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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054609inversion1nstd229human GRCh38 chr4: 95,257,712-104,152,159 , GRCh37.p13 chr4: 96,178,863-105,073,316 SLC39A8, PABPC1P7, 96 more genes
    nsv7052845inversion1nstd229human GRCh38 chr4: 97,450,222-102,053,198 , GRCh37.p13 chr4: 98,371,373-102,974,355 RNU6-462P, LOC105377345, 58 more genes
    nsv7052661inversion1nstd229human GRCh38 chr4: 96,912,053-103,991,076 , GRCh37.p13 chr4: 97,833,204-104,912,233 MIR1255A, LOC107986297, 86 more genes
    nsv7048086inversion1nstd229human GRCh38 chr4: 100,058,481-107,564,371 , GRCh37.p13 chr4: 100,979,638-108,485,528 ACTR6P1, INTS12, 79 more genes
    nsv7046928inversion1nstd229human GRCh38 chr4: 95,051,434-103,882,549 , GRCh37.p13 chr4: 95,972,585-104,803,706 PABPC1P7, RN7SL728P, 95 more genes
    nsv7044544inversion1nstd229human GRCh38 chr4: 98,964,941-108,185,877 , GRCh37.p13 chr4: 99,886,092-109,107,033 LOC102725220, TACR3, 117 more genes
    nsv6750884copy number variation1nstd229human GRCh38 chr4: 100,805,301-100,812,000 , GRCh37.p13 chr4: 101,726,458-101,733,157 LINC01218
    nsv6749924copy number variation1nstd229human GRCh38 chr4: 100,813,870-100,814,211 , GRCh37.p13 chr4: 101,735,027-101,735,368 LINC01218
    nsv6749088copy number variation1nstd229human GRCh38 chr4: 100,805,377-100,866,737 , GRCh37.p13 chr4: 101,726,534-101,787,894 LINC01218
    nsv6745006copy number variation1nstd229human GRCh38 chr4: 100,814,768-100,830,660 , GRCh37.p13 chr4: 101,735,925-101,751,817 LINC01218
    nsv6297885copy number variation1nstd186human GRCh37 chr4: 101,450,128-101,973,754 , GRCh38.p12 chr4: 100,528,971-101,052,597 PPP3CA, LINC01216, 2 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291428copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 95,490,755-109,977,216 , GRCh38.p12 chr4: 94,569,604-109,056,060 ADH1A, ADH1B, 157 more genes
    nsv6135624copy number variation1nstd213human GRCh37 chr4: 94,300,000-108,550,001 , GRCh38.p12 chr4: 93,378,849-107,628,845 , ADH1A, 146 more genes
    nsv6135091copy number variation1nstd213human GRCh37 chr4: 94,310,000-108,550,001 , GRCh38.p12 chr4: 93,388,849-107,628,845 , ADH1A, 146 more genes
    nsv6134729copy number variation1nstd213human GRCh37 chr4: 101,030,000-101,850,001 , GRCh38.p12 chr4: 100,108,843-100,928,844 EMCN, DDIT4L, 5 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5462161copy number variation1nstd206human GRCh38 chr4: 100,528,971-101,052,597 , GRCh37.p13 chr4: 101,450,128-101,973,754 PPP3CA, LINC01218, 2 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
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