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Items: 1 to 20 of 127

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5915729copy number variation1nstd209human GRCh38 chr7: 122,295,050-122,299,532 , GRCh37.p13 chr7: 121,935,104-121,939,586 FEZF1
    nsv5855310copy number variation1nstd209human GRCh38 chr7: 122,295,067-122,299,546 , GRCh37.p13 chr7: 121,935,121-121,939,600 FEZF1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5482451copy number variation1nstd206human GRCh38 chr7: 122,307,904-122,308,348 , GRCh37.p13 chr7: 121,947,958-121,948,402 FEZF1, FEZF1-AS1
    nsv5381759copy number variation1nstd102humanPathogenic GRCh37 chr7: 116,297,277-126,370,694 , GRCh38.p12 chr7: 116,657,223-126,730,640 TMEM229A, ST7-OT3, 110 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
    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
    nsv4958010copy number variation1nstd200human GRCh38 chr7: 122,295,050-122,299,533 , GRCh37.p13 chr7: 121,935,104-121,939,587 FEZF1
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4820356copy number variation1nstd200human GRCh37 chr7: 121,947,958-121,948,402 , GRCh38.p12 chr7: 122,307,904-122,308,348 FEZF1-AS1, FEZF1
    nsv4820355copy number variation1nstd200human GRCh37 chr7: 121,935,104-121,939,587 , GRCh38.p12 chr7: 122,295,050-122,299,533 FEZF1
    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
    nsv4675322copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,617,406-123,217,914 , GRCh38.p12 chr7: 106,976,961-123,577,860 CBLL1-AS1, COMETT, 168 more genes
    nsv4524910copy number variation1nstd166human GRCh37.p13 chr7: 121,947,958-121,948,402 , GRCh38.p12 chr7: 122,307,904-122,308,348 FEZF1, FEZF1-AS1
    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
    nsv4170202copy number variation1nstd166human GRCh37.p13 chr7: 121,935,104-121,939,587 , GRCh38.p12 chr7: 122,295,050-122,299,533 FEZF1
    nsv3923570copy number variation1nstd102humanPathogenic NCBI36 chr7: 107,583,881-122,963,817 , GRCh37.p13 chr7: 107,796,645-123,176,581 , GRCh38.p12 chr7: 108,156,200-123,536,527 ANKRD7, NDUFA5, 142 more genes
    nsv3923381copy number variation1nstd102humanUncertain significance GRCh37 chr7: 121,101,368-122,522,849 , NCBI36 chr7: 120,888,604-122,310,085 , GRCh38 chr7: 121,461,314-122,882,795 LOC105375481, LOC102724527, 15 more genes
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