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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148226copy number variation1nstd102humanUncertain significance GRCh38 chr17: 50,169,242-50,170,421 , GRCh37.p13 chr17: 48,246,603-48,247,782 SGCA, H1-9P
    nsv7094979copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr17: 48,068,881-48,278,874 , GRCh38.p12 chr17: 49,991,517-50,201,513 PICART1, H1-9P, 8 more genes
    nsv7094900copy number variation1nstd102humanPathogenic GRCh37 chr17: 48,252,598-48,277,328 , GRCh38.p12 chr17: 50,175,237-50,199,967 SGCA, COL1A1
    nsv7094899copy number variation1nstd102humanPathogenic GRCh37 chr17: 48,243,336-48,246,625 , GRCh38.p12 chr17: 50,165,975-50,169,264 LOC105371818, SGCA
    nsv7058619inversion1nstd229human GRCh38 chr17: 49,389,100-51,159,770 , GRCh37.p13 chr17: 47,466,462-49,237,131 H1-9P, FLJ45513, 59 more genes
    nsv6995118copy number variation1nstd229human GRCh38 chr17: 50,173,271-50,177,675 , GRCh37.p13 chr17: 48,250,632-48,255,036 SGCA
    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
    nsv6310391copy number variation1nstd102humanPathogenic GRCh37 chr17: 48,243,336-48,253,303 , GRCh38.p12 chr17: 50,165,975-50,175,942 LOC105371818, H1-9P, 1 more genes
    nsv6310390copy number variation1nstd102humanPathogenic GRCh37 chr17: 48,243,138-48,245,027 , GRCh38.p12 chr17: 50,165,777-50,167,666 SGCA, LOC105371818
    nsv6310312copy number variation1nstd102humanUncertain significance GRCh37 chr17: 48,243,402-48,278,874 , GRCh38.p12 chr17: 50,166,041-50,201,513 SGCA, H1-9P, 2 more genes
    nsv6310180copy number variation1nstd102humanUncertain significance GRCh37 chr17: 48,252,608-48,253,303 , GRCh38.p12 chr17: 50,175,247-50,175,942 SGCA
    nsv6133066copy number variation1nstd213human GRCh37 chr17: 48,190,000-48,270,001 , GRCh38.p12 chr17: 50,112,636-50,192,640 COL1A1, PDK2, 5 more genes
    nsv6035376copy number variation1nstd212human GRCh38 chr17: 50,166,769-50,166,829 , GRCh37.p13 chr17: 48,244,130-48,244,190 LOC105371818, SGCA
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5026379copy number variation1nstd200human GRCh38 chr17: 50,167,644-50,167,907 , GRCh37.p13 chr17: 48,245,005-48,245,268 SGCA
    nsv4867253copy number variation1nstd200human GRCh37 chr17: 48,245,005-48,245,268 , GRCh38.p12 chr17: 50,167,644-50,167,907 SGCA
    nsv4745026copy number variation1nstd199human GRCh37 chr17: 48,244,057-48,244,158 , GRCh38.p12 chr17: 50,166,696-50,166,797 SGCA, LOC105371818
    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
    nsv3920880copy number variation1nstd102humanPathogenic GRCh38 chr17: 49,974,533-56,807,609 , NCBI36 chr17: 45,406,896-52,239,969 , GRCh37 chr17: 48,051,897-54,884,970 LOC107984983, LOC102724732, 85 more genes
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