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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5630072insertion1nstd207human GRCh38 chr9: 101,358,929-101,358,929 , GRCh37.p13 chr9: 104,121,211-104,121,211 LOC100421197, BAAT
    nsv5539714insertion1nstd206human GRCh38 chr9: 101,358,929-101,358,929 , GRCh37.p13 chr9: 104,121,211-104,121,211 LOC100421197, BAAT
    nsv5485103copy number variation1nstd206human GRCh38 chr9: 101,368,878-101,371,361 , GRCh37.p13 chr9: 104,131,160-104,133,643 FYTTD1P1, BAAT
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4768951insertion1nstd186human GRCh37 chr9: 104,121,212-104,121,212 , GRCh38.p12 chr9: 101,358,930-101,358,930 BAAT, LOC100421197
    nsv4751675insertion1nstd199human GRCh37 chr9: 104,121,211-104,121,211 , GRCh38.p12 chr9: 101,358,929-101,358,929 , GRCh38.p12 chr9|NT_187578.1: 410,163-410,163 BAAT, LOC100421197
    nsv4728848copy number variation1nstd102humanUncertain significance GRCh37 chr9: 103,872,812-104,974,365 , GRCh38.p12 chr9: 101,110,530-102,212,083 RNF20, LOC105376184, 20 more genes
    nsv4684901insertion1nstd194human GRCh38.p12 chr9: 101,358,930-101,358,930 , GRCh37 chr9: 104,121,212-104,121,212 BAAT, LOC100421197
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 RPS26P37, MIR27B, 238 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4443626insertion1nstd175human GRCh37 chr9: 104,121,211-104,121,211 , GRCh38.p12 chr9: 101,358,929-101,358,929 , GRCh38.p12 chr9|NT_187578.1: 410,163-410,163 BAAT, LOC100421197
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4192131copy number variation1nstd166human GRCh37.p13 chr9: 104,131,160-104,133,643 , GRCh38.p12 chr9: 101,368,878-101,371,361 , GRCh38.p12 chr9|NT_187578.1: 429,669-432,152 FYTTD1P1, BAAT
    nsv4190342copy number variation1nstd166human GRCh37.p13 chr9: 104,111,252-104,120,897 , GRCh38.p12 chr9: 101,348,970-101,358,615 , GRCh38.p12 chr9|NT_187578.1: 400,218-409,849 TRMT112P4, BAAT, 1 more genes
    nsv4173036copy number variation1nstd166human GRCh37.p13 chr9: 104,135,500-104,139,501 , GRCh38.p12 chr9|NT_187578.1: 434,009-438,010 , GRCh38.p12 chr9: 101,373,218-101,377,219 FYTTD1P1, BAAT
    nsv3968228copy number variation1nstd168human GRCh38 chr9: 101,364,606-101,408,650 , GRCh37.p13 chr9: 104,126,888-104,170,932 BAAT, ZNF189, 2 more genes
    nsv3965731insertion1nstd168human GRCh38 chr9: 101,312,824-101,364,606 , GRCh37.p13 chr9: 104,075,106-104,126,888 BAAT, PLPPR1, 3 more genes
    nsv3943804insertion1nstd167human GRCh37 chr9: 104,121,211-104,121,211 , GRCh38.p12 chr9: 101,358,929-101,358,929 , GRCh38.p12 chr9|NT_187578.1: 410,163-410,163 BAAT, LOC100421197
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