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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075849inversion1nstd229human GRCh38 chr14: 32,120,900-32,120,936 , GRCh37.p13 chr14: 32,590,106-32,590,142 ARHGAP5
    nsv7075358inversion1nstd229human GRCh38 chr14: 32,120,865-32,120,906 , GRCh37.p13 chr14: 32,590,071-32,590,112 ARHGAP5
    nsv7072225inversion1nstd229human GRCh38 chr14: 31,291,623-36,485,208 , GRCh37.p13 chr14: 31,760,829-36,954,413 LOC101927178, RNU7-93P, 84 more genes
    nsv7060636inversion1nstd229human GRCh38 chr14: 32,155,500-32,163,072 , GRCh37.p13 chr14: 32,624,706-32,632,278 ARHGAP5
    nsv6957897copy number variation1nstd229human GRCh38 chr14: 32,118,014-32,122,947 , GRCh37.p13 chr14: 32,587,220-32,592,153 ARHGAP5
    nsv6952687copy number variation1nstd229human GRCh38 chr14: 32,128,701-32,164,500 , GRCh37.p13 chr14: 32,597,907-32,633,706 ARHGAP5
    nsv6951125copy number variation1nstd229human GRCh38 chr14: 32,138,158-32,138,276 , GRCh37.p13 chr14: 32,607,364-32,607,482 ARHGAP5
    nsv6947952copy number variation1nstd229human GRCh38 chr14: 32,070,205-32,072,942 , GRCh37.p13 chr14: 32,539,411-32,542,148 ARHGAP5
    nsv6947649copy number variation1nstd229human GRCh38 chr14: 32,120,301-32,124,252 , GRCh37.p13 chr14: 32,589,507-32,593,458 ARHGAP5
    nsv6947320copy number variation1nstd229human GRCh38 chr14: 32,086,496-32,086,935 , GRCh37.p13 chr14: 32,555,702-32,556,141 ARHGAP5
    nsv6946829copy number variation1nstd229human GRCh38 chr14: 32,105,968-32,106,628 , GRCh37.p13 chr14: 32,575,174-32,575,834 ARHGAP5
    nsv6943079copy number variation1nstd229human GRCh38 chr14: 32,068,129-32,089,427 , GRCh37.p13 chr14: 32,537,335-32,558,633 ARHGAP5-AS1, ARHGAP5
    nsv6938368copy number variation1nstd229human GRCh38 chr14: 32,156,505-32,325,675 , GRCh37.p13 chr14: 32,625,711-32,794,881 RNU6-7, ARHGAP5, 4 more genes
    nsv6637416copy number variation1nstd102humanPathogenic GRCh37 chr14: 24,959,823-33,415,359 , GRCh38.p12 chr14: 24,490,617-32,946,153 SCFD1, RPL12P5, 94 more genes
    nsv6622516copy number variation2nstd224human GRCh37 chr14: 32,121,501-32,568,311 , GRCh38.p12 chr14: 31,652,295-32,099,105 ARHGAP5, NUBPL, 5 more genes
    nsv6591606inversion1nstd223human GRCh38 chr14: 30,656,873-33,818,146 , GRCh37.p13 chr14: 31,126,079-34,287,352 ARHGAP5-AS1, RN7SL660P, 37 more genes
    nsv6577468inversion1nstd223human GRCh38 chr14: 32,111,911-32,112,605 , GRCh37.p13 chr14: 32,581,117-32,581,811 ARHGAP5
    nsv6492834copy number variation1nstd223human GRCh38 chr14: 32,108,801-32,109,600 , GRCh37.p13 chr14: 32,578,007-32,578,806 ARHGAP5
    nsv6490323copy number variation1nstd223human GRCh38 chr14: 32,085,015-32,085,044 , GRCh37.p13 chr14: 32,554,221-32,554,250 ARHGAP5
    nsv6480955copy number variation1nstd223human GRCh38 chr14: 32,086,496-32,086,931 , GRCh37.p13 chr14: 32,555,702-32,556,137 ARHGAP5
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