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Items: 1 to 20 of 210

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112771copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,098,196-15,442,500 , GRCh38.p12 chr17: 14,194,879-15,539,186 CDRT8, TVP23C, 24 more genes
    nsv5533691copy number variation1nstd206human GRCh38 chr17: 15,106,354-15,108,718 , GRCh37.p13 chr17: 15,009,671-15,012,035 CDRT8
    nsv5523921copy number variation1nstd206human GRCh38 chr17: 15,072,380-15,104,010 , GRCh37.p13 chr17: 14,975,697-15,007,327 CDRT8
    nsv5520330copy number variation1nstd206human GRCh38 chr17: 14,022,600-15,889,111 , GRCh37.p13 chr17: 13,925,917-15,792,425 CDRT15, CDRT7, 42 more genes
    nsv5515756copy number variation1nstd206human GRCh38 chr17: 15,092,454-15,154,158 , GRCh37.p13 chr17: 14,995,771-15,057,475 CDRT8, LOC107984976
    nsv5381804copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,100,118-15,455,297 , GRCh38.p12 chr17: 14,196,801-15,551,983 LOC105371547, TVP23C-CDRT4, 24 more genes
    nsv5025987copy number variation1nstd200human GRCh38 chr17: 14,635,906-15,104,798 , GRCh37.p13 chr17: 14,539,223-15,008,115 CDRT7, CDRT8, 5 more genes
    nsv4858159copy number variation1nstd200human GRCh37 chr17: 14,975,697-15,007,327 , GRCh38.p12 chr17: 15,072,380-15,104,010 CDRT8
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729887copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr17: 14,111,754-15,442,178 , GRCh38.p12 chr17: 14,208,437-15,538,864 CDRT15, LINC02096, 24 more genes
    nsv4684248copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,079,630-15,370,444 , GRCh38.p12 chr17: 14,176,313-15,467,130 MIR4731, LOC107984996, 21 more genes
    nsv4684245copy number variation1nstd102humanUncertain significance GRCh37 chr17: 10,493,837-15,099,023 , GRCh38.p12 chr17: 10,590,520-15,195,706 LOC100506974, MIR1269B, 52 more genes
    nsv4680571copy number variation1nstd189human GRCh37.p13 chr17: 14,098,278-15,484,871 , GRCh38.p12 chr17: 14,194,961-15,581,557 COX10, PMP22, 25 more genes
    nsv4680027copy number variation1nstd189human GRCh37.p13 chr17: 14,100,654-15,486,881 , GRCh38.p12 chr17: 14,197,337-15,583,567 COX10, PMP22, 25 more genes
    nsv4675278copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,195,642-15,545,880 , GRCh38.p12 chr17: 14,292,325-15,642,566 LOC107984996, LOC107984976, 24 more genes
    nsv4669429copy number variation1nstd186human GRCh37 chr17: 14,668,589-15,084,842 , GRCh38.p12 chr17: 14,765,272-15,181,525 CDRT7, CDRT8, 6 more genes
    nsv4621486copy number variation1nstd183human GRCh37 chr17: 14,082,958-15,484,871 , GRCh38.p12 chr17: 14,179,641-15,581,557 RPL9P2, FBXW10B, 25 more genes
    nsv4578264copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,111,772-15,442,066 , GRCh38.p12 chr17: 14,208,455-15,538,752 CDRT8, PPIAP53, 24 more genes
    nsv4532018copy number variation1nstd166human GRCh37.p13 chr17: 14,093,499-15,486,000 , GRCh38.p12 chr17: 14,190,182-15,582,686 TVP23C, LOC101928475, 25 more genes
    nsv4530845copy number variation1nstd166human GRCh37.p13 chr17: 14,096,997-15,486,650 , GRCh38.p12 chr17: 14,193,680-15,583,336 TVP23C, PPIAP53, 25 more genes
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