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Items: 1 to 20 of 287

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5878950copy number variation1nstd209human GRCh38 chr1: 211,811,742-211,811,833 , GRCh37.p13 chr1: 211,985,084-211,985,175 LPGAT1
    nsv5874879copy number variation1nstd209human GRCh38 chr1: 211,807,269-211,808,321 , GRCh37.p13 chr1: 211,980,611-211,981,663 LPGAT1
    nsv5871347copy number variation1nstd209human GRCh38 chr1: 211,791,718-211,792,485 , GRCh37.p13 chr1: 211,965,060-211,965,827 RN7SL344P, LPGAT1
    nsv5829186copy number variation1nstd209human GRCh38 chr1: 211,807,229-211,808,609 , GRCh37.p13 chr1: 211,980,571-211,981,951 LPGAT1
    nsv5730803mobile element insertion1nstd211human GRCh38 chr1: 211,779,173-211,779,173 , GRCh37.p13 chr1: 211,952,515-211,952,515 LPGAT1
    nsv5717875mobile element insertion1nstd211human GRCh38 chr1: 211,756,923-211,756,923 , GRCh37.p13 chr1: 211,930,265-211,930,265 LPGAT1
    nsv5568026copy number variation1nstd207human GRCh38 chr1: 211,791,718-211,792,485 , GRCh37.p13 chr1: 211,965,060-211,965,827 RN7SL344P, LPGAT1
    nsv5554694mobile element insertion1nstd206human GRCh38 chr1: 211,779,173-211,779,224 , GRCh37.p13 chr1: 211,952,515-211,952,566 LPGAT1
    nsv5453324copy number variation1nstd206human GRCh38 chr1: 211,807,271-211,808,322 , GRCh37.p13 chr1: 211,980,613-211,981,664 LPGAT1
    nsv5449187copy number variation1nstd206human GRCh38 chr1: 211,770,283-211,770,339 , GRCh37.p13 chr1: 211,943,625-211,943,681 LPGAT1
    nsv5448071copy number variation1nstd206human GRCh38 chr1: 211,790,585-211,790,661 , GRCh37.p13 chr1: 211,963,927-211,964,003 LPGAT1, RN7SL344P
    nsv5446758copy number variation1nstd206human GRCh38 chr1: 211,709,130-211,745,086 , GRCh37.p13 chr1: 211,882,472-211,918,428 LOC105372904, LPGAT1
    nsv5436323copy number variation1nstd206human GRCh38 chr1: 211,791,718-211,792,490 , GRCh37.p13 chr1: 211,965,060-211,965,832 LPGAT1, RN7SL344P
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5354987translocation1nstd200human GRCh38 chr1: 211,808,322-211,808,322 , GRCh38 chr1: 211,807,271-211,807,271 , GRCh37.p13 chr1: 211,981,664-211,981,664 , GRCh37.p13 chr1: 211,980,613-211,980,613 LPGAT1
    nsv5354981translocation1nstd200human GRCh38 chr1: 211,770,339-211,770,339 , GRCh38 chr1: 211,770,283-211,770,283 , GRCh37.p13 chr1: 211,943,681-211,943,681 , GRCh37.p13 chr1: 211,943,625-211,943,625 LPGAT1
    nsv5335424translocation1nstd200human GRCh37 chr1: 211,965,832-211,965,832 , GRCh37 chr1: 211,965,060-211,965,060 , GRCh38.p12 chr1: 211,792,490-211,792,490 , GRCh38.p12 chr1: 211,791,718-211,791,718 RN7SL344P, LPGAT1
    nsv5327724translocation1nstd204human GRCh38.p13 chr1: 211,807,269-211,807,269 , GRCh38.p13 chr1: 211,808,322-211,808,322 , GRCh37.p13 chr1: 211,980,611-211,980,611 , GRCh37.p13 chr1: 211,981,664-211,981,664 LPGAT1
    nsv5299290copy number variation1nstd204human GRCh37.p13 chr1: 211,965,060-211,965,832 , GRCh38.p13 chr1: 211,791,718-211,792,490 LPGAT1, RN7SL344P
    nsv5212234copy number variation1nstd204human GRCh38.p13 chr1: 211,791,801-211,792,500 , GRCh37.p13 chr1: 211,965,143-211,965,842 RN7SL344P, LPGAT1
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