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Items: 1 to 20 of 146

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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
    nsv5490084copy number variation1nstd206human GRCh37.p13 chr7|NW_003571040.1: 414,970-430,966 , GRCh38 chr7: 142,273,000-142,304,990 TRBV1, TRB, 3 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4966904copy number variation1nstd200human GRCh38 chr7: 142,295,817-142,343,436 , GRCh37.p13 chr7: 141,995,657-142,043,266 TRB, TRBV7-1, 7 more genes
    nsv4966903copy number variation1nstd200human GRCh38 chr7: 142,273,000-142,304,990 , GRCh37.p13 chr7|NW_003571040.1: 414,970-430,966 LOC105375539, PRSS3P3, 3 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4684320copy number variation1nstd102humanUncertain significance GRCh37 chr7: 141,937,588-142,486,548 , GRCh38 chr7|NT_187562.1: 199,668-781,128 , NCBI36 chr7: 141,584,062-142,186,550 TRBV6-9, TRBVB, 78 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
    nsv4605394copy number variation1nstd183human GRCh37 chr7: 141,838,718-142,012,291 , GRCh38.p12 chr7: 142,138,918-142,288,986 , GRCh38.p12 chr7|NT_187562.1: 100,798-322,253 TRBV6-2, PRSS3P3, 15 more genes
    nsv4599848copy number variation1nstd183human GRCh37 chr7: 141,947,779-142,480,104 , GRCh38.p12 chr7: 142,288,582-142,732,123 , GRCh38.p12 chr7|NT_187562.1: 209,859-774,850 TRBV6-7, TRBV11-3, 77 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
    nsv4456204copy number variation1nstd102humanUncertain significance GRCh37 chr7: 141,932,561-142,487,154 , GRCh38.p12 chr7: 142,288,582-142,779,344 , GRCh38.p12 chr7|NT_187562.1: 194,641-781,128 TRBVB, TRBV5-3, 80 more genes
    nsv4456043copy number variation1nstd102humanUncertain significance GRCh37 chr7: 141,932,561-142,486,548 , GRCh38.p12 chr7: 142,288,582-142,778,738 , GRCh38.p12 chr7|NT_187562.1: 194,641-781,128 TRBV23-1, LOC105379749, 80 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
    nsv4165710copy number variation1nstd166human GRCh37.p13 chr7: 141,836,318-142,011,033 , GRCh38.p12 chr7: 142,136,518-142,288,986 , GRCh38.p12 chr7|NT_187562.1: 98,398-322,253 MGAM2, MOXD2P, 15 more genes
    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
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