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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977326inversion1nstd209human GRCh38 chr5: 176,286,704-177,635,736 , GRCh37.p13 chr5: 175,713,707-177,062,737 , CLTB, 46 more genes
    nsv5892986copy number variation1nstd209human GRCh38 chr5: 177,435,913-177,441,610 , GRCh37.p13 chr5: 176,862,914-176,868,611 PRR7-AS1, GRK6
    nsv5890062copy number variation1nstd209human GRCh38 chr5: 176,061,658-178,007,127 , GRCh37.p13 chr5: 175,488,661-177,434,128 , DBN1, 65 more genes
    nsv5841620copy number variation1nstd209human GRCh38 chr5: 177,434,181-177,441,292 , GRCh37.p13 chr5: 176,861,182-176,868,293 PRR7-AS1, GRK6
    nsv5232677copy number variation1nstd204human GRCh38.p13 chr5: 177,340,901-177,518,700 , GRCh37.p13 chr5: 176,767,902-176,945,701 , FAM193B, 13 more genes
    nsv4826039copy number variation1nstd200human GRCh37 chr5: 176,863,322-176,863,564 , GRCh38.p12 chr5: 177,436,321-177,436,563 GRK6, PRR7-AS1
    nsv4826038copy number variation1nstd200human GRCh37 chr5: 176,862,916-176,868,612 , GRCh38.p12 chr5: 177,435,915-177,441,611 PRR7-AS1, GRK6
    nsv4768375copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,805,664-180,719,789 , GRCh38.p12 chr5: 171,378,660-181,292,788 LINC01863, PRDX2P3, 279 more genes
    nsv4765127inversion1nstd199human GRCh37 chr5: 175,457,760-177,239,501 , GRCh38.p12 chr5: 176,030,757-177,812,500 , CLTB, 60 more genes
    nsv4764354inversion1nstd199human GRCh37 chr5: 175,368,726-177,329,050 , GRCh38.p12 chr5: 175,941,723-177,902,049 , CLTB, 66 more genes
    nsv4763538inversion1nstd199human GRCh37 chr5: 170,260,689-178,183,120 , GRCh38.p12 chr5: 170,833,685-178,756,119 , BNIP1, 194 more genes
    nsv4763338inversion1nstd199human GRCh37 chr5: 175,460,977-177,237,065 , GRCh38.p12 chr5: 176,033,974-177,810,064 , CLTB, 60 more genes
    nsv4755941inversion1nstd199human GRCh37 chr5: 175,346,194-177,347,044 , GRCh38.p12 chr5: 175,919,191-177,920,043 , CLTB, 66 more genes
    nsv4729600copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,570,677-177,114,151 , GRCh38.p12 chr5: 176,143,674-177,687,150 RNF44, NOP16, 48 more genes
    nsv4729439copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,394,616-177,436,413 , GRCh38.p12 chr5: 175,967,613-178,009,412 KIAA1191, DOK3, 65 more genes
    nsv4685982copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,346,695-177,469,711 , GRCh38.p12 chr5: 175,919,692-178,042,710 NOP16, DDX41, 65 more genes
    nsv4592922copy number variation1nstd183human GRCh37 chr5: 176,776,426-176,946,576 , GRCh38.p12 chr5: 177,349,425-177,519,575 , PRR7, 12 more genes
    nsv4590638copy number variation1nstd183human GRCh37 chr5: 176,873,819-176,884,736 , GRCh38.p12 chr5: 177,446,818-177,457,735 DBN1, PRR7-AS1, 1 more genes
    nsv4457212copy number variation1nstd102humanUncertain significance GRCh37 chr5: 176,643,613-179,085,551 , GRCh38.p12 chr5: 177,216,612-179,658,550 LOC100502572, PIGFP1, 79 more genes
    nsv4457123copy number variation1nstd102humanUncertain significance GRCh37 chr5: 176,774,402-177,064,884 , GRCh38.p12 chr5: 177,347,401-177,637,883 RGS14, TMED9, 15 more genes
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