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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146221insertion1nstd232human GRCh37.p13 chr6: 88,042,441-88,042,441 , GRCh38.p12 chr6: 87,332,723-87,332,723 SMIM8, LOC100421022
    nsv7055086inversion1nstd229human GRCh38 chr6: 87,339,750-87,339,794 , GRCh37.p13 chr6: 88,049,468-88,049,512 SMIM8
    nsv7043799inversion1nstd229human GRCh38 chr6: 86,180,462-87,365,811 , GRCh37.p13 chr6: 86,890,180-88,075,529 MTHFD2P2, C6orf163, 14 more genes
    nsv7039342inversion1nstd229human GRCh38 chr6: 86,041,090-92,871,248 , GRCh37.p13 chr6: 86,750,808-93,580,966 NDUFA5P9, AKIRIN2, 85 more genes
    nsv6810835copy number variation1nstd229human GRCh38 chr6: 87,232,136-87,423,747 , GRCh37.p13 chr6: 87,941,854-88,133,465 LOC100421022, ZNF292, 7 more genes
    nsv6808765copy number variation1nstd229human GRCh38 chr6: 87,317,215-87,322,890 , GRCh37.p13 chr6: 88,026,933-88,032,608 GJB7, SMIM8
    nsv6807349copy number variation1nstd229human GRCh38 chr6: 87,330,250-87,595,767 , GRCh37.p13 chr6: 88,039,968-88,305,485 RARS2, LOC100420741, 10 more genes
    nsv6806624copy number variation1nstd229human GRCh38 chr6: 87,183,695-87,462,783 , GRCh37.p13 chr6: 87,893,413-88,172,501 CFAP206, C6orf163, 9 more genes
    nsv6805567copy number variation1nstd229human GRCh38 chr6: 87,323,031-87,323,118 , GRCh37.p13 chr6: 88,032,749-88,032,836 GJB7, SMIM8
    nsv6802514copy number variation1nstd229human GRCh38 chr6: 87,341,665-87,351,323 , GRCh37.p13 chr6: 88,051,383-88,061,041 C6orf163, SMIM8
    nsv6799255copy number variation1nstd229human GRCh38 chr6: 87,182,699-87,383,500 , GRCh37.p13 chr6: 87,892,417-88,093,218 C6orf163, SMIM8, 4 more genes
    nsv6636656copy number variation1nstd102humanUncertain significance GRCh37 chr6: 86,098,133-88,663,964 , GRCh38.p12 chr6: 85,388,415-87,954,246 LINC02535, RPL7P27, 45 more genes
    nsv6634392copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297 MTHFD2P2, RPL7P27, 212 more genes
    nsv6406658copy number variation1nstd223human GRCh38 chr6: 87,338,270-87,338,741 , GRCh37.p13 chr6: 88,047,988-88,048,459 SMIM8
    nsv6401614copy number variation1nstd223human GRCh38 chr6: 87,323,031-87,323,118 , GRCh37.p13 chr6: 88,032,749-88,032,836 SMIM8, GJB7
    nsv6313857copy number variation1nstd102humanPathogenic GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492 LOC101928570, RNU4-72P, 288 more genes
    nsv6216261insertion4nstd214human GRCh38 chr6: 87,332,723-87,332,723 , GRCh37.p13 chr6: 88,042,441-88,042,441 SMIM8, LOC100421022
    nsv6173740copy number variation1nstd214human GRCh38 chr6: 87,323,031-87,323,117 , GRCh37.p13 chr6: 88,032,749-88,032,835 SMIM8, GJB7
    nsv6135938copy number variation1nstd213human GRCh37 chr6: 87,590,000-89,360,001 , GRCh38.p12 chr6: 86,880,282-88,650,282 ACTBP8, CGA, 33 more genes
    nsv6135855copy number variation1nstd213human GRCh37 chr6: 87,530,000-91,880,001 , GRCh38.p12 chr6: 86,820,282-91,170,283 ACTBP8, CGA, 67 more genes
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