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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5542049insertion1nstd206human GRCh38 chr7: 149,255,683-149,255,696 , GRCh37.p13 chr7: 148,952,774-148,952,787 ZNF212
    nsv5380495translocation1nstd200human GRCh38 chr7: 149,239,690-149,239,690 , GRCh38 chr2: 86,914,421-86,914,421 , GRCh37.p13 chr2: 87,141,544-87,141,544 , GRCh37.p13 chr7: 148,936,781-148,936,781 ZNF212, RGPD1
    nsv5371371translocation1nstd200human GRCh38 chr7: 149,254,437-149,254,437 , GRCh38 chr7: 149,254,372-149,254,372 , GRCh37.p13 chr7: 148,951,528-148,951,528 , GRCh37.p13 chr7: 148,951,463-148,951,463 ZNF212
    nsv5119915mobile element insertion1nstd203human GRCh38 chr7: 149,243,433-149,243,481 , GRCh37.p13 chr7: 148,940,524-148,940,572 ZNF212
    nsv5100769mobile element insertion1nstd203human GRCh38 chr7: 149,243,912-149,243,925 , GRCh37.p13 chr7: 148,941,003-148,941,016 ZNF212
    nsv4954060copy number variation1nstd200human GRCh38 chr7: 149,228,570-149,243,467 , GRCh37.p13 chr7: 148,925,661-148,940,558 ZNF212
    nsv4951195copy number variation1nstd200human GRCh38 chr7: 149,244,551-149,246,557 , GRCh37.p13 chr7: 148,941,642-148,943,648 ZNF212
    nsv4812394copy number variation1nstd200human GRCh37 chr7: 148,941,642-148,943,648 , GRCh38.p12 chr7: 149,244,551-149,246,557 ZNF212
    nsv4685723copy number variation1nstd102humannot provided GRCh37 chr7: 147,897,705-149,874,566 , GRCh38.p12 chr7: 148,200,613-150,177,477 CUL1, RNY1, 63 more genes
    nsv4685715copy number variation1nstd102humannot provided GRCh37 chr7: 143,107,740-156,886,246 , GRCh38.p12 chr7: 143,410,647-157,093,552 CTAGE4, CDK5, 277 more genes
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4675615copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620 ATG9B, OR10AC1, 603 more genes
    nsv4675268copy number variation1nstd102humanPathogenic GRCh37 chr7: 145,962,558-159,119,707 , GRCh38.p12 chr7: 146,265,466-159,327,017 ABCB8, THAP5P1, 237 more genes
    nsv4609308copy number variation1nstd183human GRCh37 chr7: 148,927,128-148,936,906 , GRCh38.p12 chr7: 149,230,037-149,239,815 ZNF212
    nsv4455493copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,592,554-159,119,707 , GRCh38.p12 chr7: 130,907,795-159,327,017 OR2A1, LOC101027084, 614 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4452353copy number variation1nstd102humannot provided GRCh37 chr7: 147,897,705-149,874,566 , GRCh38.p12 chr7: 148,200,613-150,177,477 RN7SL569P, ZNF746, 63 more genes
    nsv4381716copy number variation1nstd173human GRCh37 chr7: 146,525,217-159,119,707 , GRCh38.p12 chr7: 146,828,125-159,327,017 , TRC-GCA17-1, 247 more genes
    nsv4349183copy number variation1nstd102humanPathogenic GRCh37 chr7: 128,312,450-159,119,220 , GRCh38.p12 chr7: 128,672,396-159,326,530 LOC105375582, TRBJ2-4, 686 more genes
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