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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
    nsv5259437copy number variation1nstd204human GRCh38.p13 chr7: 143,574,501-143,575,100 , GRCh37.p13 chr7: 143,271,594-143,272,193 CTAGE15, RNU6-162P
    nsv5255779copy number variation1nstd204human GRCh38.p13 chr7: 143,572,301-143,574,400 , GRCh37.p13 chr7: 143,269,394-143,271,493 CTAGE15, RNU6-162P
    nsv5253622copy number variation1nstd204human GRCh37.p13 chr7: 143,219,894-143,318,893 , GRCh38.p13 chr7: 143,522,801-143,621,800 EPHA1-AS1, TCAF2, 6 more genes
    nsv5253556copy number variation1nstd204human GRCh38.p13 chr7: 143,550,001-143,574,600 , GRCh37.p13 chr7: 143,247,094-143,271,693 CTAGE15, RNU6-162P
    nsv5250287copy number variation1nstd204human GRCh38.p13 chr7: 143,571,001-143,571,900 , GRCh37.p13 chr7: 143,268,094-143,268,993 CTAGE15
    nsv5244638copy number variation1nstd204human GRCh38.p13 chr7: 143,550,001-143,577,500 , GRCh37.p13 chr7: 143,247,094-143,274,593 CTAGE15, RNU6-162P
    nsv5242196copy number variation1nstd204human GRCh38.p13 chr7: 143,573,301-143,580,300 , GRCh37.p13 chr7: 143,270,394-143,277,393 RNU6-162P, CTAGE15
    nsv5241144copy number variation1nstd204human GRCh38.p13 chr7: 143,574,601-143,585,000 , GRCh37.p13 chr7: 143,271,694-143,282,093 RNU6-162P, CTAGE15
    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
    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
    nsv4663957copy number variation2nstd186human GRCh37 chr7: 143,248,293-143,563,494 , GRCh38.p12 chr7: 143,551,200-143,866,401 , GRCh38.p12 chr7|NW_018654714.1: 170,564-410,625 , RPL26P24, 13 more genes
    nsv4618203copy number variation1nstd183human GRCh37 chr7: 143,257,517-143,339,590 , GRCh38.p12 chr7: 143,560,424-143,642,497 , GRCh38.p12 chr7|NW_018654714.1: 179,788-221,137 TCAF2, CTAGE15, 4 more genes
    nsv4607362copy number variation2nstd183human GRCh37 chr7: 143,248,293-143,563,494 , GRCh38.p12 chr7: 143,551,200-143,866,401 , GRCh38.p12 chr7|NW_018654714.1: 170,564-410,625 , TCAF1, 13 more genes
    nsv4599968copy number variation2nstd183human GRCh37 chr7: 143,216,805-143,557,197 , GRCh38.p12 chr7|NW_018654714.1: 139,076-404,329 , GRCh38.p12 chr7: 143,519,712-143,860,104 , RNU6-267P, 16 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
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