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Items: 1 to 20 of 210

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5936848copy number variation1nstd209human GRCh38 chr17: 75,113,037-75,113,365 , GRCh37.p13 chr17: 73,109,132-73,109,460 ARMC7
    nsv5934561copy number variation1nstd209human GRCh38 chr17: 75,111,633-75,112,142 , GRCh37.p13 chr17: 73,107,728-73,108,237 ARMC7
    nsv5591663copy number variation1nstd207human GRCh38 chr17: 75,111,633-75,112,142 , GRCh37.p13 chr17: 73,107,728-73,108,237 ARMC7
    nsv5533137copy number variation1nstd206human GRCh38 chr17: 75,107,785-75,120,664 , GRCh37.p13 chr17: 73,103,880-73,116,759 ARMC7
    nsv5532235copy number variation1nstd206human GRCh38 chr17: 75,121,529-75,123,826 , GRCh37.p13 chr17: 73,117,624-73,119,921 ARMC7
    nsv5520537copy number variation1nstd206human GRCh38 chr17: 75,108,715-75,108,994 , GRCh37.p13 chr17: 73,104,810-73,105,089 ARMC7
    nsv5519854copy number variation1nstd206human GRCh38 chr17: 75,111,651-75,112,143 , GRCh37.p13 chr17: 73,107,746-73,108,238 ARMC7
    nsv5391910copy number variation2nstd186human GRCh37 chr17: 73,107,746-73,108,238 , GRCh38.p12 chr17: 75,111,651-75,112,143 ARMC7
    nsv5380189translocation1nstd200human GRCh38 chr16: 30,165,227-30,165,227 , GRCh38 chr17: 75,108,957-75,108,957 , GRCh37.p13 chr16: 30,176,548-30,176,548 , GRCh37.p13 chr17: 73,105,052-73,105,052 ARMC7
    nsv5377665translocation1nstd200human GRCh38 chr17: 75,130,664-75,130,664 , GRCh38 chr4: 143,217,245-143,217,245 , GRCh37.p13 chr17: 73,126,759-73,126,759 , GRCh37.p13 chr4: 144,138,398-144,138,398 NT5C, ARMC7, 2 more genes
    nsv5339799translocation1nstd200human GRCh37 chr16: 30,176,548-30,176,548 , GRCh37 chr17: 73,105,052-73,105,052 , GRCh38.p12 chr17: 75,108,957-75,108,957 , GRCh38.p12 chr16: 30,165,227-30,165,227 ARMC7
    nsv5329464copy number variation1nstd204human GRCh38.p13 chr17: 75,111,641-75,112,147 , GRCh37.p13 chr17: 73,107,736-73,108,242 ARMC7
    nsv5298973copy number variation1nstd204human GRCh38.p13 chr17: 74,951,501-75,212,200 , GRCh37.p13 chr17: 72,947,596-73,208,295 RNU6-362P, TRR-CCT2-1, 17 more genes
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
    nsv5151750mobile element insertion1nstd203human GRCh38 chr17: 75,111,139-75,111,172 , GRCh37.p13 chr17: 73,107,234-73,107,267 ARMC7
    nsv5146737mobile element insertion1nstd203human GRCh38 chr17: 75,123,911-75,123,928 , GRCh37.p13 chr17: 73,120,006-73,120,023 ARMC7
    nsv5142608mobile element insertion1nstd203human GRCh38 chr17: 75,123,917-75,123,928 , GRCh37.p13 chr17: 73,120,012-73,120,023 ARMC7
    nsv5029562inversion1nstd200human GRCh38 chr17: 64,441,870-75,217,767 , GRCh37.p13 chr17: 62,649,312-73,213,862 , LOC102929163, 207 more genes
    nsv5016661copy number variation1nstd200human GRCh38 chr17: 75,118,290-75,122,781 , GRCh37.p13 chr17: 73,114,385-73,118,876 ARMC7
    nsv5016660copy number variation1nstd200human GRCh38 chr17: 75,111,651-75,112,143 , GRCh37.p13 chr17: 73,107,746-73,108,238 ARMC7
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