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Items: 1 to 20 of 130

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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
    nsv5181637mobile element insertion1nstd203human GRCh38 chr7: 141,714,885-141,714,901 , GRCh37.p13 chr7: 141,414,685-141,414,701 WEE2, WEE2-AS1
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4968870copy number variation1nstd200human GRCh38 chr7: 141,708,106-141,708,537 , GRCh37.p13 chr7: 141,407,906-141,408,337 WEE2, WEE2-AS1
    nsv4958745copy number variation1nstd200human GRCh38 chr7: 141,714,720-141,719,001 , GRCh37.p13 chr7: 141,414,520-141,418,801 WEE2, WEE2-AS1
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4869975inversion1nstd200human GRCh37 chr7: 140,214,312-141,993,227 , GRCh38.p12 chr7: 140,514,512-142,288,987 , TMEM178B, 44 more genes
    nsv4825392copy number variation1nstd200human GRCh37 chr7: 141,407,906-141,408,337 , GRCh38.p12 chr7|NW_003315922.2: 80,706-81,137 , GRCh38.p12 chr7: 141,708,106-141,708,537 WEE2, WEE2-AS1
    nsv4744860copy number variation1nstd199human GRCh37 chr7: 141,431,516-141,431,587 , GRCh38.p12 chr7: 141,731,716-141,731,787 , GRCh38.p12 chr7|NW_003315922.2: 104,316-104,387 WEE2-AS1, WEE2
    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
    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
    nsv4349183copy number variation1nstd102humanPathogenic GRCh37 chr7: 128,312,450-159,119,220 , GRCh38.p12 chr7: 128,672,396-159,326,530 LOC105375582, TRBJ2-4, 686 more genes
    nsv4156146copy number variation1nstd166human GRCh37.p13 chr7: 141,407,906-141,408,337 , GRCh38.p12 chr7: 141,708,106-141,708,537 , GRCh38.p12 chr7|NW_003315922.2: 80,706-81,137 WEE2, WEE2-AS1
    nsv3964850insertion1nstd168human GRCh38 chr7: 141,667,323-141,724,385 , GRCh37.p13 chr7: 141,367,123-141,424,185 DENND11, WEE2-AS1, 1 more genes
    nsv3930814copy number variation1nstd167human GRCh37 chr7: 141,431,542-141,431,576 , GRCh38.p12 chr7: 141,731,742-141,731,776 , GRCh38.p12 chr7|NW_003315922.2: 104,342-104,376 WEE2-AS1, WEE2
    nsv3924666copy number variation1nstd102humanUncertain significance GRCh38 chr7: 140,061,285-144,622,893 , NCBI36 chr7: 139,407,554-143,950,919 , GRCh37 chr7: 139,761,085-144,319,986 MKRN1, TRBV24-1, 234 more genes
    nsv3924585copy number variation1nstd102humanPathogenic NCBI36 chr7: 130,506,777-158,812,468 , GRCh38 chr7: 131,171,478-159,327,017 , GRCh37 chr7: 130,856,237-159,119,707 PAXBP1P1, RNY3, 611 more genes
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