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Items: 1 to 20 of 502

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960677insertion1nstd209human GRCh38 chr2: 200,468,347-200,468,347 , GRCh37.p13 chr2: 201,333,070-201,333,070 SPATS2L, LOC101927741
    nsv5948194insertion1nstd209human GRCh38 chr2: 200,330,214-200,330,214 , GRCh37.p13 chr2: 201,194,937-201,194,937 SPATS2L
    nsv5898204copy number variation1nstd209human GRCh38 chr2: 200,366,123-200,366,579 , GRCh37.p13 chr2: 201,230,846-201,231,302 SPATS2L
    nsv5686247mobile element insertion1nstd211human GRCh38 chr2: 200,443,132-200,443,132 , GRCh37.p13 chr2: 201,307,855-201,307,855 LOC101927741, SPATS2L
    nsv5684113mobile element insertion1nstd211human GRCh38 chr2: 200,346,870-200,346,870 , GRCh37.p13 chr2: 201,211,593-201,211,593 SPATS2L
    nsv5680201mobile element insertion1nstd211human GRCh38 chr2: 200,424,060-200,424,060 , GRCh37.p13 chr2: 201,288,783-201,288,783 , SPATS2L
    nsv5679724mobile element insertion2nstd211human GRCh38 chr2: 200,438,728-200,438,728 , GRCh37.p13 chr2: 201,303,451-201,303,451 LOC101927741, SPATS2L
    nsv5620420insertion1nstd207human GRCh38 chr2: 200,330,213-200,330,213 , GRCh37.p13 chr2: 201,194,936-201,194,936 SPATS2L
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5549899insertion1nstd206human GRCh38 chr2: 200,330,213-200,330,213 , GRCh37.p13 chr2: 201,194,936-201,194,936 SPATS2L
    nsv5453374copy number variation1nstd206human GRCh38 chr2: 200,407,086-200,407,226 , GRCh37.p13 chr2: 201,271,809-201,271,949 SPATS2L
    nsv5447718copy number variation1nstd206human GRCh38 chr2: 200,420,300-200,420,379 , GRCh37.p13 chr2: 201,285,023-201,285,102 , SPATS2L
    nsv5447041copy number variation1nstd206human GRCh38 chr2: 200,458,053-200,458,254 , GRCh37.p13 chr2: 201,322,776-201,322,977 LOC101927741, SPATS2L
    nsv5445548copy number variation1nstd206human GRCh38 chr2: 200,356,790-200,356,952 , GRCh37.p13 chr2: 201,221,513-201,221,675 SPATS2L
    nsv5442662copy number variation1nstd206human GRCh38 chr2: 200,332,406-200,335,862 , GRCh37.p13 chr2: 201,197,129-201,200,585 SPATS2L
    nsv5442543copy number variation1nstd206human GRCh38 chr2: 200,369,988-200,372,490 , GRCh37.p13 chr2: 201,234,711-201,237,213 SPATS2L, RNY4P34
    nsv5441361copy number variation1nstd206human GRCh38 chr2: 200,384,553-200,385,894 , GRCh37.p13 chr2: 201,249,276-201,250,617 SPATS2L
    nsv5412005mobile element insertion1nstd206human GRCh38 chr2: 200,424,060-200,424,111 , GRCh37.p13 chr2: 201,288,783-201,288,834 , SPATS2L
    nsv5409404mobile element insertion1nstd206human GRCh38 chr2: 200,438,728-200,438,779 , GRCh37.p13 chr2: 201,303,451-201,303,502 LOC101927741, SPATS2L
    nsv5408225mobile element insertion1nstd206human GRCh38 chr2: 200,346,870-200,346,921 , GRCh37.p13 chr2: 201,211,593-201,211,644 SPATS2L
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