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Items: 1 to 20 of 266

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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
    nsv7088580copy number variation1nstd229human GRCh38 chrX: 70,114,701-70,127,400 , GRCh37.p13 chrX: 69,334,551-69,347,250 MTND4P31, MTND6P31, 1 more genes
    nsv7088578copy number variation1nstd229human GRCh38 chrX: 70,104,539-70,128,503 , GRCh37.p13 chrX: 69,324,389-69,348,353 MTND6P31, MTND4P31, 1 more genes
    nsv7088572copy number variation1nstd229human GRCh38 chrX: 70,051,045-70,310,152 , GRCh37.p13 chrX: 69,270,895-69,530,002 MTND4P31, PDZD11, 13 more genes
    nsv7035676inversion1nstd229human GRCh38 chrX: 70,118,350-70,127,361 , GRCh37.p13 chrX: 69,338,200-69,347,211 MTND6P31, MTND4P31, 1 more genes
    nsv7032490inversion1nstd229human GRCh38 chrX: 69,948,785-70,257,134 , GRCh37.p13 chrX: 69,168,635-69,476,984 RN7SL581P, MTND5P39, 12 more genes
    nsv6636375copy number variation1nstd102humanUncertain significance GRCh37 chrX: 69,216,192-69,529,923 , GRCh38.p12 chrX: 69,996,342-70,310,073 RN7SL581P, MTND5P39, 16 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
    nsv6137629copy number variation1nstd213human GRCh37 chrX: 66,030,000-152,230,001 , GRCh38.p12 chrX: 66,810,158-153,061,271 ABCB7, AGTR2, 1162 more genes
    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
    nsv6137403copy number variation1nstd213human GRCh37 chrX: 61,730,000-103,250,001 , GRCh38.p12 chrX: 62,510,530-103,995,433 ABCB7, AR, 529 more genes
    nsv6137224copy number variation1nstd213human GRCh37 chrX: 69,240,000-69,560,001 , GRCh38.p12 chrX: 70,020,150-70,340,151 ARR3, EDA, 16 more genes
    nsv6137221copy number variation1nstd213human GRCh37 chrX: 66,020,000-152,230,001 , GRCh38.p12 chrX: 66,800,158-153,061,271 ABCB7, AGTR2, 1162 more genes
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