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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3885254copy number variation1nstd102humanBenign GRCh37 chr2: 238,549,369-238,559,307 , GRCh38.p12 chr2: 237,640,726-237,650,664 LRRFIP1
    nsv3871299copy number variation1nstd102humanBenign GRCh37 chr2: 238,554,034-238,559,117 , GRCh38.p12 chr2: 237,645,391-237,650,474 LRRFIP1
    nsv3886037copy number variation1nstd102humanBenign GRCh37 chr2: 238,597,790-238,607,791 , GRCh38.p12 chr2: 237,689,147-237,699,148 LRRFIP1
    nsv3881783copy number variation1nstd102humanBenign GRCh37 chr2: 238,597,790-238,603,174 , GRCh38.p12 chr2: 237,689,147-237,694,531 LRRFIP1
    nsv3887795copy number variation1nstd102humanBenign GRCh37 chr2: 238,597,790-238,601,062 , GRCh38.p12 chr2: 237,689,147-237,692,419 LRRFIP1
    nsv3872117copy number variation1nstd102humanBenign GRCh37 chr2: 238,597,790-238,600,812 , GRCh38.p12 chr2: 237,689,147-237,692,169 LRRFIP1
    nsv3871881copy number variation2nstd102humanBenign GRCh37 chr2: 238,600,028-238,601,062 , GRCh38.p12 chr2: 237,691,385-237,692,419 LRRFIP1
    nsv3871042copy number variation1nstd102humanBenign GRCh37 chr2: 238,600,138-238,601,062 , GRCh38.p12 chr2: 237,691,495-237,692,419 LRRFIP1
    nsv3874514copy number variation1nstd102humanBenign GRCh37 chr2: 238,600,516-238,600,812 , GRCh38.p12 chr2: 237,691,873-237,692,169 LRRFIP1
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 LRRFIP1, DAZAP2P1, 2991 more genes
    nsv6313668copy number variation1nstd102humanPathogenic GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062 LRRFIP1, LOC105373947, 357 more genes
    nsv3898929copy number variation2nstd102humanPathogenic GRCh38 chr2: 231,770,279-242,126,245 , GRCh37 chr2: 232,634,989-243,059,659 , NCBI36 chr2: 232,343,233-242,717,069 LRRFIP1, PDE6D, 227 more genes
    nsv4768328copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,110,452-243,028,452 , GRCh38.p12 chr2: 232,245,742-242,086,301 LRRFIP1, LOC107985836, 217 more genes
    nsv6315436copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,227,837-242,783,384 , GRCh38.p12 chr2: 232,363,127-241,841,232 LRRFIP1, LOC105373929, 204 more genes
    nsv3871027copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,784,243-243,040,217 , GRCh38.p12 chr2: 232,919,533-242,098,066 LRRFIP1, MROH2A, 194 more genes
    nsv3910501copy number variation1nstd102humanPathogenic NCBI36 chr2: 233,599,457-242,717,007 , GRCh37.p13 chr2: 233,891,213-243,068,334 , GRCh38.p12 chr2: 233,026,503-242,126,183 LRRFIP1, UGT1A3, 194 more genes
    nsv3894767copy number variation1nstd102humanPathogenic GRCh38 chr2: 233,420,162-242,086,301 , NCBI36 chr2: 233,704,084-242,677,125 , GRCh37 chr2: 233,995,840-243,028,452 LRRFIP1, LOC112268433, 184 more genes
    nsv3892808copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,362,257-243,041,306 , NCBI36 chr2: 234,026,996-242,689,979 , GRCh38 chr2: 233,453,611-242,099,155 LRRFIP1, RPL3P5, 185 more genes
    nsv3877071copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,495,262-242,783,384 , GRCh38.p12 chr2: 233,586,616-241,841,232 LRRFIP1, RNU6-1140P, 171 more genes
    nsv4674624copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,791,927-242,783,384 , GRCh38.p12 chr2: 233,883,281-241,841,232 LRRFIP1, LOC93463, 151 more genes
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