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Items: 1 to 20 of 322

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147622insertion1nstd232human GRCh37.p13 chr2: 665,622-665,622 , GRCh38.p12 chr2: 665,622-665,622 TMEM18
    nsv7050449inversion1nstd229human GRCh38 chr2: 626,281-1,037,968 , GRCh37.p13 chr2: 626,281-1,033,654 TMEM18-DT, LOC105373479, 7 more genes
    nsv7045635inversion1nstd229human GRCh38 chr2: 660,871-665,238 , GRCh37.p13 chr2: 660,871-665,238 TMEM18
    nsv7039393inversion1nstd229human GRCh38 chr2: 378,067-4,298,462 , GRCh37.p13 chr2: 378,067-4,346,052 LOC105373393, RPS7, 42 more genes
    nsv6674644copy number variation1nstd229human GRCh38 chr2: 424,829-956,456 , GRCh37.p13 chr2: 424,829-952,142 LINC01874, LOC105373480, 11 more genes
    nsv6673660copy number variation1nstd229human GRCh38 chr2: 386,148-840,897 , GRCh37.p13 chr2: 386,148-836,838 LOC105373479, TMEM18-DT, 9 more genes
    nsv6673504copy number variation1nstd229human GRCh38 chr2: 522,694-663,255 , GRCh37.p13 chr2: 522,694-663,255 LINC01875, LOC105373352, 1 more genes
    nsv6672927copy number variation1nstd229human GRCh38 chr2: 346,311-815,761 , GRCh37.p13 chr2: 346,311-811,634 LOC105373351, LINC01875, 9 more genes
    nsv6672611copy number variation1nstd229human GRCh38 chr2: 384,632-967,171 , GRCh37.p13 chr2: 384,632-962,857 LINC01939, SNTG2-AS1, 12 more genes
    nsv6672178copy number variation1nstd229human GRCh38 chr2: 325,900-1,026,860 , GRCh37.p13 chr2: 325,900-1,022,546 LOC105373358, SNTG2, 13 more genes
    nsv6670283copy number variation1nstd229human GRCh38 chr2: 467,239-714,992 , GRCh37.p13 chr2: 467,239-714,992 LOC105373352, TMEM18, 6 more genes
    nsv6669044copy number variation1nstd229human GRCh38 chr2: 438,242-954,089 , GRCh37.p13 chr2: 438,242-949,775 TMEM18, LOC100996637, 11 more genes
    nsv6668795copy number variation1nstd229human GRCh38 chr2: 659,101-666,400 , GRCh37.p13 chr2: 659,101-666,400 TMEM18
    nsv6667959copy number variation1nstd229human GRCh38 chr2: 592,865-815,477 , GRCh37.p13 chr2: 592,865-811,350 TMEM18, LOC105373358, 4 more genes
    nsv6666437copy number variation1nstd229human GRCh38 chr2: 658,635-667,364 , GRCh37.p13 chr2: 658,635-667,364 TMEM18
    nsv6666230copy number variation1nstd229human GRCh38 chr2: 555,557-811,748 , GRCh37.p13 chr2: 555,557-809,338 LOC105373479, LINC01115, 5 more genes
    nsv6665555copy number variation1nstd229human GRCh38 chr2: 670,166-1,126,020 , GRCh37.p13 chr2: 670,166-1,121,706 SNTG2-AS1, TMEM18-DT, 7 more genes
    nsv6665144copy number variation1nstd229human GRCh38 chr2: 483,286-1,041,624 , GRCh37.p13 chr2: 483,286-1,037,310 LINC01939, SNTG2-AS1, 11 more genes
    nsv6661500copy number variation1nstd229human GRCh38 chr2: 548,753-1,162,338 , GRCh37.p13 chr2: 548,753-1,158,024 LOC105373480, SNTG2-AS1, 8 more genes
    nsv6660414copy number variation1nstd229human GRCh38 chr2: 666,993-668,248 , GRCh37.p13 chr2: 666,993-668,248 TMEM18
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