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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048230inversion1nstd229human GRCh38 chr4: 149,781,104-157,324,460 , GRCh37.p13 chr4: 150,702,256-158,245,612 LOC107986197, LINC02273, 119 more genes
    nsv7046905inversion1nstd229human GRCh38 chr4: 151,269,540-154,434,057 , GRCh37.p13 chr4: 152,190,692-155,355,209 GATB, LOC105377492, 47 more genes
    nsv6755165copy number variation1nstd229human GRCh38 chr4: 153,395,713-154,001,169 , GRCh37.p13 chr4: 154,316,865-154,922,321 TMEM131L, LOC101927947, 8 more genes
    nsv6748651copy number variation1nstd229human GRCh38 chr4: 153,597,982-153,813,178 , GRCh37.p13 chr4: 154,519,134-154,734,330 TLR2, TMEM131L, 6 more genes
    nsv6747519copy number variation1nstd229human GRCh38 chr4: 153,700,825-153,701,388 , GRCh37.p13 chr4: 154,621,977-154,622,540 TLR2
    nsv6746031copy number variation1nstd229human GRCh38 chr4: 153,710,348-153,722,275 , GRCh37.p13 chr4: 154,631,500-154,643,427 LOC105377499, RNF175, 1 more genes
    nsv6743931copy number variation1nstd229human GRCh38 chr4: 153,687,117-153,702,821 , GRCh37.p13 chr4: 154,608,269-154,623,973 TLR2
    nsv6742495copy number variation1nstd229human GRCh38 chr4: 153,633,533-154,349,873 , GRCh37.p13 chr4: 154,554,685-155,271,025 TLR2, RNF175, 7 more genes
    nsv6629377copy number variation1nstd224human GRCh37 chr4: 154,245,247-155,071,789 , GRCh38.p12 chr4: 153,324,095-154,150,637 TLR2, TMEM131L, 10 more genes
    nsv6572617inversion1nstd223human GRCh38 chr4: 151,269,541-154,434,055 , GRCh37.p13 chr4: 152,190,693-155,355,207 LOC107986197, LOC100419170, 47 more genes
    nsv6393764copy number variation1nstd223human GRCh38 chr4: 153,681,401-153,686,700 , GRCh37.p13 chr4: 154,602,553-154,607,852 TLR2, LOC100419170
    nsv6386013copy number variation1nstd223human GRCh38 chr4: 153,710,348-153,722,272 , GRCh37.p13 chr4: 154,631,500-154,643,424 TLR2, RNF175, 1 more genes
    nsv6378782copy number variation1nstd223human GRCh38 chr4: 153,395,713-154,001,208 , GRCh37.p13 chr4: 154,316,865-154,922,360 LOC100419170, LOC105377499, 8 more genes
    nsv6292472mobile element insertion1nstd186human GRCh37 chr4: 154,631,032-154,631,083 , GRCh38.p12 chr4: 153,709,880-153,709,931 TLR2, RNF175
    nsv6279668insertion1nstd214human GRCh38 chr4: 153,684,832-153,684,832 , GRCh37.p13 chr4: 154,605,984-154,605,984 TLR2
    nsv6135297copy number variation1nstd213human GRCh37 chr4: 148,450,000-155,050,001 , GRCh38.p12 chr4: 147,528,848-154,128,849 ANXA2P1, ASS1P8, 86 more genes
    nsv6134911copy number variation1nstd213human GRCh37 chr4: 147,270,000-190,610,001 , GRCh38.p12 chr4: 146,348,848-189,688,847 , AGA, 517 more genes
    nsv6134884copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,720,001 , GRCh38.p12 chr4: 108,308,844-160,798,849 , ANK2, 616 more genes
    nsv6134731copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,710,001 , GRCh38.p12 chr4: 108,308,844-160,788,849 , ANK2, 616 more genes
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
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