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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146007copy number variation1nstd232human GRCh37.p13 chr19: 48,868,620-48,868,697 , GRCh38.p12 chr19: 48,365,363-48,365,440 SYNGR4
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 more genes
    nsv7073220inversion1nstd229human GRCh38 chr19: 45,719,988-49,018,157 , GRCh37.p13 chr19: 46,223,246-49,521,414 RUVBL2, NTN5, 150 more genes
    nsv7064020inversion1nstd229human GRCh38 chr19: 48,004,601-50,148,757 , GRCh37.p13 chr19: 48,507,858-50,652,014 TEAD2, LHB, 155 more genes
    nsv7016555copy number variation1nstd229human GRCh38 chr19: 48,351,837-48,362,304 , GRCh37.p13 chr19: 48,855,094-48,865,561 SYNGR4, TMEM143
    nsv7014397copy number variation1nstd229human GRCh38 chr19: 48,374,924-48,390,128 , GRCh37.p13 chr19: 48,878,181-48,893,385 SYNGR4, KDELR1
    nsv7012452copy number variation1nstd229human GRCh38 chr19: 45,998,776-48,954,957 , GRCh37.p13 chr19: 46,502,034-49,458,214 TMEM160, SNORD23, 131 more genes
    nsv7008905copy number variation1nstd229human GRCh38 chr19: 48,370,387-48,374,881 , GRCh37.p13 chr19: 48,873,644-48,878,138 SYNGR4
    nsv6598038inversion1nstd223human GRCh38 chr19: 45,719,988-49,018,154 , GRCh37.p13 chr19: 46,223,246-49,521,411 PLEKHA4, GAPDHP38, 150 more genes
    nsv6595834inversion1nstd223human GRCh38 chr19: 48,004,600-50,148,749 , GRCh37.p13 chr19: 48,507,857-50,652,006 KDELR1, VRK3, 155 more genes
    nsv6534825copy number variation1nstd223human GRCh38 chr19: 48,362,601-48,366,800 , GRCh37.p13 chr19: 48,865,858-48,870,057 SYNGR4, TMEM143
    nsv6524928copy number variation1nstd223human GRCh38 chr19: 48,367,775-48,368,413 , GRCh37.p13 chr19: 48,871,032-48,871,670 SYNGR4
    nsv6226852copy number variation1nstd214human GRCh38 chr19: 48,365,363-48,365,440 , GRCh37.p13 chr19: 48,868,620-48,868,697 SYNGR4
    nsv6224593copy number variation1nstd214human GRCh38 chr19: 48,365,291-48,365,367 , GRCh37.p13 chr19: 48,868,548-48,868,624 SYNGR4
    nsv6224245copy number variation1nstd214human GRCh38 chr19: 48,365,303-48,365,379 , GRCh37.p13 chr19: 48,868,560-48,868,636 SYNGR4
    nsv6215386copy number variation1nstd214human GRCh38 chr19: 48,365,363-48,365,522 , GRCh37.p13 chr19: 48,868,620-48,868,779 SYNGR4
    nsv6212013copy number variation1nstd214human GRCh38 chr19: 48,365,332-48,365,410 , GRCh37.p13 chr19: 48,868,589-48,868,667 SYNGR4
    nsv6207550copy number variation1nstd214human GRCh38 chr19: 48,365,189-48,365,346 , GRCh37.p13 chr19: 48,868,446-48,868,603 SYNGR4
    nsv6133704copy number variation1nstd213human GRCh37 chr19: 45,030,000-55,230,001 , GRCh38.p12 chr19: 44,525,967-54,071,460 AP2A1, APOC1, 582 more genes
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 more genes
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