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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5914480copy number variation1nstd209human GRCh38 chr7: 143,394,019-143,394,869 , GRCh37.p13 chr7: 143,091,112-143,091,962 EPHA1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4968892copy number variation1nstd200human GRCh38 chr7: 143,403,512-143,403,670 , GRCh37.p13 chr7: 143,100,605-143,100,763 EPHA1
    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
    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
    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
    nsv4368220copy number variation1nstd173human GRCh37 chr7: 143,082,657-143,430,204 , GRCh38.p12 chr7: 143,385,564-143,733,111 , GRCh38.p12 chr7|NW_018654714.1: 4,928-277,430 , OR2R1P, 16 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
    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
    nsv3922815copy number variation1nstd102humanPathogenic NCBI36 chr7: 96,887,100-158,409,214 , GRCh38 chr7: 97,419,852-158,923,762 , GRCh37 chr7: 97,049,164-158,716,453 SEPTIN7P6, MIR93, 1175 more genes
    nsv3922224copy number variation1nstd102humanPathogenic GRCh38 chr7: 141,126,407-145,652,221 , GRCh37 chr7: 140,826,207-145,349,314 , NCBI36 chr7: 140,472,676-144,980,247 CTAGE4, TRBD1, 212 more genes
    nsv3920625copy number variation1nstd102humanPathogenic GRCh38 chr7: 142,578,948-144,254,897 , NCBI36 chr7: 141,967,554-143,582,923 , GRCh37 chr7: 142,528,609-143,951,990 OR2A14, TAS2R41, 120 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
    nsv3919772copy number variation1nstd102humanPathogenic NCBI36 chr7: 141,307,130-158,821,317 , GRCh37 chr7: 142,528,609-159,128,556 , GRCh38 chr7: 141,960,861-159,335,866 LOC105375567, LOC389602, 429 more genes
    nsv3919545copy number variation1nstd102humanPathogenic NCBI36 chr7: 130,564,063-158,821,317 , GRCh37 chr7: 130,913,523-159,128,556 , GRCh38 chr7: 131,228,764-159,335,866 LOC105375594, CLCN1, 611 more genes
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