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Items: 1 to 20 of 725

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147907insertion1nstd232human GRCh37.p13 chr11: 47,765,714-47,765,714 , GRCh38.p12 chr11: 47,744,162-47,744,162 , GRCh38.p12 chr11|NW_019805496.1: 176,529-176,529 FNBP4
    nsv7141854insertion1nstd232human GRCh37.p13 chr11: 47,833,981-47,833,981 , GRCh38.p12 chr11: 47,812,429-47,812,429 , GRCh38.p12 chr11|NW_019805496.1: 244,796-244,796 NUP160
    nsv7138390copy number variation1nstd232human GRCh37.p13 chr11: 47,833,776-47,833,852 , GRCh38.p12 chr11: 47,812,224-47,812,300 , GRCh38.p12 chr11|NW_019805496.1: 244,591-244,667 NUP160
    nsv6621173copy number variation1nstd224human GRCh37 chr11: 47,656,236-47,776,214 , GRCh38.p12 chr11: 47,634,684-47,754,662 , GRCh38.p12 chr11|NW_019805496.1: 62,499-187,029 AGBL2, MTCH2, 1 more genes
    nsv6309222copy number variation1nstd102humanUncertain significance GRCh37 chr11: 47,603,620-47,606,033 , GRCh38.p12 chr11: 47,582,068-47,584,481 , GRCh38.p12 chr11|NW_019805496.1: 9,894-12,307 NDUFS3
    nsv6302419copy number variation1nstd186human GRCh37 chr11: 47,705,247-47,705,578 , GRCh38.p12 chr11|NW_019805496.1: 116,062-116,393 , GRCh38.p12 chr11: 47,683,695-47,684,026 AGBL2
    nsv6301301copy number variation1nstd186human GRCh37 chr11: 47,630,777-47,632,027 , GRCh38.p12 chr11: 47,609,225-47,610,475 , GRCh38.p12 chr11|NW_019805496.1: 37,051-38,301 MTCH2
    nsv6301041copy number variation1nstd186human GRCh37 chr11: 47,630,991-47,632,150 , GRCh38.p12 chr11: 47,609,439-47,610,598 , GRCh38.p12 chr11|NW_019805496.1: 37,265-38,424 MTCH2
    nsv6300930copy number variation1nstd186human GRCh37 chr11: 47,620,010-47,623,383 , GRCh38.p12 chr11|NW_019805496.1: 26,284-29,657 , GRCh38.p12 chr11: 47,598,458-47,601,831 0
    nsv6293031mobile element insertion1nstd186human GRCh37 chr11: 47,752,690-47,752,741 , GRCh38.p12 chr11|NW_019805496.1: 163,505-163,556 , GRCh38.p12 chr11: 47,731,138-47,731,189 FNBP4
    nsv6127156insertion1nstd186human GRCh37 chr11: 47,659,912-47,659,912 , GRCh38.p12 chr11: 47,638,360-47,638,360 , GRCh38.p12 chr11|NW_019805496.1: 66,178-66,178 MTCH2
    nsv5389560copy number variation2nstd186human GRCh37 chr11: 47,761,869-47,763,238 , GRCh38.p12 chr11|NW_019805496.1: 172,684-174,053 , GRCh38.p12 chr11: 47,740,317-47,741,686 FNBP4
    nsv5333528translocation1nstd200human GRCh37 chr11: 47,623,383-47,623,383 , GRCh37 chr11: 47,620,010-47,620,010 , GRCh38.p12 chr11|NW_019805496.1: 29,657-29,657 , GRCh38.p12 chr11: 47,598,458-47,598,458 , GRCh38.p12 chr11: 47,601,831-47,601,831 , GRCh38.p12 chr11|NW_019805496.1: 26,284-26,284 0
    nsv4848564copy number variation1nstd200human GRCh37 chr11: 47,606,392-47,607,205 , GRCh38.p12 chr11: 47,584,840-47,585,653 , GRCh38.p12 chr11|NW_019805496.1: 12,666-13,479 NDUFS3, FAM180B
    nsv4843251copy number variation1nstd200human GRCh37 chr11: 47,768,481-47,772,401 , GRCh38.p12 chr11: 47,746,929-47,750,849 , GRCh38.p12 chr11|NW_019805496.1: 179,296-183,216 FNBP4
    nsv4841891copy number variation1nstd200human GRCh37 chr11: 47,630,671-47,632,217 , GRCh38.p12 chr11: 47,609,119-47,610,665 , GRCh38.p12 chr11|NW_019805496.1: 36,945-38,491 MTCH2
    nsv4838600copy number variation1nstd200human GRCh37 chr11: 47,683,468-47,985,362 , GRCh38.p12 chr11: 47,661,916-47,963,810 , GRCh38.p12 chr11|NW_019805496.1: 94,283-279,705 NUP160, AGBL2, 4 more genes
    nsv4837207copy number variation1nstd200human GRCh37 chr11: 47,620,458-47,624,509 , GRCh38.p12 chr11: 47,598,906-47,602,957 , GRCh38.p12 chr11|NW_019805496.1: 26,732-30,783 MTCH2
    nsv4834632copy number variation1nstd200human GRCh37 chr11: 47,761,869-47,763,238 , GRCh38.p12 chr11|NW_019805496.1: 172,684-174,053 , GRCh38.p12 chr11: 47,740,317-47,741,686 FNBP4
    nsv4834309copy number variation1nstd200human GRCh37 chr11: 47,771,720-47,771,846 , GRCh38.p12 chr11: 47,750,168-47,750,294 , GRCh38.p12 chr11|NW_019805496.1: 182,535-182,661 FNBP4
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