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Items: 1 to 20 of 286

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5721097mobile element insertion1nstd211human GRCh38 chr1: 157,021,798-157,021,798 , GRCh37.p13 chr1: 156,991,590-156,991,590 ARHGEF11
    nsv5690704mobile element insertion1nstd211human GRCh38 chr1: 157,041,701-157,041,701 , GRCh37.p13 chr1: 157,011,493-157,011,493 ARHGEF11
    nsv5569815copy number variation1nstd207human GRCh38 chr1: 157,035,871-157,035,938 , GRCh37.p13 chr1: 157,005,663-157,005,730 ARHGEF11
    nsv5559217mobile element insertion1nstd206human GRCh38 chr1: 157,021,798-157,021,849 , GRCh37.p13 chr1: 156,991,590-156,991,641 ARHGEF11
    nsv5424209copy number variation1nstd206human GRCh38 chr1: 157,030,184-157,030,259 , GRCh37.p13 chr1: 156,999,976-157,000,051 ARHGEF11
    nsv5419157copy number variation1nstd206human GRCh38 chr1: 157,034,217-157,043,675 , GRCh37.p13 chr1: 157,004,009-157,013,467 ARHGEF11
    nsv5403120mobile element insertion1nstd206human GRCh38 chr1: 157,041,701-157,041,752 , GRCh37.p13 chr1: 157,011,493-157,011,544 ARHGEF11
    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
    nsv5335341translocation1nstd200human GRCh37 chr1: 157,015,550-157,015,550 , GRCh37 chr1: 157,015,464-157,015,464 , GRCh38.p12 chr1: 157,045,672-157,045,672 , GRCh38.p12 chr1: 157,045,758-157,045,758 ARHGEF11
    nsv5079930mobile element insertion1nstd203human GRCh38 chr1: 156,949,446-156,949,459 , GRCh37.p13 chr1: 156,919,238-156,919,251 ARHGEF11
    nsv5063830mobile element insertion1nstd203human GRCh38 chr1: 156,991,734-156,991,780 , GRCh37.p13 chr1: 156,961,526-156,961,572 ARHGEF11
    nsv4897612copy number variation1nstd200human GRCh38 chr1: 157,029,748-157,029,906 , GRCh37.p13 chr1: 156,999,540-156,999,698 ARHGEF11
    nsv4897611copy number variation1nstd200human GRCh38 chr1: 157,027,955-157,033,901 , GRCh37.p13 chr1: 156,997,747-157,003,693 ARHGEF11
    nsv4784356copy number variation1nstd200human GRCh37 chr1: 157,007,129-157,014,032 , GRCh38.p12 chr1: 157,037,337-157,044,240 ARHGEF11
    nsv4784355copy number variation1nstd200human GRCh37 chr1: 156,999,540-156,999,698 , GRCh38.p12 chr1: 157,029,748-157,029,906 ARHGEF11
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4736822copy number variation1nstd199human GRCh37 chr1: 157,005,609-157,005,672 , GRCh38.p12 chr1: 157,035,817-157,035,880 ARHGEF11
    nsv4535623insertion1nstd166human GRCh37.p13 chr1: 156,992,304-156,992,304 , GRCh38.p12 chr1: 157,022,512-157,022,512 ARHGEF11
    nsv4327204inversion1nstd166human GRCh37.p13 chr1: 156,223,026-186,411,081 , GRCh38.p12 chr1: 156,253,235-186,441,949 , FASLG, 707 more genes
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