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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5115930mobile element insertion1nstd203human GRCh38 chr7: 139,019,578-139,019,587 , GRCh37.p13 chr7: 138,704,324-138,704,333 ZC3HAV1L
    nsv5109451mobile element insertion1nstd203human GRCh38 chr7: 139,019,576-139,019,587 , GRCh37.p13 chr7: 138,704,322-138,704,333 ZC3HAV1L
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4968834copy number variation1nstd200human GRCh38 chr7: 139,020,445-139,083,760 , GRCh37.p13 chr7: 138,705,191-138,768,506 ZC3HAV1, RPL17P28, 3 more genes
    nsv4958639copy number variation1nstd200human GRCh38 chr7: 139,036,645-139,038,490 , GRCh37.p13 chr7: 138,721,391-138,723,236 ZC3HAV1L, LOC107986852
    nsv4958638copy number variation1nstd200human GRCh38 chr7: 139,035,250-139,037,395 , GRCh37.p13 chr7: 138,719,996-138,722,141 ZC3HAV1L, LOC107986852
    nsv4958637copy number variation1nstd200human GRCh38 chr7: 139,032,603-139,032,831 , GRCh37.p13 chr7: 138,717,349-138,717,577 ZC3HAV1L
    nsv4958636copy number variation1nstd200human GRCh38 chr7: 139,017,675-139,032,514 , GRCh37.p13 chr7: 138,702,421-138,717,260 ZC3HAV1L
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4827151copy number variation1nstd200human GRCh37 chr7: 138,717,349-138,717,577 , GRCh38.p12 chr7: 139,032,603-139,032,831 ZC3HAV1L
    nsv4676044copy number variation1nstd102humanPathogenic GRCh37 chr7: 135,677,938-139,810,886 , GRCh38.p12 chr7: 135,993,190-140,111,086 SVOPL, RPS17P12, 62 more genes
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4675615copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620 ATG9B, OR10AC1, 603 more genes
    nsv4612411copy number variation1nstd183human GRCh37 chr7: 138,720,388-138,720,867 , GRCh38.p12 chr7: 139,035,642-139,036,121 LOC107986852, ZC3HAV1L
    nsv4457201copy number variation1nstd102humanUncertain significance GRCh37 chr7: 137,675,423-139,084,024 , GRCh38.p12 chr7: 137,990,677-139,399,278 ZC3HAV1L, TRR-CCT4-1, 34 more genes
    nsv4456915copy number variation1nstd102humanUncertain significance GRCh37 chr7: 137,848,980-138,897,699 , GRCh38.p12 chr7: 138,164,234-139,212,953 ATP6V0A4, KIAA1549, 20 more genes
    nsv4455493copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,592,554-159,119,707 , GRCh38.p12 chr7: 130,907,795-159,327,017 OR2A1, LOC101027084, 614 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
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