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Items: 1 to 20 of 213

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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
    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
    nsv4685715copy number variation1nstd102humannot provided GRCh37 chr7: 143,107,740-156,886,246 , GRCh38.p12 chr7: 143,410,647-157,093,552 CTAGE4, CDK5, 277 more genes
    nsv4679160copy number variation1nstd189human GRCh37.p13 chr7: 143,421,819-143,974,156 , GRCh38.p12 chr7: 143,724,726-144,277,063 , GRCh38.p12 chr7|NW_018654714.1: 269,045-589,656 , TCAF1, 36 more genes
    nsv4679008copy number variation1nstd189human GRCh37.p13 chr7: 143,226,900-143,917,601 , GRCh38.p12 chr7: 143,529,807-144,220,508 , GRCh38.p12 chr7|NW_018654714.1: 149,171-589,656 , TCAF1, 37 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
    nsv4604997copy number variation1nstd183human GRCh37 chr7: 143,439,646-144,064,358 , GRCh38.p12 chr7: 143,742,553-144,367,265 , GRCh38.p12 chr7|NW_018654715.1: 1-403,724 , TCAF1, 43 more genes
    nsv4599315copy number variation1nstd183human GRCh37 chr7: 143,265,141-143,925,046 , GRCh38.p12 chr7|NW_018654714.1: 187,412-589,656 , GRCh38.p12 chr7: 143,568,048-144,227,953 , CTAGE4, 35 more genes
    nsv4524056copy number variation1nstd166human GRCh37.p13 chr7: 143,526,997-143,878,000 , GRCh38.p12 chr7: 143,829,904-144,180,907 , GRCh38.p12 chr7|NW_018654714.1: 374,203-589,656 TCAF1, OR2A14, 19 more genes
    nsv4457358copy number variation1nstd102humanUncertain significance GRCh37 chr7: 143,572,320-144,474,990 , GRCh38.p12 chr7: 143,875,227-144,777,897 , GRCh38.p12 chr7|NW_018654715.1: 1-680,662 LOC112268383, OR2A3P, 38 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
    nsv4402958copy number variation1nstd174human GRCh37 chr7: 143,425,378-144,073,953 , GRCh38.p12 chr7: 143,728,285-144,376,860 , GRCh38.p12 chr7|NW_018654715.1: 1-409,704 , ARHGEF5, 44 more genes
    nsv4372779copy number variation1nstd173human GRCh37 chr7: 143,425,719-143,873,939 , GRCh38.p12 chr7: 143,728,626-144,176,846 , GRCh38.p12 chr7|NW_018654714.1: 272,945-589,656 CTAGE6, OR2F2, 25 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
    nsv4342554sequence alteration1nstd166human GRCh37.p13 chr7: 143,761,186-143,828,428 , GRCh38.p12 chr7: 144,064,093-144,131,335 , GRCh38.p12 chr7|NW_018654715.1: 18,665-85,889 OR2A14, OR2A15P, 5 more genes
    nsv4159829copy number variation1nstd166human GRCh37.p13 chr7: 143,513,900-143,879,500 , GRCh38.p12 chr7|NW_018654714.1: 361,109-589,656 , GRCh38.p12 chr7: 143,816,807-144,182,407 OR6B1, LOC112267988, 20 more genes
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