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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673809copy number variation1nstd102humanPathogenic GRCh37 chr8: 38,090,513-38,117,639 , GRCh38.p12 chr8: 38,232,995-38,260,121 DDHD2, PLPP5
    nsv5474516copy number variation1nstd206human GRCh38 chr8: 38,255,603-38,259,882 , GRCh37.p13 chr8: 38,113,121-38,117,400 PLPP5, DDHD2
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4954359copy number variation1nstd200human GRCh38 chr8: 38,198,435-38,308,758 , GRCh37.p13 chr8: 38,055,953-38,166,276 BAG4, DDHD2, 2 more genes
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4705929copy number variation1nstd195human GRCh37 chr8: 38,103,051-38,234,601 , GRCh38.p12 chr8: 38,245,533-38,377,083 DDHD2, NSD3, 1 more genes
    nsv4675476copy number variation1nstd102humanUncertain significance GRCh37 chr8: 38,045,946-38,348,258 , GRCh38.p12 chr8: 38,188,428-38,490,740 BAG4, LETM2, 6 more genes
    nsv4669328copy number variation1nstd186human GRCh37 chr8: 38,113,065-38,117,370 , GRCh38.p12 chr8: 38,255,547-38,259,852 DDHD2, PLPP5
    nsv4617568copy number variation1nstd183human GRCh37 chr8: 38,113,065-38,117,370 , GRCh38.p12 chr8: 38,255,547-38,259,852 PLPP5, DDHD2
    nsv4599995copy number variation1nstd183human GRCh37 chr8: 38,057,345-38,168,367 , GRCh38.p12 chr8: 38,199,827-38,310,849 NSD3, DDHD2, 2 more genes
    nsv4457098copy number variation1nstd102humanUncertain significance GRCh37 chr8: 38,057,332-38,167,170 , GRCh38.p12 chr8: 38,199,814-38,309,652 PLPP5, NSD3, 2 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4456199copy number variation1nstd102humanUncertain significance GRCh37 chr8: 36,094,421-43,822,214 , GRCh38.p12 chr8: 36,236,903-43,967,071 AFG3L2P1, BRF2, 136 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4163498copy number variation1nstd166human GRCh37.p13 chr8: 38,121,683-38,122,218 , GRCh38.p12 chr8: 38,264,165-38,264,700 PLPP5, DDHD2
    nsv4154693copy number variation1nstd166human GRCh37.p13 chr8: 38,123,764-38,124,370 , GRCh38.p12 chr8: 38,266,246-38,266,852 DDHD2, PLPP5
    nsv3968519copy number variation1nstd168human GRCh38 chr8: 38,151,809-38,273,991 , GRCh37.p13 chr8: 38,009,327-38,131,509 BAG4, DDHD2, 5 more genes
    nsv3924317copy number variation1nstd102humanPathogenic NCBI36 chr8: 38,042,602-40,318,326 , GRCh38 chr8: 38,065,927-40,341,650 , GRCh37 chr8: 37,923,445-40,199,169 RPL3P10, ADAM32, 37 more genes
    nsv3923517copy number variation1nstd102humanPathogenic NCBI36 chr8: 36,556,779-60,694,111 , GRCh37 chr8: 36,437,621-60,531,557 , GRCh38 chr8: 36,580,103-59,618,998 LOC105379380, TPT1P8, 320 more genes
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