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Items: 1 to 20 of 274

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5685102mobile element insertion1nstd211human GRCh38 chr1: 62,857,884-62,857,884 , GRCh37.p13 chr1: 63,323,555-63,323,555 ATG4C
    nsv5685018mobile element insertion1nstd211human GRCh38 chr1: 62,783,707-62,783,707 , GRCh37.p13 chr1: 63,249,378-63,249,378 ATG4C
    nsv5681742mobile element insertion1nstd211human GRCh38 chr1: 62,791,115-62,791,115 , GRCh37.p13 chr1: 63,256,786-63,256,786 ATG4C
    nsv5542566insertion1nstd206human GRCh38 chr1: 62,827,505-62,827,525 , GRCh37.p13 chr1: 63,293,176-63,293,196 ATG4C
    nsv5432437copy number variation1nstd206human GRCh38 chr1: 62,820,846-62,820,904 , GRCh37.p13 chr1: 63,286,517-63,286,575 ATG4C
    nsv5423321copy number variation1nstd206human GRCh38 chr1: 62,797,880-62,804,410 , GRCh37.p13 chr1: 63,263,551-63,270,081 ATG4C
    nsv5422915copy number variation1nstd206human GRCh38 chr1: 62,808,830-62,808,938 , GRCh37.p13 chr1: 63,274,501-63,274,609 ATG4C
    nsv5422567copy number variation1nstd206human GRCh38 chr1: 62,852,408-62,852,482 , GRCh37.p13 chr1: 63,318,079-63,318,153 ATG4C
    nsv5408621mobile element insertion1nstd206human GRCh38 chr1: 62,857,884-62,857,935 , GRCh37.p13 chr1: 63,323,555-63,323,606 ATG4C
    nsv5402384mobile element insertion1nstd206human GRCh38 chr1: 62,791,115-62,791,166 , GRCh37.p13 chr1: 63,256,786-63,256,837 ATG4C
    nsv5352472translocation1nstd200human GRCh38 chr1: 62,852,310-62,852,310 , GRCh38 chr1: 62,850,866-62,850,866 , GRCh37.p13 chr1: 63,316,537-63,316,537 , GRCh37.p13 chr1: 63,317,981-63,317,981 ATG4C
    nsv5342654translocation1nstd200human GRCh37 chr1: 63,247,535-63,247,535 , GRCh37 chr1: 63,247,286-63,247,286 , GRCh38.p12 chr1: 62,781,864-62,781,864 , GRCh38.p12 chr1: 62,781,615-62,781,615 ATG4C
    nsv5334768translocation1nstd200human GRCh37 chr1: 63,252,824-63,252,824 , GRCh37 chr1: 63,247,305-63,247,305 , GRCh38.p12 chr1: 62,787,153-62,787,153 , GRCh38.p12 chr1: 62,781,634-62,781,634 ATG4C
    nsv5281671copy number variation1nstd204human GRCh38.p13 chr1: 62,833,665-62,846,519 , GRCh37.p13 chr1: 63,299,336-63,312,190 ATG4C
    nsv5212554copy number variation1nstd204human GRCh38.p13 chr1: 62,833,053-62,846,576 , GRCh37.p13 chr1: 63,298,724-63,312,247 ATG4C
    nsv5204616copy number variation1nstd204human GRCh38.p13 chr1: 62,861,801-62,868,700 , GRCh37.p13 chr1: 63,327,472-63,334,371 ATG4C
    nsv5202354copy number variation1nstd204human GRCh38.p13 chr1: 62,833,701-62,846,500 , GRCh37.p13 chr1: 63,299,372-63,312,171 ATG4C
    nsv5077168mobile element insertion1nstd203human GRCh38 chr1: 62,792,162-62,792,176 , GRCh37.p13 chr1: 63,257,833-63,257,847 ATG4C
    nsv5073640mobile element insertion1nstd203human GRCh38 chr1: 62,843,765-62,843,779 , GRCh37.p13 chr1: 63,309,436-63,309,450 ATG4C
    nsv4890523copy number variation1nstd200human GRCh38 chr1: 62,842,362-62,853,607 , GRCh37.p13 chr1: 63,308,033-63,319,278 ATG4C
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