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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
    nsv7081704copy number variation1nstd229human GRCh38 chrX: 89,920,633-89,921,150 , GRCh37.p13 chrX: 89,175,632-89,176,149 TGIF2LX
    nsv7044698inversion1nstd229human GRCh38 chrX: 87,352,100-90,785,855 , GRCh37.p13 chrX: 86,607,103-90,040,854 UBE2V1P9, MRPS22P1, 15 more genes
    nsv6636889copy number variation1nstd102humanUncertain significance GRCh37 chrX: 87,082,472-95,826,084 , GRCh38.p12 chrX: 87,827,472-96,571,085 PABPC5-AS1, KAT7P1, 57 more genes
    nsv6634329copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,794,355-119,282,836 , GRCh38.p12 chrX: 77,538,874-120,148,930 NXF4, RHOXF1P1, 489 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
    nsv6290213copy number variation1nstd102humanPathogenic GRCh37 chrX: 88,361,395-99,758,442 , GRCh38.p12 chrX: 89,106,394-100,503,445 LOC107985647, CCNB1IP1P3, 70 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
    nsv6137409copy number variation1nstd213human GRCh37 chrX: 73,710,000-151,990,001 , GRCh38.p12 chrX: 74,490,165-152,821,457 ABCB7, AGTR2, 991 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
    nsv6137226copy number variation1nstd213human GRCh37 chrX: 71,050,000-104,350,001 , GRCh38.p12 chrX: 71,830,150-105,105,319 ABCB7, ATP7A, 394 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
    nsv6137215copy number variation3nstd213human GRCh37 chrX: 61,730,000-152,230,001 , GRCh38.p12 chrX: 62,510,530-153,061,271 ABCB7, AGTR2, 1217 more genes
    nsv6137213copy number variation1nstd213human GRCh37 chrX: 52,570,000-152,220,001 , GRCh38.p12 chrX: 52,729,004-152,738,707 ABCB7, ACTG1P10, 1298 more genes
    nsv6136791copy number variation1nstd213human GRCh37 chrX: 61,730,000-134,860,001 , GRCh38.p12 chrX: 62,510,530-135,719,285 ABCB7, AGTR2, 967 more genes
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