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Items: 1 to 20 of 328

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098869copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,586,015-154,774,957 , GRCh38.p12 chrX: 140,503,850-155,545,296 MAGEA6, LOC101928832, 303 more genes
    nsv7084572copy number variation1nstd229human GRCh38 chrX: 143,629,007-143,806,556 , GRCh37.p13 chrX|NW_004070889.1: 417,728-595,277 , GRCh37.p13 chrX: 142,716,823-142,889,651 SPANXN2, HNRNPH1P2, 1 more genes
    nsv7084569copy number variation1nstd229human GRCh38 chrX: 143,579,137-143,754,561 , GRCh37.p13 chrX|NW_004070889.1: 367,858-543,282 , GRCh37.p13 chrX: 142,666,963-142,837,656 SLITRK4, SPANXN2, 2 more genes
    nsv7084540copy number variation1nstd229human GRCh38 chrX: 143,385,405-143,993,512 , GRCh37.p13 chrX|NW_004070889.1: 174,126-782,233 , GRCh37.p13 chrX: 142,473,198-143,076,618 MTND1P33, MYCLP3, 6 more genes
    nsv7084521copy number variation1nstd229human GRCh38 chrX: 143,228,094-143,749,219 , GRCh37.p13 chrX|NW_004070889.1: 16,815-537,940 , GRCh37.p13 chrX: 142,315,880-142,832,314 SLITRK4, MTND1P33, 6 more genes
    nsv7079098copy number variation1nstd229human GRCh38 chrX: 139,214,744-145,647,139 , GRCh37.p13 chrX: 138,296,906-142,299,065 LOC101928833, ATP11C, 61 more genes
    nsv7053159inversion1nstd229human GRCh38 chrX: 143,356,368-146,168,320 , GRCh37.p13 chrX|NW_004070890.2: 1-1,692,711 , GRCh37.p13 chrX: 142,444,161-145,249,838 MIR888, MIR890, 22 more genes
    nsv6637060copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,510,129-145,119,351 , GRCh38.p12 chrX: 140,427,964-146,037,833 LOC101928833, MIR891A, 55 more genes
    nsv6637054copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,493,806-148,855,992 , GRCh38.p12 chrX: 140,411,641-149,774,334 SPANXN4, RRM2P4, 109 more genes
    nsv6636749copy number variation1nstd102humanUncertain significance GRCh37 chrX: 142,414,024-143,403,932 , GRCh38.p12 chrX: 143,326,229-144,320,823 SPANXN3, MTND2P39, 8 more genes
    nsv6636431copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,504,564-149,382,013 , GRCh38.p12 chrX: 140,422,399-150,213,783 MTND1P33, MIR514A1, 119 more genes
    nsv6636407copy number variation1nstd102humanPathogenic GRCh37 chrX: 124,749,464-155,233,731 , GRCh38.p12 chrX: 125,615,468-156,004,066 RN7SKP31, LOC728470, 539 more genes
    nsv6634391copy number variation1nstd102humanPathogenic GRCh37 chrX: 142,401,540-155,233,731 , GRCh38.p12 chrX: 143,313,746-156,004,066 CSAG4, LOC112268308, 279 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315429copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,670,699-155,233,731 , GRCh38.p12 chrX: 78,415,202-156,004,066 H2AB1, GPR174, 1081 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
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