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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926397copy number variation1nstd209human GRCh38 chr7: 45,161,872-45,163,913 , GRCh37.p13 chr7: 45,201,471-45,203,512 RAMP3
    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
    nsv5484471copy number variation1nstd206human GRCh38 chr7: 45,166,835-45,166,969 , GRCh37.p13 chr7: 45,206,434-45,206,568 RAMP3
    nsv5475816copy number variation1nstd206human GRCh38 chr7: 45,166,482-45,167,699 , GRCh37.p13 chr7: 45,206,081-45,207,298 RAMP3
    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
    nsv5180145mobile element insertion1nstd203human GRCh38 chr7: 45,183,732-45,183,739 , GRCh37.p13 chr7: 45,223,331-45,223,338 RAMP3
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4956463copy number variation1nstd200human GRCh38 chr7: 45,167,244-45,167,837 , GRCh37.p13 chr7: 45,206,843-45,207,436 RAMP3
    nsv4956462copy number variation1nstd200human GRCh38 chr7: 45,154,703-45,155,875 , GRCh37.p13 chr7: 45,194,302-45,195,474 RAMP3
    nsv4811528copy number variation1nstd200human GRCh37 chr7: 45,206,843-45,207,436 , GRCh38.p12 chr7: 45,167,244-45,167,837 RAMP3
    nsv4811527copy number variation1nstd200human GRCh37 chr7: 45,194,302-45,195,474 , GRCh38.p12 chr7: 45,154,703-45,155,875 RAMP3
    nsv4675126copy number variation1nstd102humanUncertain significance GRCh37 chr7: 44,990,619-45,233,464 , GRCh38.p12 chr7: 44,951,020-45,193,865 CCM2, SNORA5C, 9 more genes
    nsv4605186copy number variation1nstd183human GRCh37 chr7: 45,218,349-45,218,974 , GRCh38.p12 chr7: 45,178,750-45,179,375 RAMP3
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    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
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