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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5722589mobile element insertion2nstd211human GRCh38 chr7: 44,799,072-44,799,072 , GRCh37.p13 chr7: 44,838,671-44,838,671 PPIA
    nsv5556950sequence alteration1nstd206human GRCh38 chr7: 44,712,903-47,388,095 , GRCh37.p13 chr7: 44,752,502-47,427,692 , ADCY1, 51 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5491322copy number variation1nstd206human GRCh38 chr7: 44,802,945-44,803,203 , GRCh37.p13 chr7: 44,842,544-44,842,802 PPIA
    nsv5381787copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,341,583-50,171,623 , GRCh38.p12 chr7: 43,301,984-50,132,027 OGDH, LOC112267918, 110 more genes
    nsv5381783copy number variation1nstd102humanPathogenic GRCh37 chr7: 41,124,364-47,945,566 , GRCh38.p12 chr7: 41,084,766-47,905,969 ELK1P1, URGCP, 121 more genes
    nsv5224790copy number variation1nstd204human GRCh38.p13 chr7: 44,789,601-44,835,100 , GRCh37.p13 chr7: 44,829,200-44,874,699 , LOC105375259, 2 more genes
    nsv5221233copy number variation1nstd204human GRCh38.p13 chr7: 44,597,101-45,000,100 , GRCh37.p13 chr7: 44,636,700-45,039,699 , PPIA, 14 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 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
    nsv4369952copy number variation1nstd173human GRCh37 chr7: 44,814,172-44,840,028 , GRCh38.p12 chr7: 44,774,573-44,800,429 LOC105375259, PPIA
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv4137351copy number variation1nstd166human GRCh37.p13 chr7: 44,827,470-44,834,435 , GRCh38.p12 chr7: 44,787,871-44,794,836 LOC105375259, PPIA
    nsv3924742copy number variation1nstd102humanPathogenic GRCh37 chr7: 38,217,601-45,343,699 , GRCh38 chr7: 38,177,999-45,304,100 , NCBI36 chr7: 38,184,126-45,310,224 NUDCD3, KRT8P20, 152 more genes
    nsv3924054copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,573,756-56,174,815 , NCBI36 chr7: 40,540,281-56,142,309 , GRCh38 chr7: 40,534,157-56,107,122 VOPP1-DT, SGO1P2, 229 more genes
    nsv3920348copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,232,968-46,597,979 , GRCh38 chr7: 44,193,369-46,558,381 , NCBI36 chr7: 44,199,493-46,564,504 CCM2, ADCY1, 50 more genes
    nsv3919937copy number variation1nstd102humanPathogenic GRCh38 chr7: 44,571,949-53,699,760 , GRCh37 chr7: 44,611,548-53,767,453 , NCBI36 chr7: 44,578,073-53,734,947 LOC105375262, LOC105375259, 106 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
    nsv3919299copy number variation1nstd102humanUncertain significance GRCh37 chr7: 44,385,397-45,116,068 , NCBI36 chr7: 44,351,922-45,082,593 , GRCh38 chr7: 44,345,798-45,076,469 RNU6-1097P, SNORA9, 20 more genes
    nsv3918948copy number variation1nstd102humanPathogenic GRCh37 chr7: 39,103,000-45,402,695 , GRCh38 chr7: 39,063,400-45,363,096 , NCBI36 chr7: 39,069,525-45,369,220 MRPS23P1, CDK13, 120 more genes
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