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Items: 1 to 20 of 212

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7060527inversion1nstd229human GRCh38 chr17: 43,542,072-43,634,371 , GRCh37.p13 chr17: 41,619,440-41,711,739 DHX8, ETV4
    nsv6993790copy number variation1nstd229human GRCh38 chr17: 43,537,972-43,541,627 , GRCh37.p13 chr17: 41,615,340-41,618,995 DHX8, ETV4
    nsv6991508copy number variation1nstd229human GRCh38 chr17: 42,821,629-43,873,068 , GRCh37.p13 chr17: 40,973,647-41,950,436 RND2, LOC107985077, 50 more genes
    nsv6984951copy number variation1nstd229human GRCh38 chr17: 43,526,101-43,532,055 , GRCh37.p13 chr17: 41,603,469-41,609,423 ETV4, DHX8
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6981860copy number variation1nstd229human GRCh38 chr17: 43,082,682-43,532,646 , GRCh37.p13 chr17: 41,234,699-41,610,014 MIR2117HG, RNU6-1137P, 20 more genes
    nsv6981457copy number variation1nstd229human GRCh38 chr17: 43,400,201-43,562,200 , GRCh37.p13 chr17: 41,477,569-41,639,568 MIR2117, MIR2117HG, 7 more genes
    nsv6511732copy number variation1nstd223human GRCh38 chr17: 43,537,972-43,541,624 , GRCh37.p13 chr17: 41,615,340-41,618,992 DHX8, ETV4
    nsv6504599copy number variation1nstd223human GRCh38 chr17: 43,439,586-43,590,786 , GRCh37.p13 chr17: 41,516,954-41,668,154 ETV4, RPL29P31, 5 more genes
    nsv6504040copy number variation1nstd223human GRCh38 chr17: 43,537,515-43,634,172 , GRCh37.p13 chr17: 41,614,883-41,711,540 DHX8, ETV4
    nsv6314057copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,202,796-41,974,964 , GRCh38.p12 chr17: 43,050,779-43,897,596 TMEM106A, MPP2, 33 more genes
    nsv5947327copy number variation1nstd209human GRCh38 chr17: 43,545,194-43,545,937 , GRCh37.p13 chr17: 41,622,562-41,623,305 ETV4, DHX8
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5016483copy number variation1nstd200human GRCh38 chr17: 43,545,829-43,546,019 , GRCh37.p13 chr17: 41,623,197-41,623,387 ETV4
    nsv5013724copy number variation1nstd200human GRCh38 chr17: 43,313,216-43,589,560 , GRCh37.p13 chr17: 41,390,570-41,666,928 RNU6-971P, ARL4D, 11 more genes
    nsv4864660copy number variation1nstd200human GRCh37 chr17: 41,390,570-41,666,928 , GRCh38.p12 chr17: 43,313,216-43,589,560 ARL4D, DHX8, 11 more genes
    nsv4729870copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,221,565-41,775,043 , GRCh38.p12 chr17: 43,069,548-43,697,675 LOC105371785, RNU6-406P, 24 more genes
    nsv4680708copy number variation1nstd189human GRCh37.p13 chr17: 41,357,686-42,167,307 , GRCh38.p12 chr17: 43,205,667-44,089,939 , ARL4D, 41 more genes
    nsv4675549copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,399,892-41,736,186 , GRCh38.p12 chr17: 43,322,528-43,658,818 DHX8, RNU6-1137P, 12 more genes
    nsv4674980copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,399,892-42,125,780 , GRCh38.p12 chr17: 43,322,528-44,048,412 RPL29P31, MEOX1, 34 more genes
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