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Items: 1 to 20 of 325

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7081404copy number variation1nstd229human GRCh38 chrX: 66,034,384-66,680,174 , GRCh37.p13 chrX: 65,254,226-65,900,016 VSIG4, HEPH, 7 more genes
    nsv7081403copy number variation1nstd229human GRCh38 chrX: 66,027,478-66,853,005 , GRCh37.p13 chrX: 65,247,320-66,072,847 EIF4BP9, RNU6-394P, 8 more genes
    nsv7081394copy number variation1nstd229human GRCh38 chrX: 65,928,713-66,251,745 , GRCh37.p13 chrX: 65,148,555-65,471,587 RBMXP5, MIR223, 4 more genes
    nsv7081380copy number variation1nstd229human GRCh38 chrX: 65,819,364-66,337,755 , GRCh37.p13 chrX: 65,039,206-65,557,597 VSIG4, RBMXP5, 5 more genes
    nsv7081339copy number variation1nstd229human GRCh38 chrX: 65,446,707-66,134,477 , GRCh37.p13 chrX: 64,666,587-65,354,319 NANOGP9, EIF4BP9, 11 more genes
    nsv7081326copy number variation1nstd229human GRCh38 chrX: 65,375,750-66,393,455 , GRCh37.p13 chrX: 64,595,630-65,613,297 ETF1P3, CCNYL5, 14 more genes
    nsv7035385inversion1nstd229human GRCh38 chrX: 65,826,727-66,542,202 , GRCh37.p13 chrX: 65,046,569-65,762,044 ATXN7L3P1, RBMXP5, 7 more genes
    nsv7026403inversion1nstd229human GRCh38 chrX: 65,931,182-66,705,341 , GRCh37.p13 chrX: 65,151,024-65,925,183 ATXN7L3P1, EDA2R, 9 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
    nsv6315332copy number variation1nstd102humanPathogenic GRCh37 chrX: 62,685,885-155,233,731 , GRCh38.p12 chrX: 63,466,005-156,004,066 MAGT1, TAFAZZIN, 1337 more genes
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6313346copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,974,855-79,123,671 , GRCh38.p12 chrX: 62,755,385-79,868,171 RPS7P14, RNY4P23, 280 more genes
    nsv6313230copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,877,278-79,123,671 , GRCh38.p12 chrX: 62,657,808-79,868,171 SSBL2P, LOC105373239, 280 more genes
    nsv6223394insertion1nstd214human GRCh38 chrX: 66,037,757-66,037,757 , GRCh37.p13 chrX: 65,257,599-65,257,599 VSIG4
    nsv6137626copy number variation1nstd213human GRCh37 chrX: 61,730,000-73,580,001 , GRCh38.p12 chrX: 62,510,530-74,360,166 AR, ARR3, 210 more genes
    nsv6137405copy number variation1nstd213human GRCh37 chrX: 65,000,000-66,020,001 , GRCh38.p12 chrX: 65,780,158-66,800,159 VSIG4, PKMP2, 12 more genes
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