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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096356copy number variation1nstd102humanUncertain significance GRCh37 chr22: 36,744,929-36,745,281 , GRCh38.p12 chr22: 36,348,884-36,349,236 MYH9
    nsv7098734copy number variation1nstd102humanUncertain significance GRCh37 chr22: 36,677,322-36,714,251 , GRCh38.p12 chr22: 36,281,276-36,318,206 MYH9, MIR6819
    nsv3906713copy number variation1nstd102humanBenign GRCh37 chr22: 36,611,863-36,714,089 , GRCh38.p12 chr22: 36,215,817-36,318,044 MYH9, APOL2, 2 more genes
    nsv3901878copy number variation1nstd102humanBenign GRCh37 chr22: 36,616,135-36,714,652 , GRCh38.p12 chr22: 36,220,089-36,318,607 MYH9, APOL1, 2 more genes
    nsv3904657copy number variation1nstd102humanBenign GRCh37 chr22: 36,616,135-36,713,869 , GRCh38.p12 chr22: 36,220,089-36,317,824 MYH9, APOL1, 2 more genes
    nsv3894607copy number variation1nstd102humanBenign GRCh37 chr22: 36,616,135-36,712,903 , GRCh38.p12 chr22: 36,220,089-36,316,858 MYH9, APOL1, 2 more genes
    nsv3902024copy number variation1nstd102humanBenign GRCh37 chr22: 36,614,056-36,710,183 , GRCh38.p12 chr22: 36,218,010-36,314,138 MYH9, APOL1, 2 more genes
    nsv3893763copy number variation2nstd102humanUncertain significance GRCh37 chr22: 36,614,412-36,716,248 , GRCh38.p12 chr22: 36,218,366-36,320,203 MYH9, APOL2, 2 more genes
    nsv3917534copy number variation1nstd102humanUncertain significance GRCh38 chr22: 36,218,250-36,311,777 , GRCh37 chr22: 36,614,296-36,707,822 , NCBI36 chr22: 34,944,242-35,037,768 MYH9, APOL1, 2 more genes
    nsv3924130copy number variation1nstd102humanUncertain significance GRCh37 chr22: 36,642,106-36,709,226 , GRCh38 chr22: 36,246,060-36,313,181 , NCBI36 chr22: 34,972,052-35,039,172 MYH9, APOL1, 1 more genes
    nsv7096355copy number variation1nstd102humanUncertain significance GRCh37 chr22: 36,651,002-36,710,383 , GRCh38.p12 chr22: 36,254,956-36,314,338 MYH9, MIR6819, 1 more genes
    nsv3896174copy number variation1nstd102humanUncertain significance GRCh37 chr22: 36,623,928-36,677,639 , GRCh38.p12 chr22: 36,227,882-36,281,593 MYH9, APOL1, 1 more genes
    nsv3907139copy number variation1nstd102humanUncertain significance GRCh37 chr22: 36,623,928-36,677,580 , GRCh38.p12 chr22: 36,227,882-36,281,534 MYH9, APOL1, 1 more genes
    nsv3922128copy number variation1nstd102humanPathogenic GRCh37 chr22: 35,729,986-39,296,182 , NCBI36 chr22: 34,059,986-37,626,128 , GRCh38 chr22: 35,333,993-38,900,177 MYH9, LOC102724378, 120 more genes
    nsv1398432copy number variation1nstd102humanPathogenic GRCh37 chr22: 35,680,095-38,098,981 , GRCh38.p12 chr22: 35,284,102-37,702,974 MYH9, MTCO1P20, 74 more genes
    nsv3902776copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,054,667-51,243,435 , GRCh38.p12 chr22: 16,367,190-50,805,007 MYH9, LOC100419811, 1084 more genes
    nsv3894026copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,054,691-51,237,518 , GRCh38.p12 chr22: 16,367,190-50,799,090 MYH9, IGKV3OR22-2, 1084 more genes
    nsv3890411copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,054,691-51,237,463 , GRCh38.p12 chr22: 16,367,190-50,799,035 MYH9, RNU6-495P, 1084 more genes
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 MYH9, FBXO7, 1084 more genes
    nsv3902598copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,054,691-51,220,902 , GRCh38.p12 chr22: 16,367,190-50,782,474 MYH9, FABP5P11, 1084 more genes
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