dbVar for Gene (Select 7352) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6122022	copy number variation	1	nstd186	human		GRCh37 chr11: 73,710,014-73,710,225 , GRCh38.p12 chr11: 73,998,969-73,999,180	UCP3
nsv5909690	copy number variation	1	nstd209	human		GRCh38 chr11: 73,998,980-73,999,167 , GRCh37.p13 chr11: 73,710,025-73,710,212	UCP3
nsv5659901	insertion	1	nstd207	human		GRCh38 chr11: 73,999,132-73,999,132 , GRCh37.p13 chr11: 73,710,177-73,710,177	UCP3
nsv5510719	copy number variation	1	nstd206	human		GRCh38 chr11: 73,998,969-73,999,180 , GRCh37.p13 chr11: 73,710,014-73,710,225	UCP3
nsv5390777	copy number variation	2	nstd186	human		GRCh37 chr11: 73,710,015-73,710,225 , GRCh38.p12 chr11: 73,998,970-73,999,180	UCP3
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	FAUP4, MMP7, 2031 more genes
nsv5304483	copy number variation	1	nstd204	human		GRCh38.p13 chr11: 73,998,970-73,999,180 , GRCh37.p13 chr11: 73,710,015-73,710,225	UCP3
nsv4989053	copy number variation	1	nstd200	human		GRCh38 chr11: 73,998,970-73,999,180 , GRCh37.p13 chr11: 73,710,015-73,710,225	UCP3
nsv4846588	copy number variation	1	nstd200	human		GRCh37 chr11: 73,705,293-73,715,955 , GRCh38.p12 chr11: 73,994,248-74,004,910	UCP3, LOC100421622
nsv4836982	copy number variation	1	nstd200	human		GRCh37 chr11: 73,710,015-73,710,225 , GRCh38.p12 chr11: 73,998,970-73,999,180	UCP3
nsv4762307	insertion	1	nstd199	human		GRCh37 chr11: 73,710,020-73,710,020 , GRCh38.p12 chr11: 73,998,975-73,998,975	UCP3
nsv4456614	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 73,395,712-73,788,461 , GRCh38.p12 chr11: 73,684,667-74,077,416	PAAF1, DNAJB13, 12 more genes
nsv4455639	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 73,128,157-73,788,461 , GRCh38.p12 chr11: 73,417,112-74,077,416	RAB6A, UCP2, 16 more genes
nsv4446390	insertion	1	nstd175	human		GRCh37 chr11: 73,710,014-73,710,014 , GRCh38.p12 chr11: 73,998,969-73,998,969	UCP3
nsv3931917	insertion	1	nstd167	human		GRCh37 chr11: 73,710,177-73,710,177 , GRCh38.p12 chr11: 73,999,132-73,999,132	UCP3
nsv3920330	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr11: 72,963,618-73,522,072 , GRCh38 chr11: 73,574,925-74,133,379 , GRCh37 chr11: 73,285,970-73,844,424	UCP3, LOC268276, 16 more genes
nsv3916301	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 71,928,796-77,064,521 , GRCh37 chr11: 71,639,842-76,751,808 , NCBI36 chr11: 71,317,490-76,453,216	RN7SL786P, LIPT2-AS1, 146 more genes
nsv3915804	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895	TPBGL, MAP6, 173 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	IGHMBP2, SYTL2, 2829 more genes
nsv3907532	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 73,444,963-73,777,547 , GRCh38.p12 chr11: 73,733,918-74,066,502	UCP2, DPPA4P3, 11 more genes

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Number of Variants: 20

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 114

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Number of Variants: 20

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