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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148213copy number variation1nstd102humanPathogenic GRCh38 chr19: 54,152,129-54,161,358 , GRCh37.p13 chr19|NW_004166865.1: 126,496-135,725 TMC4, LOC102724273, 2 more genes
    nsv7069393inversion1nstd229human GRCh38 chr19: 53,026,789-54,633,410 , GRCh37.p13 chr19: 53,530,042-54,528,887 MIR512-2, LILRB3, 145 more genes
    nsv7065131inversion1nstd229human GRCh38 chr19: 52,267,822-54,176,069 , GRCh37.p13 chr19: 52,771,075-54,528,887 ERVV-1, NDUFA3, 149 more genes
    nsv7060687inversion1nstd229human GRCh38 chr19: 53,785,748-54,383,705 , GRCh37.p13 chr19|NW_004166865.1: 1-358,072 MBOAT7, VSTM1, 36 more genes
    nsv7015734copy number variation1nstd229human GRCh38 chr19: 54,137,921-54,138,130 , GRCh37.p13 chr19|NW_004166865.1: 112,288-112,497 CNOT3
    nsv7015631copy number variation1nstd229human GRCh38 chr19: 54,129,801-54,139,500 , GRCh37.p13 chr19|NW_004166865.1: 104,168-113,867 PRPF31, CNOT3
    nsv7011952copy number variation1nstd229human GRCh38 chr19: 54,108,801-54,140,300 , GRCh37.p13 chr19|NW_004166865.1: 83,168-114,667 TFPT, CNOT3, 1 more genes
    nsv7002766copy number variation1nstd229human GRCh38 chr19: 54,150,614-54,150,644 , GRCh37.p13 chr19|NW_004166865.1: 124,981-125,011 CNOT3, LOC102724273
    nsv6998385copy number variation1nstd229human GRCh38 chr19: 54,133,701-54,137,100 , GRCh37.p13 chr19|NW_004166865.1: 108,068-111,467 CNOT3
    nsv6599207inversion1nstd223human GRCh38 chr19: 53,839,120-54,950,754 , GRCh37.p13 chr19|NW_004166865.1: 1-925,122 FCAR, KIR2DL1, 64 more genes
    nsv6597416inversion1nstd223human GRCh38 chr19: 53,217,793-54,175,150 , GRCh37.p13 chr19: 53,721,046-54,528,887 CACNG7, MIR371B, 110 more genes
    nsv6530259copy number variation1nstd223human GRCh38 chr19: 54,076,630-54,265,819 , GRCh37.p13 chr19|NW_004166865.1: 50,997-240,186 LOC107985279, RNU6-1307P, 16 more genes
    nsv6310493copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,297,303-55,678,016 , GRCh38.p12 chr19|NT_187693.1: 134,805-894,467 , GRCh38.p12 chr19: 53,794,049-55,166,648 PRPF31, TSEN34, 80 more genes
    nsv6146752copy number variation1nstd206human GRCh38 chr19: 54,134,874-54,159,874 , GRCh37.p13 chr19|NW_004166865.1: 109,241-134,241 TMC4, LOC102724273, 2 more genes
    nsv6146635copy number variation1nstd206human GRCh38 chr19: 54,138,874-54,144,874 , GRCh37.p13 chr19|NW_004166865.1: 113,241-119,241 CNOT3, LOC102724273
    nsv6146333copy number variation1nstd206human GRCh38 chr19: 54,142,874-54,150,874 , GRCh37.p13 chr19|NW_004166865.1: 117,241-125,241 LOC102724273, CNOT3
    nsv6146236copy number variation1nstd206human GRCh38 chr19: 54,149,874-54,158,874 , GRCh37.p13 chr19|NW_004166865.1: 124,241-133,241 TMC4, LOC102724273, 2 more genes
    nsv5024921copy number variation1nstd200human GRCh38 chr19: 54,151,759-54,152,198 , GRCh37.p13 chr19|NW_004166865.1: 126,126-126,565 LOC102724273, CNOT3
    nsv5024916copy number variation1nstd200human GRCh38 chr19: 54,026,823-54,153,040 , GRCh37.p13 chr19|NW_004166865.1: 1,190-127,407 CNOT3, PRPF31, 6 more genes
    nsv4730034copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,334,195-56,434,037 , GRCh38.p12 chr19: 53,830,941-55,922,671 , GRCh38.p12 chr19|NT_187693.1: 1-1,066,800 , GRCh38.p12 chr19|NW_003571057.2: 1-1,091,841 , GRCh38.p12 chr19|NW_003571058.2: 1-1,066,390 , GRCh38.p12 chr19|NW_003571056.2: 1-1,064,304 KIR3DP1, NLRP9, 133 more genes
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