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Items: 1 to 20 of 213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137210copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,943,184-76,085,232 , GRCh38.p12 chr15: 72,650,843-75,792,891 LOC105370892, MRPS15P1, 99 more genes
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7094304copy number variation1nstd102humanUncertain significance GRCh37 chr15: 72,978,569-75,190,071 , GRCh38.p12 chr15: 72,686,228-74,897,730 TBC1D21, LOC105370893, 60 more genes
    nsv7070270inversion1nstd229human GRCh38 chr15: 70,870,846-78,233,029 , GRCh37.p13 chr15: 71,163,185-78,525,371 GOLGA6C, LOC102723657, 178 more genes
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv7064472inversion1nstd229human GRCh38 chr15: 73,034,378-79,475,825 , GRCh37.p13 chr15: 73,326,719-79,768,167 ANP32BP1, PSTPIP1, 169 more genes
    nsv7062055inversion1nstd229human GRCh38 chr15: 72,671,162-80,404,440 , GRCh37.p13 chr15: 72,963,503-80,696,782 MIR184, TRK-CTT16-1, 194 more genes
    nsv7059031inversion1nstd229human GRCh38 chr15: 70,160,153-73,809,878 , GRCh37.p13 chr15: 70,452,492-74,102,219 CD276, LOC107984716, 71 more genes
    nsv7058635inversion1nstd229human GRCh38 chr15: 72,631,383-74,206,190 , GRCh37.p13 chr15: 72,923,724-74,498,531 COMMD4P2, PML, 38 more genes
    nsv6977744copy number variation1nstd229human GRCh38 chr15: 73,724,929-73,733,933 , GRCh37.p13 chr15: 74,017,270-74,026,274 INSYN1
    nsv6974819copy number variation1nstd229human GRCh38 chr15: 73,732,264-73,746,878 , GRCh37.p13 chr15: 74,024,605-74,039,219 INSYN1
    nsv6974760copy number variation1nstd229human GRCh38 chr15: 73,744,891-73,745,062 , GRCh37.p13 chr15: 74,037,232-74,037,403 INSYN1
    nsv6960714copy number variation1nstd229human GRCh38 chr15: 73,736,744-73,738,533 , GRCh37.p13 chr15: 74,029,085-74,030,874 INSYN1
    nsv6576038inversion1nstd223human GRCh38 chr15: 72,631,383-74,206,190 , GRCh37.p13 chr15: 72,923,724-74,498,531 ISLR, ISLR2, 38 more genes
    nsv6511773copy number variation1nstd223human GRCh38 chr15: 73,744,891-73,745,062 , GRCh37.p13 chr15: 74,037,232-74,037,403 INSYN1
    nsv6505595copy number variation1nstd223human GRCh38 chr15: 73,724,998-73,733,924 , GRCh37.p13 chr15: 74,017,339-74,026,265 INSYN1
    nsv6309803copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,103,084-74,244,178 , GRCh38.p12 chr15: 71,810,744-73,951,837 PHB1P20, TMEM202, 51 more genes
    nsv6309590copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,978,569-75,722,716 , GRCh38.p12 chr15: 72,686,228-75,430,375 NPM1P42, MAN2C1, 82 more genes
    nsv6202497copy number variation1nstd214human GRCh38 chr15: 73,744,891-73,745,061 , GRCh37.p13 chr15: 74,037,232-74,037,402 INSYN1
    nsv6133155copy number variation1nstd213human GRCh37 chr15: 72,730,000-102,440,001 , GRCh38.p12 chr15: 72,437,659-101,899,798 , BLM, 609 more genes
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