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Items: 1 to 20 of 277

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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
    nsv7083709copy number variation1nstd229human GRCh38 chrX: 130,467,325-130,881,463 , GRCh37.p13 chrX: 129,601,299-130,015,437 SPRING1P2, ENOX2, 4 more genes
    nsv7083706copy number variation1nstd229human GRCh38 chrX: 130,425,150-130,586,311 , GRCh37.p13 chrX: 129,559,124-129,720,285 DENND10P1, LOC105373336, 1 more genes
    nsv7083704copy number variation1nstd229human GRCh38 chrX: 130,399,183-131,164,499 , GRCh37.p13 chrX: 129,533,157-130,298,473 ENOX2-AS1, LINC01201, 8 more genes
    nsv7083703copy number variation1nstd229human GRCh38 chrX: 130,379,069-130,808,643 , GRCh37.p13 chrX: 129,513,043-129,942,617 FSIP2LP, DENND10P1, 6 more genes
    nsv7050206inversion1nstd229human GRCh38 chrX: 130,371,007-132,177,030 , GRCh37.p13 chrX: 129,504,981-131,311,058 FSIP2LP, SLC25A14, 32 more genes
    nsv7042777inversion1nstd229human GRCh38 chrX: 127,009,007-134,341,039 , GRCh37.p13 chrX: 126,142,990-133,475,069 ELF4, TJAP1P1, 97 more genes
    nsv6636818copy number variation1nstd102humanUncertain significance GRCh37 chrX: 129,542,798-130,004,339 , GRCh38.p12 chrX: 130,408,824-130,870,365 FSIP2LP, DENND10P1, 5 more genes
    nsv6636622copy number variation1nstd102humanUncertain significance GRCh37 chrX: 129,533,578-130,299,562 , GRCh38.p12 chrX: 130,399,604-131,165,588 FSIP2LP, DENND10P1, 8 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
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634198copy number variation1nstd224human GRCh37 chrX: 129,603,836-129,729,304 , GRCh38.p12 chrX: 130,469,862-130,595,330 DENND10P1, FSIP2LP, 1 more genes
    nsv6633819copy number variation1nstd224human GRCh37 chrX: 129,518,496-130,450,360 , GRCh38.p12 chrX: 130,384,522-131,316,386 IGSF1, GPR119, 11 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
    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
    nsv6137584copy number variation1nstd213human GRCh37 chrX: 129,540,000-129,660,001 , GRCh38.p12 chrX: 130,406,026-130,526,027 RBMX2, DENND10P1, 2 more genes
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