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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5920861copy number variation1nstd209human GRCh38 chr7: 142,937,288-142,937,442 , GRCh37.p13 chr7: 142,634,385-142,634,539 , LOC105375542
    nsv5914597copy number variation1nstd209human GRCh38 chr7: 142,936,908-142,937,244 , GRCh37.p13 chr7: 142,634,005-142,634,341 , LOC105375542
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5481456copy number variation1nstd206human GRCh38 chr7: 142,937,292-142,937,443 , GRCh37.p13 chr7: 142,634,389-142,634,540 , LOC105375542
    nsv5106414mobile element insertion1nstd203human GRCh38 chr7: 142,936,831-142,936,846 , GRCh37.p13 chr7: 142,633,928-142,633,943 , LOC105375542
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 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
    nsv4616623copy number variation1nstd183human GRCh37 chr7: 142,568,666-142,703,508 , GRCh38.p12 chr7: 142,870,913-143,006,421 , GRCh38.p12 chr7|NT_187562.1: 893,956-1,029,488 , EPHB6, 5 more genes
    nsv4605707copy number variation1nstd183human GRCh37 chr7: 142,568,740-142,707,516 , GRCh38.p12 chr7: 142,870,987-143,010,429 , GRCh38.p12 chr7|NT_187562.1: 894,030-1,033,496 , EPHB6, 5 more genes
    nsv4525104copy number variation1nstd166human GRCh37.p13 chr7: 141,933,998-142,707,100 , GRCh38.p12 chr7: 142,288,582-143,010,013 , GRCh38.p12 chr7|NT_187562.1: 196,078-914,081 , TRBJ2-6, 108 more genes
    nsv4457314copy number variation1nstd102humanUncertain significance GRCh37 chr7: 141,751,875-147,105,208 , GRCh38.p12 chr7: 142,052,075-147,408,116 ARHGEF5, FAM131B-AS2, 195 more genes
    nsv4456696copy number variation1nstd102humanUncertain significance GRCh37 chr7: 142,565,890-142,706,787 , GRCh38.p12 chr7|NT_187562.1: 891,178-1,032,767 , GRCh38.p12 chr7: 142,868,135-143,009,700 EPHB6, KEL, 4 more genes
    nsv4456689copy number variation1nstd102humanUncertain significance GRCh37 chr7: 142,568,958-142,706,787 , GRCh38.p12 chr7: 142,871,205-143,009,700 , GRCh38.p12 chr7|NT_187562.1: 894,247-1,032,767 EPHB6, KEL, 4 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
    nsv4327487inversion1nstd166human GRCh37.p13 chr7: 142,583,556-142,801,968 , GRCh38.p12 chr7: 142,885,811-143,104,875 , GRCh38.p12 chr7|NT_187562.1: 908,851-1,111,570 , TRPV6, 9 more genes
    nsv4157824copy number variation1nstd166human GRCh37.p13 chr7: 142,634,389-142,634,540 , GRCh38.p12 chr7: 142,937,292-142,937,443 , GRCh38.p12 chr7|NT_187562.1: 960,359-960,510 , LOC105375542
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