 93,695,236-93,701,577 , GRCh38.p12 chr11: 93,962,070-93,968,411 LOC101060084
    nsv3111671copy number variation13nstd145human GRCh37 chr8: 2,079,164-2,085,288 , GRCh38.p12 chr8: 2,131,176-2,137,301 , GRCh38.p12 chr8|NT_187576.1: 314,374-320,498 MYOM2
    nsv3116854copy number variation1nstd145human GRCh37 chr17: 4,706,526-4,712,609 , GRCh38.p12 chr17: 4,803,231-4,809,314 PLD2
    nsv3112342copy number variation1nstd145human GRCh37 chr9: 98,266,741-98,272,631 , GRCh38.p12 chr9: 95,504,459-95,510,349 PTCH1
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