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Items: 1 to 20 of 325

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970490inversion1nstd209human GRCh38 chr2: 240,811,836-241,011,847 , GRCh37.p13 chr2: 241,751,253-241,951,264 AGXT, KIF1A, 7 more genes
    nsv5615846insertion1nstd207human GRCh38 chr2: 241,015,720-241,015,720 , GRCh37.p13 chr2: 241,955,137-241,955,137 SNED1-AS1, SNED1
    nsv5605740insertion1nstd207human GRCh38 chr2: 241,016,047-241,016,047 , GRCh37.p13 chr2: 241,955,464-241,955,464 SNED1, SNED1-AS1
    nsv5381323copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,201,756-243,048,760 , GRCh38.p12 chr2: 236,293,113-242,106,609 LRRFIP1, GPR35, 133 more genes
    nsv5351293translocation1nstd200human GRCh38 chr2: 241,013,943-241,013,943 , GRCh38 chr2: 241,013,844-241,013,844 , GRCh37.p13 chr2: 241,953,261-241,953,261 , GRCh37.p13 chr2: 241,953,360-241,953,360 SNED1-AS1, SNED1
    nsv5343475translocation1nstd200human GRCh37 chr2: 241,953,360-241,953,360 , GRCh37 chr2: 241,953,261-241,953,261 , GRCh38.p12 chr2: 241,013,844-241,013,844 , GRCh38.p12 chr2: 241,013,943-241,013,943 SNED1-AS1, SNED1
    nsv5311767copy number variation1nstd204human GRCh38.p13 chr2: 240,919,346-241,591,263 , GRCh37.p13 chr2: 241,858,763-242,530,678 , LOC105373971, 25 more genes
    nsv5217593copy number variation1nstd204human GRCh38.p13 chr2: 241,021,206-241,038,851 , GRCh37.p13 chr2: 241,960,623-241,978,268 SNED1, SNED1-AS1
    nsv4914158copy number variation1nstd200human GRCh38 chr2: 241,016,319-241,026,307 , GRCh37.p13 chr2: 241,955,736-241,965,724 SNED1, SNED1-AS1
    nsv4914156copy number variation1nstd200human GRCh38 chr2: 240,919,601-241,590,939 , GRCh37.p13 chr2: 241,859,018-242,530,354 , LOC112268440, 25 more genes
    nsv4910449copy number variation1nstd200human GRCh38 chr2: 241,011,061-241,015,883 , GRCh37.p13 chr2: 241,950,478-241,955,300 SNED1-AS1, LOC107985787, 1 more genes
    nsv4804742copy number variation1nstd200human GRCh37 chr2: 241,859,018-242,530,357 , GRCh38.p12 chr2: 240,919,601-241,590,942 , MIR3133, 25 more genes
    nsv4768328copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,110,452-243,028,452 , GRCh38.p12 chr2: 232,245,742-242,086,301 LOC107985836, LOC105373980, 217 more genes
    nsv4757775insertion1nstd199human GRCh37 chr2: 241,955,048-241,955,048 , GRCh38.p12 chr2: 241,015,631-241,015,631 SNED1, SNED1-AS1
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4723343insertion1nstd186human GRCh37 chr2: 241,955,464-241,955,464 , GRCh38.p12 chr2: 241,016,047-241,016,047 SNED1, SNED1-AS1
    nsv4684239copy number variation1nstd102humanUncertain significance GRCh37 chr2: 238,863,455-243,048,760 , GRCh38.p12 chr2: 237,954,813-242,106,609 LOC285191, MTERF4, 103 more genes
    nsv4684149copy number variation1nstd102humanUncertain significance GRCh37 chr2: 241,791,028-242,842,568 , GRCh38.p12 chr2: 240,851,611-241,900,417 LOC105373978, ANO7, 39 more genes
    nsv4684141copy number variation1nstd102humanUncertain significance GRCh37 chr2: 241,810,850-243,048,760 , GRCh38.p12 chr2: 240,871,433-242,106,609 LOC105373974, LINC01238, 44 more genes
    nsv4682411copy number variation1nstd102humanPathogenic GRCh37 chr2: 241,808,273-242,708,241 , GRCh38.p12 chr2: 240,868,856-241,768,826 MIR3133, SNED1, 30 more genes
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