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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139171insertion1nstd232human GRCh37.p13 chr17: 47,780,657-47,780,657 , GRCh38.p12 chr17: 49,703,295-49,703,295 SLC35B1
    nsv7058619inversion1nstd229human GRCh38 chr17: 49,389,100-51,159,770 , GRCh37.p13 chr17: 47,466,462-49,237,131 H1-9P, FLJ45513, 59 more genes
    nsv6986384copy number variation1nstd229human GRCh38 chr17: 49,089,556-55,863,152 , GRCh37.p13 chr17: 47,166,918-53,940,513 LOC107985002, FAM117A, 107 more genes
    nsv6624091copy number variation1nstd224human GRCh37 chr17: 47,685,050-47,992,476 , GRCh38.p12 chr17: 49,607,688-49,915,112 SPOP, SLC35B1, 5 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5529562copy number variation1nstd206human GRCh38 chr17: 49,703,610-49,703,881 , GRCh37.p13 chr17: 47,780,972-47,781,243 SLC35B1
    nsv5358923translocation1nstd200human GRCh38 chr17: 49,703,257-49,703,257 , GRCh38 chr17: 49,698,735-49,698,735 , GRCh37.p13 chr17: 47,776,097-47,776,097 , GRCh37.p13 chr17: 47,780,619-47,780,619 SLC35B1
    nsv5294128copy number variation1nstd204human GRCh38.p13 chr17: 49,634,301-49,749,400 , GRCh37.p13 chr17: 47,711,663-47,826,762 FAM117A, SPOP, 1 more genes
    nsv5013800copy number variation1nstd200human GRCh38 chr17: 49,703,610-49,703,881 , GRCh37.p13 chr17: 47,780,972-47,781,243 SLC35B1
    nsv4864706copy number variation1nstd200human GRCh37 chr17: 47,780,972-47,781,243 , GRCh38.p12 chr17: 49,703,610-49,703,881 SLC35B1
    nsv4676234copy number variation1nstd102humanUncertain significance GRCh37 chr17: 47,689,783-47,791,730 , GRCh38.p12 chr17: 49,612,421-49,714,368 LOC107984999, FAM117A, 2 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv3921455copy number variation1nstd102humanPathogenic NCBI36 chr17: 44,793,516-45,701,800 , GRCh37 chr17: 47,438,517-48,346,801 , GRCh38 chr17: 49,361,155-50,269,440 DLX4, H1-9P, 32 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
    nsv3912763copy number variation1nstd102humanPathogenic NCBI36 chr17: 44,570,225-47,580,169 , GRCh37 chr17: 47,215,226-50,225,170 , GRCh38 chr17: 49,137,864-52,147,810 CACNA1G, SUMO2P7, 77 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 more genes
    nsv3911563copy number variation1nstd102humanPathogenic NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214 PLEKHH3, CHCT1, 958 more genes
    nsv3909511copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846 FOXK2, SOCS3-DT, 958 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
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