ifitm1[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7137204	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 268,586-748,873 , GRCh38.p12 chr11: 268,586-748,873	IFITM1, PKP3, 32 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	IFITM1, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	IFITM1, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	IFITM1, IGHMBP2, 2829 more genes
nsv3898926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-37,698,540 , GRCh38.p12 chr11: 230,615-37,676,990	IFITM1, OR51L1, 771 more genes
nsv4674879	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449	IFITM1, BGLT3, 723 more genes
nsv3906221	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673	IFITM1, PCNAP4, 688 more genes
nsv6315535	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599	IFITM1, OR52Q1P, 630 more genes
nsv3894525	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-25,584,362 , GRCh38.p12 chr11: 230,615-25,562,816	IFITM1, SDHCP4, 620 more genes
nsv3898948	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-17,099,213 , GRCh38.p12 chr11: 230,615-17,077,666	IFITM1, MTND5P21, 506 more genes
nsv4350476	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589	IFITM1, KRTAP5-3, 457 more genes
nsv3919565	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 61,793-10,727,969 , GRCh37 chr11: 61,793-10,749,516 , NCBI36 chr11: 51,793-10,706,092	IFITM1, OR51A7, 437 more genes
nsv3892294	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-9,704,511 , GRCh38.p12 chr11: 230,615-9,682,964	IFITM1, MRPS24P1, 405 more genes
nsv4768373	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811	IFITM1, LOC107984302, 375 more genes
nsv6637864	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177	IFITM1, PNPLA2, 372 more genes
nsv3918376	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 128,203-5,440,733 , GRCh37.p13 chr11: 138,203-5,484,157 , GRCh38.p12 chr11: 138,203-5,462,927	IFITM1, HBG2, 262 more genes
nsv3913735	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 196,855-5,343,104 , GRCh38 chr11: 196,855-5,321,874 , NCBI36 chr11: 186,855-5,299,680	IFITM1, CDKN1C, 246 more genes
nsv3894576	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 193,187-5,291,338 , GRCh38.p12 chr11: 193,187-5,270,108	IFITM1, SSU72L4, 243 more genes
nsv4729112	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307	IFITM1, OR51E1, 203 more genes
nsv3916105	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 186,966-4,413,150 , GRCh38 chr11: 196,966-4,435,344 , GRCh37 chr11: 196,966-4,456,574	IFITM1, MRPL23, 181 more genes

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Send to:

Search results

Items: 1 to 20 of 38

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 38

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity