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Items: 1 to 20 of 107

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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
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5183994mobile element insertion1nstd203human GRCh38 chr7: 127,999,780-127,999,794 , GRCh37.p13 chr7: 127,639,833-127,639,847 , SND1, 1 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4958234copy number variation1nstd200human GRCh38 chr7: 127,997,970-128,002,642 , GRCh37.p13 chr7: 127,638,023-127,642,695 , SND1-IT1, 1 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
    nsv4455826copy number variation1nstd102humanPathogenic GRCh37 chr7: 121,480,906-129,389,003 , GRCh38.p12 chr7: 121,840,852-129,749,163 ASB15, PNPT1P2, 127 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
    nsv4322564inversion1nstd166human GRCh37.p13 chr7: 125,283,973-130,824,546 , GRCh38.p12 chr7: 125,643,919-131,139,787 , ARF5, 119 more genes
    nsv4156589copy number variation1nstd166human GRCh37.p13 chr7: 127,504,109-127,681,448 , GRCh38.p12 chr7: 127,864,056-128,041,395 , SND1, 2 more genes
    nsv3923164copy number variation1nstd102humanPathogenic GRCh37 chr7: 121,658,176-128,547,780 , GRCh38 chr7: 122,018,122-128,907,727 , NCBI36 chr7: 121,445,412-128,335,016 GCC1, RNF133, 104 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
    nsv3922595copy number variation1nstd102humanUncertain significance NCBI36 chr7: 127,313,125-127,444,243 , GRCh37.p13 chr7: 127,525,889-127,657,007 , GRCh38.p12 chr7: 127,885,836-128,016,954 SND1, SND1-IT1
    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
    nsv3918979copy number variation1nstd102humanPathogenic GRCh37 chr7: 115,099,069-159,118,507 , NCBI36 chr7: 114,886,305-158,811,268 , GRCh38 chr7: 115,459,015-159,325,817 ABCF2, LOC105375581, 844 more genes
    nsv3917337copy number variation1nstd102humanPathogenic GRCh38 chr7: 121,863,759-159,335,865 , NCBI36 chr7: 121,291,049-158,821,316 , GRCh37 chr7: 121,503,813-159,128,555 INSIG1-DT, RBM33, 776 more genes
    nsv3916726copy number variation1nstd102humanPathogenic NCBI36 chr7: 116,754,095-134,125,980 , GRCh38 chr7: 117,326,805-134,790,689 , GRCh37 chr7: 116,966,859-134,475,440 LOC107986845, TPI1P2, 245 more genes
    nsv3915522copy number variation1nstd102humanPathogenic GRCh38 chr7: 126,859,732-132,750,936 , NCBI36 chr7: 126,287,022-132,086,236 , GRCh37 chr7: 126,499,786-132,435,696 LRRC4, LINC-PINT, 126 more genes
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