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Items: 1 to 20 of 341

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097553copy number variation1nstd102humanPathogenic GRCh37 chr5: 94,800,311-96,107,383 , GRCh38.p12 chr5: 95,464,607-96,771,679 LOC105379675, GPR150, 27 more genes
    nsv7058036inversion1nstd229human GRCh38 chr5: 94,195,543-97,660,538 , GRCh37.p13 chr5: 93,531,248-96,996,242 RIOK2, SPATA9, 51 more genes
    nsv7045134inversion1nstd229human GRCh38 chr5: 95,722,347-95,722,397 , GRCh37.p13 chr5: 95,058,051-95,058,101 SPATA9, RHOBTB3
    nsv7044198inversion1nstd229human GRCh38 chr5: 93,856,097-99,790,151 , GRCh37.p13 chr5: 93,191,803-99,125,855 FAM81B, LOC107986365, 78 more genes
    nsv7038569inversion1nstd229human GRCh38 chr5: 95,597,682-95,673,975 , GRCh37.p13 chr5: 94,933,386-95,009,679 SPATA9, GPR150, 4 more genes
    nsv6776649copy number variation1nstd229human GRCh38 chr5: 95,618,905-95,650,633 , GRCh37.p13 chr5: 94,954,609-94,986,337 LOC112267933, RFESD, 2 more genes
    nsv6775072copy number variation1nstd229human GRCh38 chr5: 95,636,329-95,655,196 , GRCh37.p13 chr5: 94,972,033-94,990,900 SPATA9, RFESD
    nsv6774065copy number variation1nstd229human GRCh38 chr5: 95,710,248-95,710,362 , GRCh37.p13 chr5: 95,045,952-95,046,066 SPATA9
    nsv6773004copy number variation1nstd229human GRCh38 chr5: 94,767,305-97,708,544 , GRCh37.p13 chr5: 94,103,010-97,044,248 FABP5P5, SPATA9, 45 more genes
    nsv6768734copy number variation1nstd229human GRCh38 chr5: 95,438,101-95,691,400 , GRCh37.p13 chr5: 94,773,805-95,027,104 RFESD, LOC112267933, 8 more genes
    nsv6767196copy number variation1nstd229human GRCh38 chr5: 95,464,994-96,106,661 , GRCh37.p13 chr5: 94,800,698-95,442,365 ELL2, ARSK, 19 more genes
    nsv6764067copy number variation1nstd229human GRCh38 chr5: 95,644,582-95,694,300 , GRCh37.p13 chr5: 94,980,286-95,030,004 SPATA9, RFESD, 1 more genes
    nsv6763127copy number variation1nstd229human GRCh38 chr5: 95,710,508-95,715,092 , GRCh37.p13 chr5: 95,046,212-95,050,796 SPATA9, RHOBTB3
    nsv6636846copy number variation1nstd102humanUncertain significance GRCh37 chr5: 93,524,163-95,017,463 , GRCh38.p12 chr5: 94,188,458-95,681,759 SPATA9, LOC105379089, 19 more genes
    nsv6410812copy number variation1nstd223human GRCh38 chr5: 95,381,684-95,927,497 , GRCh37.p13 chr5: 94,717,388-95,263,201 SKIC3, ARSK, 17 more genes
    nsv6409343copy number variation1nstd223human GRCh38 chr5: 95,636,329-95,655,196 , GRCh37.p13 chr5: 94,972,033-94,990,900 RFESD, SPATA9
    nsv6400634copy number variation1nstd223human GRCh38 chr5: 95,706,601-95,712,200 , GRCh37.p13 chr5: 95,042,305-95,047,904 RHOBTB3, SPATA9
    nsv6400108copy number variation1nstd223human GRCh38 chr5: 95,672,125-95,672,719 , GRCh37.p13 chr5: 95,007,829-95,008,423 SPATA9, LOC105379090
    nsv6399548copy number variation1nstd223human GRCh38 chr5: 95,659,432-95,660,048 , GRCh37.p13 chr5: 94,995,136-94,995,752 SPATA9
    nsv6313580copy number variation1nstd102humanPathogenic GRCh37 chr5: 93,650,000-114,969,108 , GRCh38.p12 chr5: 94,314,295-115,633,411 FER, HMGN1P15, 222 more genes
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