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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073486inversion1nstd229human GRCh38 chr17: 15,622,817-18,740,940 , GRCh37.p13 chr17: 15,526,131-18,644,253 NCOR1, KRT16P6, 129 more genes
    nsv7073439inversion1nstd229human GRCh38 chr17: 15,962,151-19,146,977 , GRCh37.p13 chr17: 15,865,465-19,050,290 RNU6-767P, KRT17P5, 129 more genes
    nsv7066862inversion1nstd229human GRCh38 chr17: 15,664,455-18,717,083 , GRCh37.p13 chr17: 15,567,769-18,620,396 KRT16P6, RPLP1P11, 129 more genes
    nsv7063823inversion1nstd229human GRCh38 chr17: 16,127,666-16,472,211 , GRCh37.p13 chr17: 16,030,980-16,375,525 NCOR1, SNORD163, 13 more genes
    nsv7059660inversion1nstd229human GRCh38 chr17: 16,041,448-17,186,703 , GRCh37.p13 chr17: 15,944,762-17,090,017 SNHG29, ZNF624, 46 more genes
    nsv7059177inversion1nstd229human GRCh38 chr17: 15,493,473-18,338,296 , GRCh37.p13 chr17: 15,396,787-18,241,610 TOM1L2, PPIAP53, 107 more genes
    nsv6998068copy number variation1nstd229human GRCh38 chr17: 16,377,611-16,380,175 , GRCh37.p13 chr17: 16,280,925-16,283,489 UBB
    nsv6997737copy number variation1nstd229human GRCh38 chr17: 16,347,446-16,616,929 , GRCh37.p13 chr17: 16,250,760-16,520,243 SNORD49A, LOC105371554, 11 more genes
    nsv6995851copy number variation1nstd229human GRCh38 chr17: 16,261,589-17,283,740 , GRCh37.p13 chr17: 16,164,903-17,187,054 SRP68P1, SNORD49B, 42 more genes
    nsv6994452copy number variation1nstd229human GRCh38 chr17: 16,355,201-16,380,173 , GRCh37.p13 chr17: 16,258,515-16,283,487 UBB
    nsv6979797copy number variation1nstd229human GRCh38 chr17: 16,368,854-16,586,406 , GRCh37.p13 chr17: 16,272,168-16,489,720 FTLP12, LOC105371554, 8 more genes
    nsv6637693copy number variation1nstd102humanUncertain significance GRCh37 chr17: 15,754,174-16,657,319 , GRCh38.p12 chr17: 15,850,860-16,754,005 SNORD65, RN7SL442P, 29 more genes
    nsv6637557copy number variation1nstd102humanUncertain significance GRCh37 chr17: 15,722,840-16,653,256 , GRCh38.p12 chr17: 15,819,526-16,749,942 RPLP1P11, SNORD49A, 31 more genes
    nsv6593366inversion1nstd223human GRCh38 chr17: 15,604,136-18,759,631 , GRCh37.p13 chr17: 15,507,450-18,662,944 EEF1A1P43, ZNF624, 131 more genes
    nsv6590468inversion1nstd223human GRCh38 chr17: 15,738,295-18,638,514 , GRCh37.p13 chr17: 15,641,609-18,541,827 LOC105371570, RAI1-AS1, 120 more genes
    nsv6587833inversion1nstd223human GRCh38 chr17: 15,680,260-18,702,090 , GRCh37.p13 chr17: 15,583,574-18,605,403 RPLP1P11, KRT16P6, 128 more genes
    nsv6579420inversion1nstd223human GRCh38 chr17: 15,711,972-18,674,503 , GRCh37.p13 chr17: 15,615,286-18,577,816 NOS2P2, LOC105371566, 124 more genes
    nsv6578694inversion1nstd223human GRCh38 chr17: 15,604,091-18,759,630 , GRCh37.p13 chr17: 15,507,405-18,662,943 TRPV2, SNORD49B, 131 more genes
    nsv6315277copy number variation1nstd102humanPathogenic GRCh38 chr17: 11,915,997-17,892,664 , GRCh37.p13 chr17: 11,819,314-17,795,978 LINC02087, USP32P1, 135 more genes
    nsv6315238complex substitution1nstd102humanPathogenic GRCh37 chr17: 14,876,984-22,124,952 , GRCh38.p12 chr17: 14,973,667-22,625,625 ADORA2B, ALDH3A1, 281 more genes
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